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Cas:2432-74-8
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inquiryOur advantages: 1, High quality with competitive price: 1) Standard:BP/USP/EP/Enterprise standard 2) All Purity≥99% 3) We are manufacturer and can provide high quality products with factory price. 2, Fast and safe delivery 1) Parcel can be
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Cas:2432-74-8
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inquiry6-AMINO CAPRONITRILE CAS:2432-74-8 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 inte
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Min.Order:1 Gram
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inquiryHenan 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
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
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inquiryZibo 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
Cas:2432-74-8
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inquiry6-AMINO CAPRONITRILE Basic information Product Name: 6-AMINO CAPRONITRILE Synonyms: 6-amino-hexanenitril;6-amino
Cas:2432-74-8
Min.Order:1 Metric Ton
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Type:Lab/Research institutions
inquiryR & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
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
1. Product advantages? High purity, all above 98.5%, no impurities after dissolution? We will test each batch to ensure quality? OEM and private brand services designed for free? Various cap colors available? We can also provide MT1 peptide powder2.
Hexanenitrile, 6-amino-Appearance:detailed see specifications Storage:Keep away of light, cool place Package:25kg/drum;200kg/drum Application:Used in Synthesis, Pharmaceuticals and other fields Transportation:Sea/air/courier
Hexanenitrile, 6-amino- cas 2432-74-8Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
Best quality with low price Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Shanghai
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right
Cas:2432-74-8
Min.Order:0
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Type:Trading Company
inquiryXuzhou Jinhe Technology Co., Ltd. is an enterprise mainly engaged in pharmaceutical R&D outsourcing services. Taking advantage of rich professional experience and resource advantages in chemical synthesis, pharmaceutical chemistry and biotechno
Cas:2432-74-8
Min.Order:1 Gram
FOB Price: $1.5
Type:Lab/Research institutions
inquiryAt Share Chemical Company, we scrupulously abide by our policy of “Excellent Quality at a Reasonable Price”. We strive to satisfy all of our customers by providing the finest quality products supported by the finest in customer servi
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
Joyinchem have been committed to chemical supply for several years and have built good cooperation records with multinational chemical corporations and importers from all over the world. Our services include:-Spot goods-Contract manufacturing-Custom
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 6-AMINO CAPRONITRILE, CAS:2432-74-8 with the most competitive price and the best qual
Hexanenitrile, 6-amino-Appearance:Off white to slight yellow solid Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By courie
Supply top quality products with a reasonable price Application:api
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
Manufacturer,strong R&D,professional team Storage:Store in a cool, dry place. Store in a tightly closed container. Package:according to your requirement Application:ZhiShang Chemical is owned by ZhiShang Group, is a professional new-type chemicals en
Conditions | Yield |
---|---|
With manganese(IV) oxide; ammonia at 200℃; under 9750.98 Torr; Reagent/catalyst; Temperature; Pressure; | 99% |
With ammonia; silica gel; copper at 360℃; |
2-Trimethylsilanyl-ethanesulfonic acid (5-cyano-pentyl)-amide
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With cesium fluoride In N,N-dimethyl-formamide at 95℃; for 40h; | 83% |
C12H21N3
A
caprolactam
B
1-amino-5-cyanopentane
C
ethyl 6-aminohexanoate
Conditions | Yield |
---|---|
With water; titanium(IV) oxide In ethanol at 230℃; under 60006 Torr; | A 80% B n/a C n/a |
Conditions | Yield |
---|---|
With Rh/Al2O3; hydrogen In ethanol at 80℃; for 6h; | A 24.4% B 75.6% |
With hydrogen; active elemental iron component In ammonia at 70 - 220℃; under 75007.5 - 300030 Torr; | |
Stage #1: hexanedinitrile With potassium hydroxide; hydrogen; nickel at 50℃; under 15001.5 Torr; Stage #2: With phosphoric acid Purification / work up; |
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; nickel at 169.9℃; under 760 Torr; | 75% |
