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Dayang Chem (Hangzhou) Co.,Ltd.

As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch

Trimethylaluminium Manufacturer/High quality/Best price/In stock

Cas:75-24-1

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

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Hebei yanxi chemical co.,LTD.

Hebei yanxi chemical co. LTD. has expanded a compositive entity from initially only as a small manufacturer. The company dedicated to the development, production and marketing of chemicals. After many years of efforts, we have established stable

Trimethylaluminium

Cas:75-24-1

Min.Order:1 Metric Ton

FOB Price: $1.0 / 2.0

Type:Manufacturers

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Henan Allgreen Chemical Co.,Ltd

high quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai

TriMethylaluMinuM;AluMinuMtriMeth-anide; ATM ;

Cas:75-24-1

Min.Order:1 Gram

Negotiable

Type:Manufacturers

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Ality Chemical Corporation

The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi

Factory Supply Trimethylaluminium

Cas:75-24-1

Min.Order:1

Negotiable

Type:Other

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Chemwill Asia Co., Ltd.

Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block

Trimethylaluminum

Cas:75-24-1

Min.Order:5 Kiloliter

FOB Price: $1.2 / 5.0

Type:Manufacturers

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Baoji Guokang Healthchem co.,ltd

Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present

Trimethylaluminium Organic aluminum

Cas:75-24-1

Min.Order:1 Kilogram

FOB Price: $6.0 / 10.0

Type:Trading Company

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Henan Wentao Chemical Product Co., Ltd.

Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod

CAS NO.:75-24-1

Cas:75-24-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Hangzhou Keyingchem Co.,Ltd

Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det

Three methyl aluminum

Cas:75-24-1

Min.Order:0 Metric Ton

Negotiable

Type:Lab/Research institutions

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Hangzhou J&H Chemical Co., Ltd.

J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia

Aluminum, trimethyl-

Cas:75-24-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai Massive Chemical Technology Co., Ltd.

Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and

Trimethylaluminium

Cas:75-24-1

Min.Order:1 Gram

FOB Price: $1.0

Type:Lab/Research institutions

inquiry

Zibo Hangyu Biotechnology Development Co., Ltd

Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi

Trimethylaluminum

Cas:75-24-1

Min.Order:10 Gram

FOB Price: $100.0

Type:Lab/Research institutions

inquiry

HANGZHOU YUNUO CHEMICAL CO.,LTD

Superior quality Appearance:clear colorless solution Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as catalysts for olefin polymerization,

Trimethylaluminium

Cas:75-24-1

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

inquiry

Henan Tianfu Chemical Co., Ltd.

Trimethylaluminium Chemical Properties Melting point 15 °C Boiling point 126 °C density 0.81 g/mL at 25 °C Fp 40 °F storage temp. 0-6°C solubility Soluble in arom

75-24-1 Trimethylaluminium

Cas:75-24-1

Min.Order:1 Metric Ton

FOB Price: $20.0

Type:Lab/Research institutions

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Hunan chemfish Pharmaceutical co.,Ltd

Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea

Trimethylaluminum

Cas:75-24-1

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

SAGECHEM LIMITED

SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe

Trimethylaluminium

Cas:75-24-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Kono Chem Co.,Ltd

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou

Trimethylaluminium

Cas:75-24-1

Min.Order:0

Negotiable

Type:Other

inquiry

Hangzhou Dingyan Chem Co., Ltd

R & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou

TriMethylaluMinuM

Cas:75-24-1

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

JINHUA HUAYI CHEMICAL CO., LTD.

Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands

Trimethylaluminium

Cas:75-24-1

Min.Order:100 Gram

Negotiable

Type:Lab/Research institutions

inquiry

Hunan Russell Chemicals Technology Co.,Ltd

low price and high purity Package:as customer required Application:ALD related industries,medicine and electronic materials

Trimethylaluminum

Cas:75-24-1

Min.Order:0 Metric Ton

Negotiable

Type:Trading Company

inquiry

Zhuozhou Wenxi import and Export Co., Ltd

Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

factory directly supply CAS 75-24-1 with competitive price

Cas:75-24-1

Min.Order:1 Kilogram

FOB Price: $112.0

Type:Trading Company

inquiry

Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

Aluminum, trimethyl-

Cas:75-24-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Xiamen AmoyChem Co.,Ltd

Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi

Trimethylaluminum

Cas:75-24-1

Min.Order:0

Negotiable

Type:Other

inquiry

Hubei Langyou International Trading Co., Ltd

75-24-1 Trimethylaluminium Application:75-24-1 Trimethylaluminium

75-24-1 Trimethylaluminium

Cas:75-24-1

Min.Order:0

Negotiable

Type:Other

inquiry

Hangzhou Fandachem Co.,Ltd

Trimethylaluminium cas 75-24-1Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

Trimethylaluminium cas 75-24-1

Cas:75-24-1

Min.Order:0

Negotiable

Type:Other

inquiry

Hangzhou ZeErRui Chemical Co., Ltd.

Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an

Triethylaluminum manufature

Cas:75-24-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Hunan Longxianng Runhui Trading Co.,Ltd

75-24-1 TrimethylaluminiumAppearance:powder Storage:room tempurature Package:As required Application:medical Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airport) or by sea LCL/FCL for large amo

75-24-1 Trimethylaluminium

Cas:75-24-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Chemsigma International Co.,Ltd.

bulk?production Application:Pharmaceutical intermediates

Trimethylaluminium

Cas:75-24-1

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Beantown Chemical

in stock Application:75-24-1

Trimethylaluminum solution, 25 wt. % in hexane

Cas:75-24-1

Min.Order:0

Negotiable

Type:Trading Company

inquiry

HWRK Chem

in storeAppearance:Liquid Package:100ml Application:Organic Chemicals

Trimethylaluminum

Cas:75-24-1

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Amadis Chemical Co., Ltd.

1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G

Amadis Chemical offer CAS#75-24-1;CAT#A838359

Cas:75-24-1

Min.Order:10 Milligram

Negotiable

Type:Lab/Research institutions

inquiry

Synthetic route

aluminium trichloride
7446-70-0

aluminium trichloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
With methylmagnesium bromide In not given react. of AlCl3 with MeMgBr;99%
gallium
7440-55-3

gallium

methyl aluminium sesquichloride

methyl aluminium sesquichloride

A

trimethylaluminum
75-24-1

trimethylaluminum

B

trimethyl gallium
1445-79-0

trimethyl gallium

Conditions
ConditionsYield
With methylene chloride; sodium at 40 - 50℃; under 375.038 Torr; Inert atmosphere; Flow reactor;A 93.7%
B 96.8%
triethylaluminum
97-93-8

triethylaluminum

aluminium
7429-90-5

aluminium

A

trimethylaluminum
75-24-1

trimethylaluminum

B

diethylaluminum iodide
2040-00-8

diethylaluminum iodide

Conditions
ConditionsYield
With iodine; methyl iodide In ethanol Sonication; N2; CH3I, I2 and Al introduced in a condenser with C2H5OH at -20°C, ultrasonic acceleration at room temp. for 2 h, Et3Al (ratio MeI/Et3Al = 1.50) dropped into soln. within 10 min, sonication for 30 min; distilled (vac.);A 86%
B 95%
neodymium tetramethylaluminate

neodymium tetramethylaluminate

2,4,6-tri-tert-butylbenzoic acid
66415-27-8

2,4,6-tri-tert-butylbenzoic acid

A

(Nd((2,4,6-tri-tert-butylbenzoate)[(μ-Me)2AlMe2]2)2

(Nd((2,4,6-tri-tert-butylbenzoate)[(μ-Me)2AlMe2]2)2

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In hexane; toluene byproducts: CH4; in a glovebox, Nd-contg. compd. (0.50 mmol) was dissolved in hexane, anda toluene suspn. of carboxylic acid (0.50 mmol) was slowly added; stirr ing at ambient temp. for 18 h; the solvent was removed in vac.; extn. in toluene; the complex was washed with hexane and dried for several hours; elem. anal.;A 94%
B n/a
triethylaluminum
97-93-8

triethylaluminum

aluminium
7429-90-5

aluminium

A

trimethylaluminum
75-24-1

trimethylaluminum

B

dimethyl aluminum iodide
2938-72-9

dimethyl aluminum iodide

C

ethyl aluminium iodide
2938-73-0

ethyl aluminium iodide

Conditions
ConditionsYield
With iodine; methyl iodide In ethanol Sonication; N2, CH3I, I2 and Al introduced in a condenser with C2H5OH at -20°C, ultrasonic acceleration at room temp. for 2 h, Et3Al (ratio MeI/Et3Al = 12.00) dropped into soln. within 10 min, sonicated for 30 min; distilled (vac.);A 62.5%
B 22.5%
C 93%
lanthanum tetramethylaluminate

lanthanum tetramethylaluminate

2,4,6-tri-tert-butylbenzoic acid
66415-27-8

2,4,6-tri-tert-butylbenzoic acid

A

(La((2,4,6-tri-tert-butylbenzoate)[(μ-Me)2AlMe2]2)2

(La((2,4,6-tri-tert-butylbenzoate)[(μ-Me)2AlMe2]2)2

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In hexane; toluene byproducts: CH4; in a glovebox, La-contg. compd. (0.50 mmol) was dissolved in hexane, anda toluene suspn. of carboxylic acid (0.50 mmol) was slowly added; stirr ing at ambient temp. for 18 h; the solvent was removed in vac.; extn. in toluene; the complex was washed with hexane and dried for several hours; elem. anal.;A 93%
B n/a
lanthanum tetramethylaluminate

lanthanum tetramethylaluminate

1,2,3,4,5-pentamethylcyclopentadiene
4045-44-7

1,2,3,4,5-pentamethylcyclopentadiene

A

(1,2,3,4,5-pentamethylcyclopentadienyl)bis(tetramethylaluminato)lanthanum(III)

