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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

N,N-Dimethylallylamine Manufacturer/High quality/Best price/In stock

Cas:2155-94-4

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

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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

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:5 Kiloliter

FOB Price: $1.2 / 5.0

Type:Manufacturers

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Henan Tianfu Chemical Co., Ltd.

TIANFUCHEM--2155-94-4--N,N-Dimethylallylamine factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable business

TIANFUCHEM--2155-94-4--N,N-Dimethylallylamine factory price

Cas:2155-94-4

Min.Order:1 Metric Ton

FOB Price: $2000.0

Type:Lab/Research institutions

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Hebei Nengqian Chemical Import and Export Co., LTD

Our advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:1 Kilogram

FOB Price: $9.0 / 99.0

Type:Trading Company

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Zhuozhou Wenxi import and Export Co., Ltd

WITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et

Competitve Price in stock CAS 2155-94-4 with best price

Cas:2155-94-4

Min.Order:10 Gram

FOB Price: $146.0 / 176.0

Type:Trading Company

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Henan Sinotech Import&Export Corporation

Name: N, N-Dimethylallylamine( DMAA) CAS:2155-94-4 MF: C5H12N Purity: 99% Use:Intermediate for chemical synthesis can be used as pesticides; cationic quaternary ammonium salt monomer, pharmaceutical intermediates Appearance: Colorless Liquid Sto

N, N-Dimethylallylamine

Cas:2155-94-4

Min.Order:1 Kilogram

FOB Price: $1.0

Type:Other

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Shanghai Upbio Tech Co.,Ltd

1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized

2-Propen-1-amine,N,N-dimethyl- 2155-94-4

Cas:2155-94-4

Min.Order:1 Kilogram

Negotiable

Type:Lab/Research institutions

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Qingdao Beluga Import and Export Co., LTD

N,N-Dimethylallylamine CAS:2155-94-4 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic int

N,N-Dimethylallylamine CAS:2155-94-4

Cas:2155-94-4

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

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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.:2155-94-4

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Changchun Artel lmport and Export trade company

Price, service, company and transport advantage : 1. best service, high quality and reasonable price 2. it's customers' right to choose the package (ems, dhl, fedex, ups); 3. it's customers' r

Beat price/N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:10 Gram

Negotiable

Type:Trading Company

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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

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Hangzhou Fonlynn Health Technology Co., Ltd.

Packing: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once Transportation:Express/Sea/Air Port:Ningbo/Shanghai/Qingd

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Trading Company

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Chemlyte Solutions

Chemlyte Solutions believe that customers and suppliers deserve much more than what traditional distributors can offer. To grow in today s fast-paced and increasingly competitive market it is essential to be able to quickly adapt to market forces eff

Featured products N,N-dimethylallylamide

Cas:2155-94-4

Min.Order:100 Gram

Negotiable

Type:Other

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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

high quality 1D-Biotin powder

Cas:2155-94-4

Min.Order:10 Gram

FOB Price: $100.0

Type:Lab/Research institutions

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HANGZHOU YUNUO CHEMICAL CO.,LTD

Superior quality moderate price & quick delivery Appearance:colourless to faintly yellow liquid 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. Applicat

N,N-Dimethylallylamine;Allyldimethylamine

Cas:2155-94-4

Min.Order:1 Kilogram

Negotiable

Type:Trading Company

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Zibo Dorne chemical technology co. LTD

Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,

High purity N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:1 Kilogram

Negotiable

Type:Lab/Research institutions

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Shanghai Minstar Chemical Co., Ltd

N,N-Dimethylallylamine Basic information Product Name: N,N-Dimethylallylamine Synonyms: 2-Propen-1-amine, N,N-dimethyl-;N,N-DiMethylallylaMine, 98% 5GR;N-Allyldimethylamine 1-Dimethylamino-2-propene;N,N-DIMETHYLALLYLAMINE FOR SYNTHESIS;Allylam

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

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KAISA GROUP INC

1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer

Beat price/N,N-Dimethylallylamine CAS NO.2155-94-4

Cas:2155-94-4

Min.Order:1 Metric Ton

FOB Price: $7.0 / 8.0

Type:Trading Company

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Hangzhou Zhongqi chem Co.,Ltd.

