CAS No.111-26-2,Hexylamine Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

Dayangchem’s 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. DayangChem can provide different quantiti

Hexylamine suppliers in China

Cas:111-26-2

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Simagchem Corporation

Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our

High quality N-Hexylamine supplier in China

Cas:111-26-2

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Hefei TNJ chemical industry co.,ltd

Properties Hexylamine is a kind of water-white liquid with an amine-like odor. Flash point 85°F. Boiling point 132°F. Less dense than water and poorly soluble in swater. Hence floats on water. May be toxic by inhalation, ingestion or ski

Hexylamine

Cas:111-26-2

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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

Hexylamine

Cas:111-26-2

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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 N-Hexylamine

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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

1-Aminohexane

Cas:111-26-2

Min.Order:5 Kiloliter

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Henan Tianfu Chemical Co., Ltd.

Henan Tianfu Chemical Co., Ltd. is located in Zhengzhou High-tech Development Zone with import and export license. We passed ISO 9001:2008 in 2009, and won "High-tech Enterprise" by provincial government in 2013.The objective of the com

TIANFU-CHEM - Hexylamine

Cas:111-26-2

Min.Order:1 Gram

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Henan Sinotech Import&Export Corporation

ECNumber 203-851-8 BeilsteinRegistryNumber 1731298 Description Solubility:14 g/l (20°C). BP

Hexylamine CAS:111-26-2

Cas:111-26-2

Min.Order:5 Metric Ton

FOB Price: $1.0 / 2.0

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Lonwin Chemical Group Limited

Hexylamine CAS：111-26-2 Specification properties hexylamine is a kind of water-white liquid with an amine-like odor. flash point 85°f. boiling point 132°f. less dense than water and poorly soluble in swater. hence floats on water. may be

Factory supply Hexylamine

Cas:111-26-2

Min.Order:1 Kilogram

FOB Price: $100.0 / 150.0

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Changchun Artel lmport and Export trade company

Price, service, company and transport advantage: 1.place of origin china with super quality by reasonable price. 2.fast delivery by safe express way to all the country. 3.has a number of highly qualified engineers and experts to p

BEST PRICE!/hexylamine CAS NO.111-26-2

Cas:111-26-2

Min.Order:100 Gram

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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

Hexylamine

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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

1-Hexanamine

Cas:111-26-2

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Henan Wentao Chemical Product Co., Ltd.

We are leading fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...)

HexylamineCAS NO.: 111-26-2

Cas:111-26-2

Min.Order:1 Kilogram

FOB Price: $5.0

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Hangzhou Ocean Chemical Co., Ltd.

★.Best quality according to requirement ★.Competitive price in China market ★.Mature Technical support ★.Professional logistic support ★.Shortest delivery time . Appearance:Colorless liquid with ammonia flavor Storage:Store in dry, cool and ventilate

Aminohexane high purity 111-26-2 manufacturer best priceN-n-hexylamine

Cas:111-26-2

Min.Order:1 Kilogram

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Hangzhou Huarong Pharm Co., Ltd.

Hangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu

Hexylamine

Cas:111-26-2

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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

hexylamine

Cas:111-26-2

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Hangzhou Dingyan Chem Co., Ltd

R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates

1-Hexanamine

Cas:111-26-2

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Wuhan Fortuna Chemical Co.,Ltd

stable supply&competitive price Storage:Available Package:25KG Or as client requirement Application:Important pharm intermediate Transportation:By air or By sea

Hexylamine

Cas:111-26-2

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Aecochem Corp.

Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS

N-Hexylamine

Cas:111-26-2

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Zhuozhou Wenxi import and Export Co., Ltd

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

factory supply CAS 111-26-2 with competitive price

Cas:111-26-2

Min.Order:1 Kilogram

FOB Price: $112.0

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Antimex Chemical Limied

HexylamineAppearance:colourless liquid Storage:room temperature Package:as required Application:111-26-2 Transportation:by sea/ by express

Hexylamine

Cas:111-26-2

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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

Hexylamine

Cas:111-26-2

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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

Hexylamine

Cas:111-26-2

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Chemsigma International Co.,Ltd.

bulk?production Application:Pharmaceutical intermediates

Hexylamine

Cas:111-26-2

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HWRK Chem

in storeAppearance:Colorless liquid Package:1kg Application:Organic Chemicals

Hexylamine

Cas:111-26-2

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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#111-26-2;CAT#A802331

Cas:111-26-2

Min.Order:10 Milligram

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HENAN SUNLAKE ENTERPRISE CORPORATION

Henan Sunlake Enterprise Corporation Our Advantages 1, Any inquiry about ch

Hexylamine

Cas:111-26-2

Min.Order:1 Kilogram

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Shaanxi Mingqi Chemical Co., Ltd

Product Name Hexylamine Synonyms Hexylamine;1-Aminohexane CAS: 111-26-2 MF: - MW: - EINECS: - Produc

Factory Supply Top quality Hexylamine in stock

Cas:111-26-2

Min.Order:1 Kilogram

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Changzhou Extraordinary Pharmatech co.,LTD

Changzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa

1-Hexaneamine

Cas:111-26-2

Min.Order:1 Gram

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Zibo Kunran Enterprises Co. LTD

1. Factory steady offer directly; 2. More than 10 years of production and process improved experience; 3. Professional hazard chemical Logistics; 4. Reliable quality assurance 5. Punctual delivery time Appearance:A colorless clear liquid wi

Hexylamine

Cas:111-26-2

Min.Order:150 Kilogram

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Synthetic route

: 646-14-0
1-nitrohexane

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With carbon monoxide; Au/TiO2-VS; water In ethanol at 25℃; under 3800.26 Torr; for 5.5h; Autoclave; chemoselective reaction;	100%
With trichlorosilane; N-ethyl-N,N-diisopropylamine In acetonitrile at 15℃; for 18h;	100%
With 5%-palladium/activated carbon; hydrogen In para-xylene; isopropyl alcohol at 25℃; under 760.051 Torr; Reagent/catalyst; Temperature;	100%

: 628-73-9
hexanenitrile

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With triethylamine alane In tetrahydrofuran for 0.5h; Ambient temperature;	96.5%
With hydrogen; aluminum oxide; silica gel; nickel In methanol; ammonia at 160℃; under 7600 Torr; for 1h;	95%
With palladium; hydrogen In ethanol at 50℃; under 3750.38 Torr; for 24h; Temperature;	90%

: 20320-48-3
N-hexylphthalimide

A: 111-26-2
hexan-1-amine

B: 612-14-6
phthalyl alcohol

Conditions

Conditions	Yield
With C25H19BrMnN2O2P; potassium tert-butylate; hydrogen In tetrahydrofuran at 130℃; under 22502.3 Torr; for 48h; Inert atmosphere; Glovebox; Autoclave; Green chemistry;	A 95% B 90%
With [Ru(PtBuNNHtBu)H(CO)Cl]; potassium tert-butylate; hydrogen In tetrahydrofuran at 110℃; under 15001.5 Torr; for 24h; Autoclave;

: 628-02-4
Caproamide

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With triethylamine alane In tetrahydrofuran for 48h; Ambient temperature;	93%
With hydrogen; hexarhodium hexadecacarbonyl; decacarbonyldirhenium(0) In 1,2-dimethoxyethane; diethylamine at 180℃; under 76000 Torr; for 8h;	76%
With sodium tetrahydroborate; methanesulfonic acid In dimethyl sulfoxide	74%

: 6926-45-0
1-azidohexane

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With formiate d'ammonium; palladium on activated charcoal In methanol Ambient temperature;	93%
With formiate d'ammonium; palladium on activated charcoal In methanol Product distribution; Ambient temperature;	93%
With sodium tetrahydroborate; lithium chloride In tetrahydrofuran at 0 - 35℃; for 0.5h;	90%