(1,2,3,4,5-pentamethylcyclopentadienyl)bis(tetramethylaluminato)lanthanum(III)

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In hexane byproducts: CH4; Schlenk technique; diene (1 equiv.) in hexane was added with stirring tosoln. of La complex in hexane; mixt. was stirred for 5 min; solvent removed (vac.); dried (vac.); elem. anal.;A 93%
B n/a
neodymium tetramethylaluminate

neodymium tetramethylaluminate

1,2,3,4,5-pentamethylcyclopentadiene
4045-44-7

1,2,3,4,5-pentamethylcyclopentadiene

A

(1,2,3,4,5-pentamethylcyclopentadienyl)bis(tetramethylaluminato)neodymium(III)

(1,2,3,4,5-pentamethylcyclopentadienyl)bis(tetramethylaluminato)neodymium(III)

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In hexane byproducts: CH4; Schlenk technique; diene (1 equiv.) in hexane was added with stirring tosoln. of Nd complex in hexane; mixt. was stirred for 5 min; solvent removed (vac.); dried (vac.); elem. anal.;A 91%
B n/a
tris(η2-tetramethylaluminato)lutetium(III)

tris(η2-tetramethylaluminato)lutetium(III)

1,2,3,4,5-pentamethylcyclopentadiene
4045-44-7

1,2,3,4,5-pentamethylcyclopentadiene

A

(1,2,3,4,5-pentamethylcyclopentadienyl)bis(tetramethylaluminato)lutetium(III)

(1,2,3,4,5-pentamethylcyclopentadienyl)bis(tetramethylaluminato)lutetium(III)

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In hexane byproducts: CH4; Schlenk technique; diene (1 equiv.) in hexane was added with stirring tosoln. of Lu complex in hexane; mixt. was stirred for 5 min; solvent removed (vac.); dried (vac.); elem. anal.;A 91%
B n/a
tris(η2-tetramethylaluminato)yttrium(III)

tris(η2-tetramethylaluminato)yttrium(III)

2,4,6-tri-tert-butylbenzoic acid
66415-27-8

2,4,6-tri-tert-butylbenzoic acid

A

(Y((2,4,6-tri-tert-butylbenzoate)[(μ-Me)2AlMe2]2)2

(Y((2,4,6-tri-tert-butylbenzoate)[(μ-Me)2AlMe2]2)2

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In hexane; toluene byproducts: CH4; in a glovebox, Y-contg. compd. (0.50 mmol) was dissolved in hexane, and a toluene suspn. of carboxylic acid (0.50 mmol) was slowly added; stirring at ambient temp. for 18 h; the solvent was removed in vac.; extn. in toluene; the complex was washed with hexane and dried for several hours; elem. anal.;A 87%
B n/a
methylene chloride
74-87-3

methylene chloride

dimethylaluminum chloride
1184-58-3

dimethylaluminum chloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
With sodium; copper In Hexadecane at 20 - 130℃; under 825.083 - 862.586 Torr; for 2.2h; Inert atmosphere; Flow reactor;87%
With sodium In melt; 1,3,5-trimethyl-benzene at 100 - 120℃; under 7.50075 Torr; for 6h; Inert atmosphere;69.5 g
methylene chloride
74-87-3

methylene chloride

methylaluminum dichloride
917-65-7

methylaluminum dichloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
With sodium; gold In Hexadecane at 20 - 130℃; under 825.083 - 862.586 Torr; for 2.2h; Inert atmosphere; Flow reactor;87%
With sodium In melt; 1,3,5-trimethyl-benzene at 80 - 120℃; under 7.50075 Torr; for 8h; Inert atmosphere;68.4 g
methyl iodide
74-88-4

methyl iodide

methylaluminum sesquichloride

methylaluminum sesquichloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
Stage #1: methyl iodide With magnesium In diethyl ether at 15℃; for 1h; Inert atmosphere;
Stage #2: methylaluminum sesquichloride In pentane at 20℃; for 4h; Inert atmosphere;
87%
methylene chloride
74-87-3

methylene chloride

methylaluminum sesquichloride

methylaluminum sesquichloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
With silver; sodium In Hexadecane at 20 - 130℃; under 825.083 - 862.586 Torr; for 2.2h; Temperature; Inert atmosphere; Flow reactor;87%
tris(η2-tetramethylaluminato)yttrium(III)

tris(η2-tetramethylaluminato)yttrium(III)

1,2,3,4,5-pentamethylcyclopentadiene
4045-44-7

1,2,3,4,5-pentamethylcyclopentadiene

A

(1,2,3,4,5-pentamethylcyclopentadienyl)bis(tetramethylaluminato)yttrium(III)