Located in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service an

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:1 Gram

Negotiable

Type:Other

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Hunan chemfish Pharmaceutical co.,Ltd

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

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Manufacturers

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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

N,N-Dimethylallylamine;Allyldimethylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Other

inquiry

GIHI CHEMICALS CO.,LIMITED

high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Henan Allgreen Chemical Co.,Ltd

high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea

N,N-DiMethylallylaMine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Manufacturers

inquiry

SHANGHAI SYSTEAM BIOCHEM CO., LTD

N,N-Dimethylallylamine (We a a few suppliers that can offer custom synthesis service of this product) We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are commit

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0 Metric Ton

Negotiable

Type:Lab/Research institutions

inquiry

Wuhan Circle Star Chem-medical Technology co.,Ltd.

1,we produce and sell good chemicals around the world.2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%.3,our staff consists of highly qualified in

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Lab/Research institutions

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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

N,N-DiMethylallylaMine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Hangzhou Fandachem Co.,Ltd

N,N-DimethylallylamineAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Other

inquiry

Hangzhou Sartort Biopharma Co., Ltd

Best quality with low priceAppearance:colourless to faintly yellow liquid Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Shanghai

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Hubei Jiutian Bio-medical Technology Co., Ltd

Trimeric sodium phosphate detergent auxiliary agent is a kind of excellent properties, is one of the biggest component of detergent consumption during the production, it has four aspects: 1, chelation of heavy metal ions, heavy metal ions in the wate

N,N-Dimethylallylamine

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Shanghai Chinqesen Biotechnology Co., Ltd.

Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen

2155-94-4

Cas:2155-94-4

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

N,N-Dimethylpropargylamin
7223-38-3

N,N-Dimethylpropargylamin

A

N,N-dimethylaminopropane
926-63-6

N,N-dimethylaminopropane

B

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics;A n/a
B 100%
N,N-Dimethylpropargylamin
7223-38-3

N,N-Dimethylpropargylamin

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760.051 Torr;100%
With piperazine; hydrogen In ethanol at 80℃; under 4500.45 Torr; for 24h;99%
With piperazine; hydrogen In ethanol at 100℃; under 4500.45 Torr; for 24h; Green chemistry;
With hydrogen In ethanol at 100℃; under 4500.45 Torr; for 24h; chemoselective reaction;96 %Chromat.
Allyl-dimethyl-(1-naphthalen-1-ylethynyl-but-3-enyl)-ammonium; bromide

Allyl-dimethyl-(1-naphthalen-1-ylethynyl-but-3-enyl)-ammonium; bromide

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

2,2-dimethyl-1-allyl-3a,4-dihydronaphtisoindolenium bromide

2,2-dimethyl-1-allyl-3a,4-dihydronaphtisoindolenium bromide

Conditions
ConditionsYield
With potassium hydroxide In water at 90 - 92℃; for 1.5h;A 8%
B 71%
Allyl-dimethylcarbamoylmethyl-dimethyl-ammonium; bromide
102990-43-2

Allyl-dimethylcarbamoylmethyl-dimethyl-ammonium; bromide

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

2-(dimethylamino)-N,N-dimethylacetamide
13574-14-6

2-(dimethylamino)-N,N-dimethylacetamide

C

2-Dimethylamino-pent-4-enoic acid dimethylamide
102990-49-8

2-Dimethylamino-pent-4-enoic acid dimethylamide

Conditions
ConditionsYield
With potassium hydroxide In benzene at 65 - 70℃; for 1h; metallic sodium in DMSO was also used instead of potassium hydroxide;A n/a
B n/a
C 70%
Allyl-(1-methoxycarbonyl-ethyl)-dimethyl-ammonium; bromide
80070-14-0