: 628-73-9
hexanenitrile

A: 111-26-2
hexan-1-amine

B: 143-16-8
dihexylamine

Conditions

Conditions	Yield
With hydrogen; aluminum oxide; carbon monoxide In cyclohexane at 120℃; under 152000 Torr; for 2.73333h;	A 91% B 9%
With ammonium hydroxide; chloro(1,5-cyclooctadiene)rhodium(I) dimer; hydrogen at 100℃; under 20686.5 Torr; for 24h; Autoclave; Green chemistry; chemoselective reaction;

: 66-25-1
hexanal

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With ammonium formate In toluene at 80℃; for 4h; Reagent/catalyst; Inert atmosphere; chemoselective reaction;	91%
With ammonium hydroxide; ammonium acetate; hydrogen; [Ru(cod)Cl]2; trisodium tris(3-sulfophenyl)phosphine In toluene at 145℃; under 48754.9 Torr; for 10h;	45 % Chromat.
Multi-step reaction with 3 steps 1: 1,4-dioxane / 0.5 h / 60 °C / Inert atmosphere 2: copper(l) iodide; caesium carbonate / 1,4-dioxane / 3.5 h / 110 °C / Inert atmosphere 3: hydrazine hydrate / 1,4-dioxane / 110 °C / Inert atmosphere View Scheme

: 628-73-9
hexanenitrile

A: 111-26-2
hexan-1-amine

B: 143-16-8
dihexylamine

C: 102-86-3
tri-n-hexylamine

Conditions

Conditions	Yield
With hydrogen; Pt/Al2O3 In cyclohexane at 120℃; under 152000 Torr; for 2.66667h;	A 5.6% B 89% C 5.4%
With hydrogen; aluminum oxide; nickel In cyclohexane at 120℃; under 152000 Torr; for 0.416667h; Product distribution; variation of temperature, time, catalyst;	A 57.5% B 41.3% C 1.2%

...Expand

: 207558-25-6
hexylcarbamic acid tert-butyl ester

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With nitric acid In dichloromethane at 0℃; for 1h;	89%

: 20320-48-3
N-hexylphthalimide

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With hydrazine hydrate In 1,4-dioxane at 110℃; Gabriel Amine Synthesis; Inert atmosphere;	84%
With potassium hydroxide; sodium hydroxide at 200 - 280℃; Yield given;

: 6621-59-6
6-bromo-1-hexanenitrile

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With indium(III) chloride; sodium tetrahydroborate In tetrahydrofuran at 25℃; for 4h; Inert atmosphere;	76%

: 142-62-1
hexanoic acid

A: 110-54-3
hexane

B: 111-26-2
hexan-1-amine

C: 143-16-8
dihexylamine

D: 628-02-4
Caproamide

E: 10264-29-6
N-(n-hexyl)hexanamide

Conditions

Conditions	Yield
Stage #1: hexanoic acid With cyclopentyl methyl ether; ammonia at 200℃; under 4500.45 Torr; Sealed tube; Green chemistry; Stage #2: With cyclopentyl methyl ether; ammonia; hydrogen at 200℃; under 42004.2 Torr; for 6.5h; Cooling with ice; Green chemistry;	A n/a B 75% C 13% D n/a E 6%

...Expand

: 646-14-0
1-nitrohexane

A: 111-26-2
hexan-1-amine

B: 90422-09-6
N-hydroxyhexan-1-amine

Conditions

Conditions	Yield
With 5%-palladium/activated carbon; hydrogen In para-xylene; isopropyl alcohol at 25℃; under 760.051 Torr; for 4h; Reagent/catalyst;	A 26% B 72%
With 5%-palladium/activated carbon; hydrogen In isopropyl alcohol at 20℃; under 750.075 Torr; for 2h;	A 6 %Spectr. B 94 %Spectr.