(1,2,3,4,5-pentamethylcyclopentadienyl)bis(tetramethylaluminato)yttrium(III)

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In hexane byproducts: CH4; Schlenk technique; diene (1 equiv.) in hexane was added with stirring tosoln. of Y complex in hexane; mixt. was stirred for 5 min; solvent removed (vac.); dried (vac.); elem. anal.;A 86%
B n/a
(CH2)3(P(C6H5)2Al(CH3)3)2*2C6H6

(CH2)3(P(C6H5)2Al(CH3)3)2*2C6H6

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In neat (no solvent) metal complex decomposed at 120-140°C for 2-3 h;86%
triethylaluminum
97-93-8

triethylaluminum

aluminium
7429-90-5

aluminium

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
With iodine; methyl iodide In ethanol Sonication; N2, CH3I, I2 and Al introduced in a condenser with C2H5OH at -20°C, ultrasonic acceleration at room temp. for 2 h, Et3Al (ratio MeI/Et3Al = 0.75) dropped into soln. within 10 min, sonicated for 30 min; distilled (vac.);85%
methyl bromide
74-83-9

methyl bromide

methylaluminum sesquichloride

methylaluminum sesquichloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
Stage #1: methyl bromide With magnesium In tetrahydrofuran at 60℃; for 4h; Inert atmosphere;
Stage #2: methylaluminum sesquichloride In hexane at 40℃; for 6h; Inert atmosphere;
85%
(triphenylphosphine)trimethylaluminum

(triphenylphosphine)trimethylaluminum

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In neat (no solvent) metal complex decomposed at 120-130°C for 2-3 h;84%
aluminium(III) iodide

aluminium(III) iodide

methyl iodide
74-88-4

methyl iodide

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
Stage #1: methyl iodide With magnesium In diethyl ether at 15℃; for 1h; Inert atmosphere;
Stage #2: aluminium(III) iodide In pentane at 30℃; for 4h; Inert atmosphere;
81%
methylene chloride
74-87-3

methylene chloride

methylaluminum sesquichloride

methylaluminum sesquichloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
Stage #1: methylene chloride With magnesium at 80℃; for 6h; Inert atmosphere;
Stage #2: methylaluminum sesquichloride at 60℃; for 8h; Inert atmosphere;
81%
(CH2)5(P(C6H5)2Al(CH3)3)2

(CH2)5(P(C6H5)2Al(CH3)3)2

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In neat (no solvent) metal complex decomposed at 120-140°C for 2-3 h;80%
methyl bromide
74-83-9

methyl bromide

aluminum tri-bromide

aluminum tri-bromide

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
Stage #1: methyl bromide With magnesium In tetrahydrofuran at 40℃; for 3h; Inert atmosphere;
Stage #2: aluminum tri-bromide In hexane at 40℃; for 7h; Inert atmosphere;
79%
methyl aluminium sesquichloride

methyl aluminium sesquichloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
With sodium In mineral oil at 120 - 140℃; under 19.502 Torr; for 5.5h; Inert atmosphere;76.7%
triethylaluminum
97-93-8

triethylaluminum

aluminium
7429-90-5

aluminium

A

trimethylaluminum
75-24-1

trimethylaluminum

B

dimethyl aluminum iodide
2938-72-9

dimethyl aluminum iodide

Conditions
ConditionsYield
With iodine; methyl iodide In ethanol Sonication; N2, CH3I, I2 and Al introduced in a condenser with C2H5OH at -20°C, ultrasonic acceleration at room temp. for 2 h, Et3Al (ratio MeI/Et3Al = 3.00) dropped into soln. within 10 min, sonicated for 30 min; distilled (vac.);A 76%
B 11.2%
With iodine; methyl iodide In ethanol Sonication; N2, CH3I, I2 and Al introduced in a condenser with C2H5OH at -20°C, ultrasonic acceleration at room temp. for 2 h, Et3Al (ratio MeI/Et3Al = 6.00) dropped into soln. within 10 min, sonicated for 30 min; distilled (vac.);A 65%
B 15.7%
aluminum (III) chloride
7446-70-0, 7784-13-6

aluminum (III) chloride

methylene chloride
74-87-3

methylene chloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
Stage #1: methylene chloride With magnesium In tetrahydrofuran at 60℃; for 6h; Inert atmosphere;
Stage #2: aluminum (III) chloride In hexane at 50℃; for 11h; Inert atmosphere;
76%
2,2,7,7-tetramethyl-octa-3,5-diyne
6130-98-9

2,2,7,7-tetramethyl-octa-3,5-diyne

dimethylaluminum hydride
865-37-2

dimethylaluminum hydride

A

Al4H3(CH3)6((CH3)3CCCHCCH2C(CH3)3)