Allyl-(1-methoxycarbonyl-ethyl)-dimethyl-ammonium; bromide

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

2-Dimethylamino-2-methyl-pent-4-enoic acid methyl ester
80070-19-5

2-Dimethylamino-2-methyl-pent-4-enoic acid methyl ester

C

acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

Conditions
ConditionsYield
With sodium methylate In diethyl ether at 30 - 35℃; Yield given;A n/a
B 69%
C n/a
With sodium methylate In diethyl ether at 30 - 35℃; Yields of byproduct given;A n/a
B 69%
C n/a
dimethyl amine
124-40-3

dimethyl amine

allyl bromide
106-95-6

allyl bromide

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
In water 1) 30 min, 2) reflux, 30 min.;62.5%
In water Ambient temperature;51%
In benzene36%
formaldehyd
50-00-0

formaldehyd

1-amino-2-propene
107-11-9

1-amino-2-propene

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With formic acid for 8h; Heating;58%
formic acid
64-18-6

formic acid

1-amino-2-propene
107-11-9

1-amino-2-propene

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With formaldehyd In water at 100℃; for 12h;46%
sodium methylate
124-41-4

sodium methylate

allyl bromide
106-95-6

allyl bromide

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
copper(l) chloride In water30%
{C5H5FeC5H4CH2N(CH3)2CH2CHCH2}(1+)*Br(1-)={C5H5FeC5H4CH2N(CH3)2CH2CHCH2}Br

{C5H5FeC5H4CH2N(CH3)2CH2CHCH2}(1+)*Br(1-)={C5H5FeC5H4CH2N(CH3)2CH2CHCH2}Br

A

methyl ferrocene

methyl ferrocene

B

N,N-dimethylaminomethylferrocene
1271-86-9

N,N-dimethylaminomethylferrocene

C

propene
187737-37-7

propene

D

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With sodium In ammoniaA 30%
B 26%
C n/a
D n/a
With Na In ammonia NH3 (liquid);A 30%
B 26%
C n/a
D n/a
formic acid
64-18-6

formic acid

allyl-trimethyl-ammonium; hydroxide
503-34-4

allyl-trimethyl-ammonium; hydroxide

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

Methyl formate
107-31-3

Methyl formate

C

3-formyloxy-propene
1838-59-1

3-formyloxy-propene

D

trimethylamine
75-50-3

trimethylamine

Conditions
ConditionsYield
at 190 - 200℃;
allyl trimethylammonium bromide
3004-51-1

allyl trimethylammonium bromide

ethanolamine
141-43-5

ethanolamine

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

trimethylamine
75-50-3

trimethylamine

Conditions
ConditionsYield
at 154℃; Rate constant;
allyl iodid
556-56-9

allyl iodid

dimethyl amine
124-40-3

dimethyl amine

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With ethanol at 150℃;
dimethyl amine
124-40-3

dimethyl amine

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With sodium hydroxide
Stage #1: dimethyl amine; 3-chloroprop-1-ene In water at 20 - 30℃; Autoclave;
Stage #2: With sodium hydroxide In water for 0.333333h; pH=11 - 13; pH-value; Autoclave;
N-methyl-N-allylamine
627-37-2

N-methyl-N-allylamine

methyl bromide
74-83-9

methyl bromide

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

N-benzyl-N,N-dimethylprop-2-en-1-ylammonium bromide
22100-10-3

N-benzyl-N,N-dimethylprop-2-en-1-ylammonium bromide

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With sodium hydroxide; thiophenol
Allyl-dimethyl-<4-chlor-butin-(2)-yl>-ammonium

Allyl-dimethyl-<4-chlor-butin-(2)-yl>-ammonium

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With potassium hydroxide
3-(dimethylamino)-1-propyl acetate
4339-94-0

3-(dimethylamino)-1-propyl acetate

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

acetic acid methyl ester
79-20-9

acetic acid methyl ester

C

N,N'-dimethyl-1-propenylamine
6163-56-0

N,N'-dimethyl-1-propenylamine

D

acetic acid
64-19-7

acetic acid

E

dimethyl amine
124-40-3

dimethyl amine

F

prop-1-yne
74-99-7

prop-1-yne

Conditions
ConditionsYield
at 347.1℃; Mechanism; Kinetics; other temperatures, various pressures, effect of propene inhibitors; Ea, log A;
Allyl-but-2-inyl-dimethyl-ammonium
105380-01-6