: 16343-08-1
hexylboronic acid

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With N-Bromosuccinimide; CYANAMID; bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile at 20℃; for 2h; chemoselective reaction;	72%
With N-Bromosuccinimide; N-methoxylamine hydrochloride; bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile at 20℃; for 3h;	65%

: 127146-31-0
1-hexyl-dimethylborane

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With ammonium hydroxide; sodium hypochlorite In water 1.) 0 deg C, 5-10 min, 2.) 0 deg C -> room temperature;	67%

: 64-18-6
formic acid

: 646-14-0
1-nitrohexane

A: 111-26-2
hexan-1-amine

B: 2591-78-8
N-hexylformamide

Conditions

Conditions	Yield
With cobalt nanoparticles anchoring on nitrogen doped carbon, pyrolysis at 700 °C In acetonitrile at 110℃; under 750.075 Torr; for 5h; Inert atmosphere; chemoselective reaction;	A n/a B 59.2%

...Expand

: 146303-94-8
hexylmethylphenylborane

A: 111-26-2
hexan-1-amine

B: 62-53-3
aniline

Conditions

Conditions	Yield
With ammonium hydroxide; sodium hypochlorite In diethyl ether at 25℃; for 0.5h;	A 38% B 56%

: 124-04-9
Adipic acid

A: 105-60-2
caprolactam

B: 111-49-9
hexamethylene imine

C: 21920-79-6
6-(azepan-1-yl)hexan-1-amine

D: 111-26-2
hexan-1-amine

E: 110-58-7
1-pentanamine

Conditions

Conditions	Yield
Stage #1: Adipic acid With cyclopentyl methyl ether; ammonia at 200℃; under 4500.45 Torr; Sealed tube; Green chemistry; Stage #2: With cyclopentyl methyl ether; ammonia; hydrogen at 200℃; under 42004.2 Torr; for 6.5h; Cooling with ice; Green chemistry;	A 39% B 53% C 4% D 2% E 2%

...Expand

: 628-62-6
heptanamide

A: 111-26-2
hexan-1-amine

B: 111-14-8
oenanthic acid

Conditions

Conditions	Yield
With sodium hydroxide; sodium persulfate; sodium chloride In water at 85 - 90℃; for 7h;	A 35% B 52%
With sodium hydroxide; sodium persulfate; sodium chloride In water at 85 - 90℃; for 7h;	A 35% B 49%

(n-C6H13)3ZnMgBr: (n-C6H13)3ZnMgBr

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
Stage #1: (n-C6H13)3ZnMgBr With O-Methylhydroxylamin In tetrahydrofuran at 20℃; for 3h; Amination; Stage #2: With ammonia; water; ammonium chloride at 20℃; for 2h; Hydrolysis;	50%

: 67-56-1
methanol

: 6926-45-0
1-azidohexane

A: 111-26-2
hexan-1-amine

B: 4385-04-0
N,N-dimethylhexylamine

C: 42870-70-2
N-methylhexan-1-amine hydrochloride

Conditions

Conditions	Yield
Stage #1: methanol; 1-azidohexane With trans-RuCl(phenpyra-Me)(PPh3)2PF6; sodium hydroxide at 125℃; for 5h; Sealed tube; Inert atmosphere; Glovebox; Stage #2: With hydrogenchloride	A 10 %Chromat. B 12 %Chromat. C 42%

...Expand

: 102-86-3
tri-n-hexylamine

A: 111-26-2
hexan-1-amine

B: 143-16-8
dihexylamine

C: 34695-21-1
N-hexylidenehexan-1-amine

Conditions

Conditions	Yield
With dicarbonyl(chloro)(η5-pentaphenylcyclopentadienyl)ruthenium(II); ammonia In tert-Amyl alcohol at 170℃; for 23.5h; Inert atmosphere; Schlenk technique; Autoclave;	A 12% B 8% C 41.5%

...Expand

: 13822-55-4
di(n-hexyl)zinc

(: (

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
Stage #1: di(n-hexyl)zinc; ( With O-Methylhydroxylamin In tetrahydrofuran at 20℃; for 3h; Amination; Stage #2: With ammonia; water; ammonium chloride at 20℃; for 2h; Hydrolysis;	35%

: 631-61-8
ammonium acetate

: 111-27-3
hexan-1-ol

A: 592-41-6
1-hexene

B: 111-26-2
hexan-1-amine

C: 142-92-7
1-hexyl acetate

D: 7501-79-3
N-hexylacetamide

E: 66-25-1
hexanal

Conditions

Conditions	Yield
With water at 400℃; for 1h; Product distribution / selectivity;	A 29.4 %Chromat. B 1.9 %Chromat. C 4 %Chromat. D 30.8% E 1.3 %Chromat.
With water at 380 - 420℃; for 0.05 - 1h; Product distribution / selectivity;	A 0.2 - 11.29 %Chromat. B 0.21 - 6.52 %Chromat. C 1.53 - 10.25 %Chromat. D 7.03 - 78.52 %Chromat. E 0.36 - 1.28 %Chromat.