Al4H3(CH3)6((CH3)3CCCHCCH2C(CH3)3)

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In neat (no solvent) under Ar atm. excess Me2AlH and di(tert-butyl)butadiyne were stirred at 100°C for 1.5 h; react. mixt. was cooled to room temp., volatiles were removed in vacuo, residue was dissolved in n-pentane and cooled to -15°C;A 70%
B n/a
methylene chloride
74-87-3

methylene chloride

Reaxys ID: 23508781

Reaxys ID: 23508781

dimethylaluminum chloride
1184-58-3

dimethylaluminum chloride

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
Stage #1: dimethylaluminum chloride With pyridine; iodine In dodecane at 40℃; for 1.5h; Autoclave;
Stage #2: methylene chloride In dodecane at 130℃; for 24h; Temperature; Reagent/catalyst;
70%
tris(η2-tetramethylaluminato)yttrium(III)

tris(η2-tetramethylaluminato)yttrium(III)

[1,1':3',1''-terphenyl]-2'-carboxylic acid
5547-35-3

[1,1':3',1''-terphenyl]-2'-carboxylic acid

A

(Y((2,6-diphenylbenzoate)[(μ-Me)2AlMe2]2)2

(Y((2,6-diphenylbenzoate)[(μ-Me)2AlMe2]2)2

B

trimethylaluminum
75-24-1

trimethylaluminum

Conditions
ConditionsYield
In hexane; toluene byproducts: CH4; in a glovebox, Nd-contg. compd. (0.40 mmol) was dissolved in hexane, anda toluene suspn. of carboxylic acid (0.40 mmol) was slowly added; stirr ing at ambient temp. for 18 h; the solvent was removed in vac.; extn. in toluene; the complex was washed with hexane and dried for several hours; purifn. by crystn.; elem. anal.;A 64%
B n/a
1-chloro-4-trimethylsilyl but-3-yne
58435-00-0

1-chloro-4-trimethylsilyl but-3-yne

trimethylaluminum
75-24-1

trimethylaluminum

2-methyl-1-(trimethylsilyl)cyclobutene
86994-12-9

2-methyl-1-(trimethylsilyl)cyclobutene

Conditions
ConditionsYield
With zirconocene dichloride In dichloromethane at 25℃; for 24h;100%
With zirconocene dichloride In dichloromethane at 25℃; for 24h;95 % Chromat.
4-iodo-1-butynyltrimethylsilane
41423-29-4

4-iodo-1-butynyltrimethylsilane

trimethylaluminum
75-24-1

trimethylaluminum

2-methyl-1-(trimethylsilyl)cyclobutene
86994-12-9

2-methyl-1-(trimethylsilyl)cyclobutene

Conditions
ConditionsYield
With zirconocene dichloride In dichloromethane at 25℃; for 24h;100%
With zirconocene dichloride In dichloromethane at 25℃; for 24h;85%
trimethylaluminum
75-24-1

trimethylaluminum

(S)-2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-6-oxo-hexanoic acid methyl ester
156479-95-7

(S)-2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-6-oxo-hexanoic acid methyl ester

(S)-2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-6-hydroxy-heptanoic acid methyl ester

(S)-2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-6-hydroxy-heptanoic acid methyl ester

Conditions
ConditionsYield
In hexane; dichloromethane at 0℃;100%
trans-chrotonyl chloride
625-35-4, 3488-22-0, 10487-71-5

trans-chrotonyl chloride

trimethylaluminum
75-24-1

trimethylaluminum

trans-3-penten-2-one
3102-33-8

trans-3-penten-2-one

Conditions
ConditionsYield
With aluminium trichloride In dichloromethane for 2h; Ambient temperature;100%
With aluminium trichloride 1.) CH2Cl2, 1 h, 2.) CH2Cl2, room temperature, 2 h; other reagents: GaCl3, AlF3; Yield given. Multistep reaction;
5-hexyl-1-ol
928-90-5

5-hexyl-1-ol

trimethylaluminum
75-24-1

trimethylaluminum

5-methylhex-5-en-1-ol
5212-80-6

5-methylhex-5-en-1-ol

Conditions
ConditionsYield
With zirconocene dichloride In hexane; 1,2-dichloro-ethane at 20℃; for 22h; Addition;100%
trimethylaluminum
75-24-1

trimethylaluminum

(R)-1,4-Dioxa-spiro[4.5]decane-2-carboxylic acid (2S,3R)-2-(2-benzyloxy-ethyl)-tetrahydro-pyran-3-yl ester
286958-06-3

(R)-1,4-Dioxa-spiro[4.5]decane-2-carboxylic acid (2S,3R)-2-(2-benzyloxy-ethyl)-tetrahydro-pyran-3-yl ester

(R)-2-{1-[(2S,3R)-2-(2-Benzyloxy-ethyl)-tetrahydro-pyran-3-yloxy]-vinyl}-1,4-dioxa-spiro[4.5]decane
286958-07-4