Allyl-but-2-inyl-dimethyl-ammonium

A

3-buten-1-yne
689-97-4

3-buten-1-yne

B

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With potassium hydroxide; tert-butylamine at 50℃; Yield given;
trimethylene-bis-trimethylammonium hydroxide

trimethylene-bis-trimethylammonium hydroxide

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
bei der Destillation;
1,1,5,5-tetramethyl-octahydro-[1,5]diazocinediium; dichloride

1,1,5,5-tetramethyl-octahydro-[1,5]diazocinediium; dichloride

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

dimethylamine,tetramethyl-trimethylenediamine,diisopropenyl ether

dimethylamine,tetramethyl-trimethylenediamine,diisopropenyl ether

Conditions
ConditionsYield
With potassium hydroxide durch Destillation;
1,1,5,5-tetramethyl-octahydro-[1,5]diazocinediium; dichloride

1,1,5,5-tetramethyl-octahydro-[1,5]diazocinediium; dichloride

KOH-solution

KOH-solution

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

bisisopropenyl ether
4188-73-2

bisisopropenyl ether

C

dimethyl amine
124-40-3

dimethyl amine

D

N.N.N'.N'-tetramethyl-trimethylenediamine

N.N.N'.N'-tetramethyl-trimethylenediamine

hexa-N-methyl-N,N'-propanediyl-di-ammonium; dihydroxyide
105850-86-0

hexa-N-methyl-N,N'-propanediyl-di-ammonium; dihydroxyide

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

4-methylpent-4-en-2-one
3744-02-3

4-methylpent-4-en-2-one

C

trimethylamine
75-50-3

trimethylamine

D

N.N.N'.N'-tetramethyl-trimethylenediamine

N.N.N'.N'-tetramethyl-trimethylenediamine

Conditions
ConditionsYield
bei der Destillation;
3-dimethylamino-2-methyl-N-isopropylpropanamide
282097-60-3

3-dimethylamino-2-methyl-N-isopropylpropanamide

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

N-isopropylmethacrylamide
13749-61-6

N-isopropylmethacrylamide

Conditions
ConditionsYield
In water
hexadecyl allyl carbonate
959078-65-0

hexadecyl allyl carbonate

diethylamine
109-89-7

diethylamine

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

1-Hexadecanol
36653-82-4

1-Hexadecanol

Conditions
ConditionsYield
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere;
allyl 1-decyl carbonate
40940-42-9

allyl 1-decyl carbonate

diethylamine
109-89-7

diethylamine

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

1-Decanol
112-30-1

1-Decanol

Conditions
ConditionsYield
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere;
diethylamine
109-89-7

diethylamine

allyl butyl carbonate
16308-66-0

allyl butyl carbonate

A

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

B

butan-1-ol
71-36-3

butan-1-ol

Conditions
ConditionsYield
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere;
diethylamine
109-89-7

diethylamine

allyl octyl carbonate

allyl octyl carbonate

A

octanol
111-87-5

octanol

B

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere;
diethylamine
109-89-7

diethylamine

allyl undecyl carbonate

allyl undecyl carbonate

A

undecyl alcohol
112-42-5

undecyl alcohol

B

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Conditions
ConditionsYield
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere;
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

carbon monoxide
201230-82-2

carbon monoxide

phenylhydrazine
100-63-0

phenylhydrazine

dimethyl-[4-(phenyl-hydrazono)-butyl]-amine

dimethyl-[4-(phenyl-hydrazono)-butyl]-amine

Conditions
ConditionsYield
With hydrogen; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; Rh(acac)2(CO)2 In tetrahydrofuran at 70℃; under 15001.2 Torr; for 68h;100%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