...Expand

: 97308-22-0
N-(t-butyldimetylsilyl)aziridine

(Bu)2CuLi: (Bu)2CuLi

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In tetrahydrofuran	30%

: 10264-29-6
N-(n-hexyl)hexanamide

A: 111-26-2
hexan-1-amine

B: 143-16-8
dihexylamine

C: 111-27-3
hexan-1-ol

Conditions

Conditions	Yield
With ruthenium(1,1,1-tris(di(3,5-dimethylphenyl)phosphinomethyl)ethane)(η4-trimethylenemethane); tris(pentafluorophenyl)borate; hydrogen In tetrahydrofuran at 160℃; under 75007.5 Torr; for 16h;	A 7.6% B 26.03% C 5.4%
With aluminium(III) triflate; ruthenium(1,1,1-tris(di(3,5-dimethylphenyl)phosphinomethyl)ethane)(η4-trimethylenemethane); hydrogen In tetrahydrofuran at 160℃; under 75007.5 Torr; for 16h;	A 5.4% B 19.04% C 13.1%

...Expand

: 143-16-8
dihexylamine

A: 628-73-9
hexanenitrile

B: 111-26-2
hexan-1-amine

C: 102-86-3
tri-n-hexylamine

Conditions

Conditions	Yield
With dicarbonyl(chloro)(η5-pentaphenylcyclopentadienyl)ruthenium(II); ammonia In tert-Amyl alcohol at 170℃; for 23.5h; Inert atmosphere; Schlenk technique; Autoclave;	A 8.5% B 25% C 11%

...Expand

: 124-38-9
carbon dioxide

: 62-53-3
aniline

: 111-26-2
hexan-1-amine

Conditions

Conditions	Yield
With Pd/C; hydrogen In ethanol at 130℃; for 24h;	11%

: 110-89-4
piperidine

: 41495-45-8
1-Pentyl-1-hexylamine

A: 10324-58-0
1-pentylpiperidine

B: 7335-01-5
1-hexylpiperidine

C: 111-26-2
hexan-1-amine

D: 143-16-8
dihexylamine

E: 110-58-7
1-pentanamine

F: 2050-92-2
Di-n-amylamine

Conditions

Conditions	Yield
With hydrogen; sulphidized CoO-MoO3 at 300℃; under 45003.6 Torr; for 1h; Mechanism; Product distribution;	A 5.5% B 8.5% C 4% D 3% E 1% F 2.5%

...Expand

: 111-26-2
hexan-1-amine

: 100-52-7
benzaldehyde

: 19340-96-6
N-benzylidenehexylamine

Conditions

Conditions	Yield
at 20℃; for 2h;	100%
With ethanol; potassium carbonate
With aluminum oxide for 2h; Ambient temperature;

: 111-26-2
hexan-1-amine

: 598-21-0
2-Bromoacetyl bromide

: 5439-32-7
2-bromo-N-hexylethanamide

Conditions

Conditions	Yield
With potassium carbonate In dichloromethane; water at 5 - 20℃; for 4h;	100%
With potassium carbonate In dichloromethane; water at 4 - 20℃; for 4.5h;	100%
With potassium carbonate In dichloromethane; water at 0 - 20℃; for 6.5h;	100%

: 506-68-3
bromocyane

: 111-26-2
hexan-1-amine

: 15784-76-6
n-hexylcyanamide

Conditions

Conditions	Yield
	100%
In tetrahydrofuran; diethyl ether at 0℃; for 3.5h; Inert atmosphere;	80%
With sodium carbonate In tetrahydrofuran at -20 - 0℃;