(R)-2-{1-[(2S,3R)-2-(2-Benzyloxy-ethyl)-tetrahydro-pyran-3-yloxy]-vinyl}-1,4-dioxa-spiro[4.5]decane

Conditions
ConditionsYield
Stage #1: trimethylaluminum With bis(cyclopentadienyl)titanium dichloride In toluene at 23℃; for 72h; complex formation;
Stage #2: (R)-1,4-Dioxa-spiro[4.5]decane-2-carboxylic acid (2S,3R)-2-(2-benzyloxy-ethyl)-tetrahydro-pyran-3-yl ester In tetrahydrofuran; toluene at 0 - 23℃; olefination;
100%
trimethylaluminum
75-24-1

trimethylaluminum

benzaldehyde
100-52-7

benzaldehyde

(R)-1-phenylethanol
1517-69-7

(R)-1-phenylethanol

Conditions
ConditionsYield
With titanium(IV) isopropylate; (R,S)-2-OH-3,5-Cl2-C6H2-SO2-NH-CH(CH2Ph)-CH(Ph)OH In tetrahydrofuran at 0℃; for 12h;100%
In tetrahydrofuran; hexane at -20℃; for 3h; Product distribution / selectivity;60%
trimethylaluminum
75-24-1

trimethylaluminum

4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-D-glucono-1,5-lactone
498554-04-4

4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-D-glucono-1,5-lactone

(1R,3R,6R,9R,10S)-9,10-bis(tert-butyldimethylsilyloxy)-8-methylene-3-phenyl-2,4,7-trioxabicyclo[4.4.0]decane
498554-05-5

(1R,3R,6R,9R,10S)-9,10-bis(tert-butyldimethylsilyloxy)-8-methylene-3-phenyl-2,4,7-trioxabicyclo[4.4.0]decane

Conditions
ConditionsYield
Stage #1: trimethylaluminum With titanocene dichloride In toluene at 23℃; for 72h;
Stage #2: 4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-D-glucono-1,5-lactone In tetrahydrofuran; toluene at 0 - 24℃; Tebbe olefination;
100%
trimethylaluminum
75-24-1

trimethylaluminum

propargyl alcohol
107-19-7

propargyl alcohol

(1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxaldehyde
80434-59-9

(1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxaldehyde

(E)-1-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyl)-3-methyl-but-2-ene-1,4-diol

(E)-1-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyl)-3-methyl-but-2-ene-1,4-diol

Conditions
ConditionsYield
Stage #1: trimethylaluminum With bis(cyclopentadienyl)dihydrozirconium In dichloromethane for 0.166667h;
Stage #2: propargyl alcohol In dichloromethane at 20℃; for 12h;
Stage #3: (1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbaldehyde In tetrahydrofuran; dichloromethane at -78 - 20℃; for 12h;
100%
Stage #1: trimethylaluminum With zirconocene dichloride In dichloromethane at 20℃; for 0.166667h;
Stage #2: propargyl alcohol In dichloromethane at 0 - 20℃;
Stage #3: (1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbaldehyde In tetrahydrofuran; dichloromethane at -70 - 20℃;
1,8-dichloro-9-methylanthracene
17122-96-2

1,8-dichloro-9-methylanthracene

trimethylaluminum
75-24-1

trimethylaluminum

1,8,9-trimethylanthracene
63335-10-4

1,8,9-trimethylanthracene

Conditions
ConditionsYield
With 1,3-bis[(diphenylphosphino)propane]dichloronickel(II) In 1,2-dimethoxyethane; hexane for 7h; Heating;100%
3,3-diphenyloxirane-2-carboxylic acid methyl ester
76527-25-8

3,3-diphenyloxirane-2-carboxylic acid methyl ester

trimethylaluminum
75-24-1

trimethylaluminum

(+/-)-methyl 2-hydroxy-3,3-diphenylbutanoate
178306-50-8

(+/-)-methyl 2-hydroxy-3,3-diphenylbutanoate

Conditions
ConditionsYield
In cyclohexane; toluene at 10 - 15℃; for 0.5h; Product distribution / selectivity;100%
In cyclohexane at 10℃; Product distribution / selectivity;96%
In n-heptane; toluene at -10℃; for 0.5h; Product distribution / selectivity;82%
In toluene at -10 - 10℃; Product distribution / selectivity;82%
trimethylaluminum
75-24-1

trimethylaluminum

polymethylaluminoxane

polymethylaluminoxane

Conditions
ConditionsYield
With benzoic acid In toluene at 26 - 80℃; for 9.5h;100%
1,4,7,10-tetrathiacyclododecane
25423-56-7