(E)-1-N,N-dimethylamino-1-propene
13222-51-0

(E)-1-N,N-dimethylamino-1-propene

Conditions
ConditionsYield
With hydridocarbonylbis(triphenylphosphine)rhodium(I) In benzene-d6 at 60℃; for 2h; Inert atmosphere;99%
+ In tetrahydrofuran at 17℃; for 23h; Yield given;
With trans-bisdinitrogenbis(1,2-diphenylphosphinoethane)molybdenum(0) In toluene for 2h; Heating;100 % Chromat.
carbonylhydridetris(triphenylphosphine)rhodium(I) In benzene-d6 at 60℃; for 2h;100 % Spectr.
With [(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]-(η4-1,5-cyclooctadiene)rhodium(I) perchlorate In tetrahydrofuran at 40℃; for 23h; Inert atmosphere;n/a
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

C32H79ClSi7

C32H79ClSi7

C52H123ClN4Si7

C52H123ClN4Si7

Conditions
ConditionsYield
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In tetrahydrofuran at 60℃; Inert atmosphere; Sealed tube;99%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Triethoxysilane
998-30-1

Triethoxysilane

N,N-dimethyl-3-(triethoxysilyl)-1-propylamine
43108-00-5

N,N-dimethyl-3-(triethoxysilyl)-1-propylamine

Conditions
ConditionsYield
With platinum-containing olefin organic polymer catalyst at 20℃; for 24h;98%
With (TFAPDI)Co(2-ethylhexanoate)2 In neat (no solvent) at 23℃; for 1h;74%
dicobalt octacarbonyl
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 80℃; for 20h; Schlenk technique; Inert atmosphere; regioselective reaction;94.8 %Spectr.
With C28H34CoN3O4(1+)*C5H7O2(1-) In tetrahydrofuran at 50℃; for 6h; Sealed tube;
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

(3aS,6R,7aR)-1-(bromoacetyl)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide
185748-26-9

(3aS,6R,7aR)-1-(bromoacetyl)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide

N-[2-(allyldimethylammonium)acetyl]-(1S,2R)-bornane-10,2-sultam

N-[2-(allyldimethylammonium)acetyl]-(1S,2R)-bornane-10,2-sultam

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 6h;98%
borane methyl sulfide complex

borane methyl sulfide complex

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

N,N-dimethyl allylamine-borane
23904-26-9

N,N-dimethyl allylamine-borane

Conditions
ConditionsYield
In diethyl ether (inert atm.); stirring (1 h, 0°C); MeOH addn., stirring (30 min, room temp.), solvent removal (vac.), trituration (petroleum ether), evpn. (vac.);98%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

diphenylsilane
775-12-2

diphenylsilane

N,N-dimethyl(diphenylsilyl)propan-1-amine

N,N-dimethyl(diphenylsilyl)propan-1-amine

Conditions
ConditionsYield
With C25H30N2NiO In acetonitrile at 25℃; for 1h;98%
With C25H31N2NiO In acetonitrile at 20℃; for 1h;98%
With N-(1-[2,2′-bipyridin-6-yl]ethylidene)-2,4,6-trimethylbenzenamine iron(II) bromide; sodium triethylborohydride In toluene at 20℃; for 24h; Catalytic behavior; Reagent/catalyst; Schlenk technique; Inert atmosphere;94%
dimethylphosphane
676-59-5

dimethylphosphane

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

A

3-(N,N-dimethylamino)-1-(dimethylphosphino)propane
50518-38-2

3-(N,N-dimethylamino)-1-(dimethylphosphino)propane

B

1,3-bis(dimethylphosphino)propane
39564-18-6

1,3-bis(dimethylphosphino)propane

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In diethyl ether at -20℃; for 24h; Product distribution; Mechanism; Irradiation; reactions under var. conditions;A 97%
B n/a
With 2,2'-azobis(isobutyronitrile) In diethyl ether at -20℃; for 24h; Irradiation;A 97%
B n/a
2-chloro-4,6-dimethoxy-1 ,3,5-triazine
3140-73-6

2-chloro-4,6-dimethoxy-1 ,3,5-triazine

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

2-(dimethylamino)-4,6-dimethoxy-1,3,5-triazine
13704-45-5

2-(dimethylamino)-4,6-dimethoxy-1,3,5-triazine

Conditions
ConditionsYield
In toluene Reflux;97%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

methyl iodide
74-88-4

methyl iodide

N,N,N-trimethylallylammonium iodide
13448-30-1

N,N,N-trimethylallylammonium iodide

Conditions
ConditionsYield
In diethyl ether at 20℃; for 3h; Inert atmosphere;97%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
25015-63-8