: 67-56-1
methanol

: 111-26-2
hexan-1-amine

: 4385-04-0
N,N-dimethylhexylamine

Conditions

Conditions	Yield
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) at 100℃;	100%
With tris(triphenylphosphine)ruthenium(II) chloride at 180℃; for 7h;	88%
With C53H41ClN3OP2Ru(1+)*F6P(1-); sodium methylate at 110℃; for 24h; Inert atmosphere; Glovebox; Schlenk technique; Sealed tube; Green chemistry;	77%

: 111-26-2
hexan-1-amine

: 7677-24-9
trimethylsilyl cyanide

: 87367-65-5
4,4'-[decane-1,10-diylbis(oxy)]dibenzaldehyde

: 145100-47-6
(4-{10-[4-(Cyano-hexylamino-methyl)-phenoxy]-decyloxy}-phenyl)-hexylamino-acetonitrile

Conditions

Conditions	Yield
In dichloromethane for 120h;	100%

...Expand

: 111-26-2
hexan-1-amine

: 64-19-7
acetic acid

: 7501-79-3
N-hexylacetamide

Conditions

Conditions	Yield
triphenylantimony(V) diacetate In pyridine at 100℃; for 10h;	100%
With silica In toluene for 8h; Dean-Stark; Reflux; Green chemistry;	99%
tetraphosphorus decasulfide; triphenyl antimony oxide In benzene at 40℃; for 5h;	90%
With HOBt-6-carboxamidomethyl polystyrene; dicyclohexyl-carbodiimide 1.) CH2Cl2, 25 deg C, 2.) CH2Cl2, 25 deg C, 4 h; Yield given. Multistep reaction;
With Sc(OTf)3 immobilized onto mesoporous at 80℃; for 24h; Product distribution; Further Variations:; Reagents;

: 111-26-2
hexan-1-amine

: 4637-24-5
N,N-dimethyl-formamide dimethyl acetal

: 85599-94-6
N2-n-hexyl-N1,N1-dimethylformamidine

Conditions

Conditions	Yield
at 60℃;	100%

: 111-26-2
hexan-1-amine

: 105-54-4
butanoic acid ethyl ester

: 10264-17-2
N-hexylbutanamide

Conditions

Conditions	Yield
at 40℃; for 1h; lipase SP 382 (from Candida sp.);	100%

: 111-26-2
hexan-1-amine

: 78-92-2, 15892-23-6
iso-butanol

: 20007-05-0
N-(sec-butyl)hexan-1-amine

Conditions

Conditions	Yield
With Zr6O4(OH)4(BDC-NH2)5.7([LIr]BF4)0.3 at 80℃; for 24h; Catalytic behavior; Autoclave; Green chemistry;	100%
dihydridotetrakis(triphenylphosphine)ruthenium In neat (no solvent) at 180℃; for 6h;	52 % Chromat.

: 111-26-2
hexan-1-amine

: 624-31-7
4-tolyl iodide

: 56506-60-6
N-(4-methylphenyl)hexylamine

Conditions

Conditions	Yield
With 2-(2-methyl-1-oxopropyl)cyclohexanone; caesium carbonate; copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 1.5h;	100%
With caesium carbonate; copper(I) bromide In dimethyl sulfoxide at 55℃; for 24h; Ullmann coupling;	87%
With tetra(n-butyl)ammonium hydroxide; copper(l) chloride In water at 80℃; for 24h; Inert atmosphere;	86%

: 111-26-2
hexan-1-amine

: 66046-61-5
2-chloro-3-methyl-1-oxa-3-aza-2-phosphacyclopentane 2-oxide

: 184417-25-2
Hexyl-(3-methyl-2-oxo-2λ5-[1,3,2]oxazaphospholidin-2-yl)-amine

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 17h; Ambient temperature;	100%