1,4,7,10-tetrathiacyclododecane

trimethylaluminum
75-24-1

trimethylaluminum

trimethylaluminum-thiacrown ether {12}aneS4
112440-15-0

trimethylaluminum-thiacrown ether {12}aneS4

Conditions
ConditionsYield
In toluene addn. of Me3Al to {12}aneS4 in abs. toluene , heated at 60°C for several h; solvent reduced in vacuo, cooling;100%
bis(cyclopentadienyl)titanium dichloride
1271-19-8

bis(cyclopentadienyl)titanium dichloride

trimethylaluminum
75-24-1

trimethylaluminum

bis(cyclopentadienyl)methyltitanium(IV) chloride
1278-83-7

bis(cyclopentadienyl)methyltitanium(IV) chloride

Conditions
ConditionsYield
With tetrahydrofuran In benzene-d6; toluene N2 or Ar-atmosphere; stirring (22°C, 1 h), THF addn.; detd. by NMR spectroscopy;100%
trimethylaluminum
75-24-1

trimethylaluminum

magnesium bis(N,N-diisopropylamide)

magnesium bis(N,N-diisopropylamide)

A

[(CH3)2Al(N(C3H7)2)2Al(CH3)2]

[(CH3)2Al(N(C3H7)2)2Al(CH3)2]

B

{(CH3)2Al{N(C3H7)2}2Mg(CH3)}4

{(CH3)2Al{N(C3H7)2}2Mg(CH3)}4

Conditions
ConditionsYield
In diethyl ether; toluene absence of air and moisture; dropwise addn. of AlMe3 in toluene to Mg(N(C3H7)2)2 in Et2O (molar ratio = 1 : 1, room temp., stirring); after 12h removal of solvent (vac.), recrystn. (hexane), sublimation (60°C); elem. anal.;A <5
B 100%
trimethylaluminum
75-24-1

trimethylaluminum

triphenylplumbyl hydroxide
894-08-6

triphenylplumbyl hydroxide

A

methylaluminoxane

methylaluminoxane

B

(triphenylplumbyl)methane
3124-28-5

(triphenylplumbyl)methane

Conditions
ConditionsYield
byproducts: CH4; not isolated, detected by NMR;A n/a
B 100%
trimethylaluminum
75-24-1

trimethylaluminum

triphenyltin(IV) hydroxide
76-87-9

triphenyltin(IV) hydroxide

A

methylaluminoxane

methylaluminoxane

B

triphenyl methyl tin
1089-59-4

triphenyl methyl tin

Conditions
ConditionsYield
byproducts: CH4; not isolated, detected by NMR;A n/a
B 100%
(CH3)2AlNHCH2CH2N(CH3)2
102990-34-1

(CH3)2AlNHCH2CH2N(CH3)2

trimethylaluminum
75-24-1

trimethylaluminum

(CH3)2Al(NH(Al(CH3)3)CH2CH2N(CH3)2)

(CH3)2Al(NH(Al(CH3)3)CH2CH2N(CH3)2)

Conditions
ConditionsYield
In dichloromethane Ar-atmosphere; addn. of Al-compd. (0°C); gradual warming to room temp. (2 h); evapn.;100%
(CH3)3SiNC(C6H5)CH2C(C6H5)NSi(CH3)3
912272-65-2

(CH3)3SiNC(C6H5)CH2C(C6H5)NSi(CH3)3

trimethylaluminum
75-24-1

trimethylaluminum

[AlMe2(CH(C(Ph)NSiMe3)2)]
226717-58-4

[AlMe2(CH(C(Ph)NSiMe3)2)]

Conditions
ConditionsYield
In hexane; pentane addn. of Me3Al in hexane to ligand in pentane at -78°C; accordingto P. B. Hitchcock, M. F. Lappert and D.-S Liu, J. Chem. Soc., Chem. Co mmun., 1994, 1699; elem. anal.;100%
tris(pentafluorophenyl)borate
1109-15-5

tris(pentafluorophenyl)borate

trimethylaluminum
75-24-1

trimethylaluminum

toluene
108-88-3

toluene

tris(pentafluorophenyl)aluminum*(toluene)0.5

tris(pentafluorophenyl)aluminum*(toluene)0.5

Conditions
ConditionsYield
In hexane100%
In hexane; toluene B(C6F5)3 and AlMe3 in 1:3 toluene/hexanes mixt.;99%
In hexane; toluene (inert atm.); reaction of borane deriv. with trimethylaluminium in hexane/toluene (3:1);99%
2,3,4,5,6-pentafluorophenol
771-61-9