4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

C11H24BNO2
1437319-65-7

C11H24BNO2

Conditions
ConditionsYield
With C28H30CoNP In benzene-d6 at 20℃; for 0.5h; Inert atmosphere;97%
With [(2,6-(2,4,6-Me3-C6H2-NdCMe)2C5H3N)Fe(N2)]2(μ2-N2) In neat (no solvent) at 25℃; Reagent/catalyst; Inert atmosphere;
With (MesPDI)CoMe In neat (no solvent) at 23℃; for 0.25h; Schlenk technique; Inert atmosphere; Glovebox;
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

dimethyldiallylammonium chloride
7398-69-8

dimethyldiallylammonium chloride

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-2-propen-1-amine; 3-chloroprop-1-ene at 30 - 55℃; for 4.5h;
Stage #2: With sodium hydroxide pH=11; Temperature; pH-value;
97%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

methyl trifluoromethanesulfonate
333-27-7

methyl trifluoromethanesulfonate

N,N,N-trimethylprop-2-en-1-ammonium triflate

N,N,N-trimethylprop-2-en-1-ammonium triflate

Conditions
ConditionsYield
In diethyl ether at 0 - 20℃; for 2.25h; Schlenk technique; Inert atmosphere;97%
diazoacetic acid ethyl ester
623-73-4

diazoacetic acid ethyl ester

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

2-(N,N-dimethylamino)-4-pentenoic acid ethyl ester
66917-63-3

2-(N,N-dimethylamino)-4-pentenoic acid ethyl ester

Conditions
ConditionsYield
With 5,10,15,20-tetrakis(pentafluorophenyl)-21H,23H-porphyrin iron(III) chloride In dichloromethane at 20℃; for 0.0166667h;96%
carbonyl(5,10,15,20-tetraphenylporphyrinato)ruthenium(II) In toluene at 50℃; for 5h;87%
hexarhodium hexadecacarbonyl at 60℃;82%
With copper acetylacetonate In benzene at 60℃; for 22h; Inert atmosphere;35%
carbonyl(5,10,15,20-tetraphenylporphyrinato)ruthenium(II) In dichloromethane at 20℃; for 24h;100 % Chromat.
tetraallyltitanate
873410-49-2

tetraallyltitanate

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

methylphenylsilane
766-08-5

methylphenylsilane

{(CH3)2N(CH2)3Si(C6H5)(CH3)OTi(OC3H5)2O(CH2)3}2Si(CH3)C6H5
142414-22-0

{(CH3)2N(CH2)3Si(C6H5)(CH3)OTi(OC3H5)2O(CH2)3}2Si(CH3)C6H5

Conditions
ConditionsYield
dihydrogen hexachloroplatinate byproducts: propene; to a mixt. of titanate and silane (molar ratio 1:4) catalyst was added and heated to 100°C for 2.5 h; unreacted silane was removed at 50-80 °C and 1-2 Torr within 4 h; then titanosiloxane was reacted with excess amine at 50°C, 4 h;; unreacted amine was removed by heating in vac.; elem. anal.;;96%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

Conditions
ConditionsYield
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine In toluene Reflux;96%
H2SiEt2
542-91-6

H2SiEt2

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

C9H23NSi

C9H23NSi

Conditions
ConditionsYield
With C25H30N2NiO In acetonitrile at 25℃; for 1h;96%
With C25H31N2NiO In acetonitrile at 20℃; for 0.5h;96%
trimethoxysilane
2487-90-3

trimethoxysilane

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

A

<3-(dimethylamino)propyl>trimethoxysilane
2530-86-1

<3-(dimethylamino)propyl>trimethoxysilane

B

2-dimethylaminopropyltrimethoxysilane

2-dimethylaminopropyltrimethoxysilane

Conditions
ConditionsYield
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex; ammonium bicarbonate In toluene at 55℃; for 8h; Reagent/catalyst;A 95.5%
B 6.7%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