: 111-26-2
hexan-1-amine

: 180716-18-1
2-(bromomethyl)-7-(benzyloxy)chroman

: 198986-38-8
(7-Benzyloxy-chroman-2-ylmethyl)-hexyl-amine

Conditions

Conditions	Yield
at 100℃; for 2h;	100%

: 591-50-4
iodobenzene

: 111-26-2
hexan-1-amine

: 4746-32-1
N-hexylaniline

Conditions

Conditions	Yield
With 2-(2-methyl-1-oxopropyl)cyclohexanone; caesium carbonate; copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 1.16667h;	100%
With copper(l) iodide; 1-(5,6,7,8-tetrahydroquinolin-8-yl)ethan-1-one; caesium carbonate In N,N-dimethyl-formamide at 25℃; for 10h; Ullmann condensation; Inert atmosphere;	97%
With caesium carbonate; copper(I) bromide In dimethyl sulfoxide at 55℃; for 24h; Ullmann coupling;	91%

: 917-92-0
2,2-dimethyl-3-butyne

: 111-26-2
hexan-1-amine

: 201230-82-2
carbon monoxide

: (E)-4,4-Dimethyl-pent-2-enoic acid hexylamide

Conditions

Conditions	Yield
Stage #1: 3,3-Dimethylbut-1-yne; carbon monoxide With quinoline; tri(2-furyl)germane; tris(2,4-di-tert-butylphenyl)phosphite; bis(η3-allyl-μ-chloropalladium(II)) In toluene at 20℃; under 760.051 Torr; for 5.5h; Stage #2: hexan-1-amine; dmap In toluene at 70℃; for 6h; Further stages.;	100%

...Expand

: 57-48-7
D-Fructose

: 111-26-2
hexan-1-amine

: 1,2-dideoxy-1,2-di-n-hexylamino-D-(N)-β-glucoside

Conditions

Conditions	Yield
With 4 A molecular sieve; zinc(II) chloride at -20℃; for 48h;	100%

: 111-26-2
hexan-1-amine

: 1145-80-8
N-(benzyloxycarbonyl)-L-serine

: 138739-31-8
((S)-1-Hexylcarbamoyl-2-hydroxy-ethyl)-carbamic acid benzyl ester

Conditions

Conditions	Yield
With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In N,N-dimethyl-formamide	100%

: 111-26-2
hexan-1-amine

: 696-62-8
para-iodoanisole

: 16664-54-3
N-(n-hexyl)-p-methoxyaniline

Conditions

Conditions	Yield
With 2-(2-methyl-1-oxopropyl)cyclohexanone; caesium carbonate; copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 1.83333h;	100%
With copper(l) iodide; 1-(5,6,7,8-tetrahydroquinolin-8-yl)ethan-1-one; caesium carbonate In N,N-dimethyl-formamide at 25℃; for 12h; Ullmann condensation; Inert atmosphere;	97%
With copper(l) iodide; 1-tetralone oxime; potassium hydroxide In water at 25℃; for 36h; Sealed tube; Inert atmosphere; Green chemistry;	94%

: 111-26-2
hexan-1-amine

: 6068-70-8
triphenylacetyl chloride

: N-hexyl-2,2,2-triphenyl-acetamide

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane for 48h;	100%

: 111-26-2
hexan-1-amine

: 1489-69-6
Cyclopropanecarboxaldehyde

: [1-Cyclopropyl-meth-(E)-ylidene]-hexyl-amine

Conditions

Conditions	Yield
With magnesium sulfate In dichloromethane Heating;	100%

: 637-87-6
1-Chloro-4-iodobenzene

: 111-26-2
hexan-1-amine

: 56506-62-8
N-(4-chlorophenyl)-n-hexylamine

Conditions

Conditions	Yield
With 2-(2-methyl-1-oxopropyl)cyclohexanone; caesium carbonate; copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 0.833333h;	100%
With copper(l) iodide; 1-tetralone oxime; potassium hydroxide In water at 25℃; for 18h; Sealed tube; Inert atmosphere; Green chemistry;	92%
With copper(l) iodide; 1-(5,6,7,8-tetrahydroquinolin-8-yl)ethan-1-one; caesium carbonate In N,N-dimethyl-formamide at 25℃; for 12h; Ullmann condensation; Inert atmosphere;	91%