2,3,4,5,6-pentafluorophenol

trimethylaluminum
75-24-1

trimethylaluminum

Al(OC6F5)3

Al(OC6F5)3

Conditions
ConditionsYield
In hexane (inert atmosphere); -30°C slowly to room temp., stirring (2 h); evapn. to dryness, washing (hexane);100%
trimethylaluminum
75-24-1

trimethylaluminum

tetraethyldistibine
4669-92-5

tetraethyldistibine

[Et4Sb2][AlMe3]2

[Et4Sb2][AlMe3]2

Conditions
ConditionsYield
In neat (no solvent) under N2 atm. react. Me3Al and Et4Sb2; elem. anal.;100%
trimethylaluminum
75-24-1

trimethylaluminum

N,N',N'-Trimethyl-hexamethylcyclotristannazan
1080-40-6

N,N',N'-Trimethyl-hexamethylcyclotristannazan

[(CH3)2AlN(Sn(CH3)3)(CH3)]2

[(CH3)2AlN(Sn(CH3)3)(CH3)]2

Conditions
ConditionsYield
In toluene molar ratio 3:1;100%
trimethylaluminum
75-24-1

trimethylaluminum

tris(diethylamino)difluorophosphorane
32318-29-9

tris(diethylamino)difluorophosphorane

[FP(N(C2H5)2)3](1+)*[(CH3)3AlF](1-)=[FP(N(C2H5)2)3][(CH3)3AlF]
222190-83-2

[FP(N(C2H5)2)3](1+)*[(CH3)3AlF](1-)=[FP(N(C2H5)2)3][(CH3)3AlF]

Conditions
ConditionsYield
In tetrahydrofuran Ar atm.; equimolar amts., stirring (20°C, 24 h); evapn. (vac.); elem. anal.;100%
trimethylaluminum
75-24-1

trimethylaluminum

N.N'.N''-Triethyl-hexamethyl-hexahydro-symm.-triazatristannin
1778-12-7

N.N'.N''-Triethyl-hexamethyl-hexahydro-symm.-triazatristannin

[(CH3)2AlN(Sn(CH3)3)(CH2CH3)]2

[(CH3)2AlN(Sn(CH3)3)(CH2CH3)]2

Conditions
ConditionsYield
In toluene molar ratio 3:1;100%
[(CH3)2SnN(CH(CH3)2)]3
234443-32-4

[(CH3)2SnN(CH(CH3)2)]3

trimethylaluminum
75-24-1

trimethylaluminum

[(CH3)2AlN(Sn(CH3)3)(CH(CH3)2)]2

[(CH3)2AlN(Sn(CH3)3)(CH(CH3)2)]2

Conditions
ConditionsYield
In toluene molar ratio 3:1;100%
In toluene dry Ar atm.; 3 equiv. of AlMe3, cooling (-15°C), heating (room temp., stirring), refluxing (1,5 h, 70-80°C); concn., standing (5 to -5 degree.C, several days), washing (toluene), drying (vac.); elem. anal.;54%
[(CH3)2SnN(CH2CH2CH3)]3
234443-31-3

[(CH3)2SnN(CH2CH2CH3)]3

trimethylaluminum
75-24-1

trimethylaluminum

[(CH3)2AlN(Sn(CH3)3)(CH2CH2CH3)]2

[(CH3)2AlN(Sn(CH3)3)(CH2CH2CH3)]2

Conditions
ConditionsYield
In toluene molar ratio 3:1;100%
In toluene dry Ar atm.; 3 equiv. of AlMe3, cooling (-15°C), heating (room temp., stirring), refluxing (1,5 h, 70-80°C); concn., standing (5 to -5 degree.C, several days), washing (toluene), drying (vac.); elem. anal.;57%
[(CH3)2SnN(CH2CH(CH3)2)]3
234443-33-5

[(CH3)2SnN(CH2CH(CH3)2)]3

trimethylaluminum
75-24-1

trimethylaluminum

[(CH3)2AlN(Sn(CH3)3)(CH2CH(CH3)2)]2

[(CH3)2AlN(Sn(CH3)3)(CH2CH(CH3)2)]2

Conditions
ConditionsYield
In toluene molar ratio 3:1;100%
In toluene dry Ar atm.; 3 equiv. of AlMe3, cooling (-15°C), heating (room temp., stirring), refluxing (1,5 h, 70-80°C); concn., standing (5 to -5 degree.C, several days), washing (toluene), drying (vac.); elem. anal.;58%
[(CH3)2SnNCH(CH3)(CH2CH3)]3

[(CH3)2SnNCH(CH3)(CH2CH3)]3

trimethylaluminum
75-24-1

trimethylaluminum

[(CH3)2AlN(Sn(CH3)3)((CH3)CH(CH2CH3))]2

[(CH3)2AlN(Sn(CH3)3)((CH3)CH(CH2CH3))]2

Conditions
ConditionsYield
In toluene molar ratio 3:1;100%
tris(trimethylsilyl)bismuthane
81183-20-2

tris(trimethylsilyl)bismuthane

trimethylaluminum
75-24-1

trimethylaluminum

(CH3)3AlBi(Si(CH3)3)3

(CH3)3AlBi(Si(CH3)3)3

Conditions
ConditionsYield
In neat (no solvent) substances mixted in glove box, N2; detd. by elem. anal., NMR;100%
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