[N-(p-tolylsulfonyl)imino]phenyliodinane
55962-05-5

[N-(p-tolylsulfonyl)imino]phenyliodinane

2-allyl-2,2-dimethyl-1-tosylhydrazin-2-ium-1-ide

2-allyl-2,2-dimethyl-1-tosylhydrazin-2-ium-1-ide

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-2-propen-1-amine With 2C15H31BBr3N6(1-)*2Ag(1+) In dichloromethane for 0.0833333h; Inert atmosphere; Glovebox;
Stage #2: [N-(p-tolylsulfonyl)imino]phenyliodinane In dichloromethane at 50℃; for 16h; Inert atmosphere; Glovebox; chemoselective reaction;
95%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

1-diazo-2-heptadecanone
51865-45-3

1-diazo-2-heptadecanone

4-dimethylamino-1-eicosen-5-one

4-dimethylamino-1-eicosen-5-one

Conditions
ConditionsYield
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h;94%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

hexakis((4-dimethylsilyl)phenoxy)cyclotriphosphazene

hexakis((4-dimethylsilyl)phenoxy)cyclotriphosphazene

C78H132N9O6P3Si6

C78H132N9O6P3Si6

Conditions
ConditionsYield
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In toluene at 90℃; regioselective reaction;94%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

1-diazopentan-2-one
39910-26-4

1-diazopentan-2-one

5-dimethylamino-7-octen-4-one

5-dimethylamino-7-octen-4-one

Conditions
ConditionsYield
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h;93%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

1-diazo-2-tridecanone
57393-50-7

1-diazo-2-tridecanone

4-dimethylamino-1-hexadecen-5-one

4-dimethylamino-1-hexadecen-5-one

Conditions
ConditionsYield
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h;93%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

2,2-bis(4-dimethylsilylphenoxy)-4,4,6,6-bis[spiro(2’,2’’-dioxy-1’,1’’-biphenyl)]cyclotriphosphazene

2,2-bis(4-dimethylsilylphenoxy)-4,4,6,6-bis[spiro(2’,2’’-dioxy-1’,1’’-biphenyl)]cyclotriphosphazene

C50H60N5O6P3Si2

C50H60N5O6P3Si2

Conditions
ConditionsYield
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In toluene at 90℃; regioselective reaction;93%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

Triethoxysilane
998-30-1

Triethoxysilane

A

N,N-dimethyl-3-(triethoxysilyl)-1-propylamine
43108-00-5

N,N-dimethyl-3-(triethoxysilyl)-1-propylamine

B

2-dimethylaminopropyltriethoxysilane

2-dimethylaminopropyltriethoxysilane

Conditions
ConditionsYield
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex; ammonium bicarbonate In toluene at 55℃; for 17h; Reagent/catalyst;A 92.3%
B 6.8%
diazoacetone
2684-62-0

diazoacetone

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

3-dimethylamino-5-hexen-2-one
60416-73-1

3-dimethylamino-5-hexen-2-one

Conditions
ConditionsYield
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h;92%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

1-diazo-3-methylbutan-2-one
14088-55-2

1-diazo-3-methylbutan-2-one

4-(N,N-dimethylamino)-2-methyl-6-hepten-3-one

4-(N,N-dimethylamino)-2-methyl-6-hepten-3-one

Conditions
ConditionsYield
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h;92%
carbonyl(5,10,15,20-tetraphenylporphyrinato)ruthenium(II) In toluene at 50℃; for 5h;85%
N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

(dimethoxy)methylsilane
16881-77-9

(dimethoxy)methylsilane

A

2-dimethylaminopropylmethyldimethoxysilane

2-dimethylaminopropylmethyldimethoxysilane

B

<3-(dimethylamino)propyl>dimethoxymethylsilane
67353-42-8

<3-(dimethylamino)propyl>dimethoxymethylsilane

Conditions
ConditionsYield
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex; ammonium bicarbonate In toluene at 45℃; for 12h; Reagent/catalyst;A 8%
B 91.4%
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