: 111-26-2
hexan-1-amine

: 3058-39-7
4-iodobenzonitrile

: 4-(N-Hexyl)aminobenzonitrile

Conditions

Conditions	Yield
With 2-(2-methyl-1-oxopropyl)cyclohexanone; caesium carbonate; copper(l) iodide In N,N-dimethyl-formamide at 25℃; for 0.666667h;	100%
With copper(l) iodide; 1-(5,6,7,8-tetrahydroquinolin-8-yl)ethan-1-one; caesium carbonate In N,N-dimethyl-formamide at 25℃; for 10h; Ullmann condensation; Inert atmosphere;	95%
With copper(l) iodide; 1-tetralone oxime; potassium hydroxide In water at 25℃; for 18h; Sealed tube; Inert atmosphere; Green chemistry;	95%

: 111-26-2
hexan-1-amine

: 141-97-9
ethyl acetoacetate

: ethyl 4-(N-hexylamino)but-2-enoate

Conditions

Conditions	Yield
With erbium(III) triflate In dichloromethane at 20℃; for 2h;	100%

: 868-84-8
S,S-dimethyl dithiocarbonate

: 111-26-2
hexan-1-amine

: 120904-15-6
S-methyl N-hexylthiocarbamate

Conditions

Conditions	Yield
In water at 20 - 25℃; for 2h;	100%

: 111-26-2
hexan-1-amine

: H2Ti4O9*1.9H2O

: 1.1C6H13NH3(1+)*0.9H(1+)*Ti4O9(2-)*2.4H2O = (C6H13NH3)1.1H0.9Ti4O9*2.4H2O

Conditions

Conditions	Yield
In not given heating to 100°C for 2 days; centrifugation; filtration; washing (ethanol, acetone); drying in vac. for 1 h; chem. anal.; TGA; electron diffraction;	100%
In not given stirring for 6 days at 50°C; centrifugation; filtration; washing (ethanol, acetone); drying in vac. for 1 h; chem. anal.; TGA; electron diffraction;

: 111-26-2
hexan-1-amine

: 1042070-13-2
C16H21NO7

: 1042070-07-4
C19H26N2O5

Conditions

Conditions	Yield
In methanol at 20℃;	100%

: 111-26-2
hexan-1-amine

: 60-12-8
2-phenylethanol

: 10264-30-9
N-hexyl-2-phenylacetamide

Conditions

Conditions	Yield
With cyclooctadiene ruthenium(II) dichloride; potassium tert-butylate; 1,3-diisopropyl-1H-imidazol-3-ium chloride; tricyclopentylphosphonium tetrafluoroborate In toluene for 24h; Inert atmosphere; Reflux;	100%
With dichloro(1,5-cyclooctadiene)ruthenium(II); potassium tert-butylate; 1,3-diisopropyl-1H-imidazol-3-ium chloride; tricyclopentylphosphonium tetrafluoroborate In toluene at 110℃; for 24h; Inert atmosphere;	100%
With pyridine; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium hydride; 1,3-di(propan-2-yl)-1H-imidazol-3-ium bromide In toluene for 36h; Inert atmosphere; Reflux;	98%

: 111-26-2
hexan-1-amine

: 100-51-6
benzyl alcohol

: 25468-44-4
N-benzylhexylamine

Conditions

Conditions	Yield
With Zr6O4(OH)4(BDC-NH2)5.7([LIr]BF4)0.3 at 120℃; for 0.5h; Catalytic behavior; Temperature; Microwave irradiation; Green chemistry;	100%
With lithium hydroxide In neat (no solvent) at 120℃; for 24h; Inert atmosphere;	94%
With palladium nanoparticles embedded in the solid matrix of tetrabutylammonium bromide synthetized in supercritical carbon dioxide at 140℃; Sealed tube; Inert atmosphere; Green chemistry;	88%

: 111-26-2
hexan-1-amine

: 5336-08-3
D-Ribono-1,4-lactone

: 1190205-35-6
N-hexyl-D-ribonamide

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 20℃; for 1h;	100%
In N,N-dimethyl-formamide at 20℃; for 1h;

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