With nickel-aluminium oxide; ammonia at 120℃; under 102971 - 154457 Torr; Hydrogenation; | |
With cobalt kieselguhr; ammonia at 120℃; under 102971 - 154457 Torr; Hydrogenation; |
1-azido-5-cyano-pentane
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With sodium tetrahydroborate; cobalt(II) chloride In water at 20℃; for 1h; | 66% |
hexanedinitrile
A
1,6-Hexanediamine
B
1-amino-5-cyanopentane
C
2-iminocyclopentanecarbonitrile
Conditions | Yield |
---|---|
With potassium hydroxide; hydrogen; nickel at 50℃; under 15001.5 Torr; Purification / work up; | A n/a B n/a C 12% |
Conditions | Yield |
---|---|
With thionyl chloride |
hexanedinitrile
A
hexamethylene imine
B
1,6-Hexanediamine
C
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; nickel at 169.9℃; under 760 Torr; Product distribution; varying space velocity of catalysts; | |
With hydrogen; nickel monophosphide; silica gel In ethanol at 199.85℃; under 760 Torr; Product distribution; Further Variations:; Catalysts; | A 16 % Chromat. B 65 % Chromat. C 19 % Chromat. |
With potassium hydroxide; hydrogen; [Ni0.60Mg0.15Al0.25(OH)2](CO32-)0.09(NO3-)0.18 at 79.85℃; under 18751.5 Torr; Product distribution; Further Variations:; Catalysts; Reagents; Temperatures; |
Conditions | Yield |
---|---|
Kochen des Reaktionsprodukts mit Hydrazinhydrat in wss. Aethanol; |
Conditions | Yield |
---|---|
at 95 - 120℃; under 51485.6 - 102971 Torr; Hydrogenation; |
methanol
hexanedinitrile
A
hexamethylene imine
B
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
at 100 - 200℃; under 110326 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
at 95 - 120℃; under 51485.6 - 102971 Torr; Hydrogenation; |
hexanedinitrile
ammonia
A
1,6-Hexanediamine
B
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
je nach den Bedingungen.Hydrogenation; |
hexanedinitrile
butan-1-ol
A
1,6-Hexanediamine
B
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
je nach den Bedingungen.Hydrogenation; |
Cyclohexanone oxime
ammonia
A
caprolactam
B
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
at 250℃; |
hexanedinitrile
A
tetrahydroazepine
B
hexamethylene imine
C
1,6-Hexanediamine
D
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With hydrogen; magnesium oxide; nickel at 109.85℃; Product distribution; Further Variations:; Catalysts; Temperatures; |
Conditions | Yield |
---|---|
With ammonia; hydrogen; iron catalyst, based on magnetite ore and prepared according to Example 2 (a) of DE 19636767 at 30 - 340℃; for 1524h; Conversion of starting material; Compressed gas(es); |
trans,trans-mucononitrile
A
1,6-Hexanediamine
B
hexanedinitrile
C
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With ammonia; hydrogen; Raney nickel In tetrahydrofuran; water at 110℃; under 18100.7 Torr; for 3h; Product distribution / selectivity; Parr reactor; | A 32.8 %Chromat. B 26.3 %Chromat. C n/a |
With ammonia; hydrogen; Raney nickel In tetrahydrofuran; water at 80℃; under 54302 Torr; for 3h; Product distribution / selectivity; Parr reactor; | A 18.4 %Chromat. B 75.2 %Chromat. C n/a |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: sulfuric acid / 18 h / Reflux 2: ammonia / ethanol; water / 336 h / 20 °C 3: trichlorophosphate / Reflux 4: hydrogen; ammonia / Raney nickel / water; tetrahydrofuran / 3 h / 110 °C / 18100.7 Torr / Parr reactor View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: sulfuric acid / 18 h / Reflux 2: iodine / methanol / 60 h / Reflux 3: ammonia / ethanol; water / 336 h / 20 °C 4: trichlorophosphate / Reflux 5: hydrogen; ammonia / Raney nickel / water; tetrahydrofuran / 3 h / 110 °C / 18100.7 Torr / Parr reactor View Scheme | |
Multi-step reaction with 6 steps 1.1: sodium hydroxide / water / 2 h / 90 °C / pH 5.1 1.2: pH 2 2.1: iodine / tetrahydrofuran / 4 h / Reflux 3.1: sulfuric acid / 18 h / Reflux 4.1: ammonia / ethanol; water / 336 h / 20 °C 5.1: trichlorophosphate / Reflux 6.1: hydrogen; ammonia / Raney nickel / water; tetrahydrofuran / 3 h / 110 °C / 18100.7 Torr / Parr reactor View Scheme |
(E,E)-hexa-2,4-dienedioic acid dimethyl ester
A
1,6-Hexanediamine
B
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: ammonia / ethanol; water / 336 h / 20 °C 2: trichlorophosphate / Reflux 3: hydrogen; ammonia / Raney nickel / water; tetrahydrofuran / 3 h / 110 °C / 18100.7 Torr / Parr reactor View Scheme |
(2Z,4E)-2,4-hexadienedioic acid
A
1,6-Hexanediamine
B
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: iodine / tetrahydrofuran / 4 h / Reflux 2: sulfuric acid / 18 h / Reflux 3: ammonia / ethanol; water / 336 h / 20 °C 4: trichlorophosphate / Reflux 5: hydrogen; ammonia / Raney nickel / water; tetrahydrofuran / 3 h / 110 °C / 18100.7 Torr / Parr reactor View Scheme |
hexa-2c,4ξ-dienedioic acid dimethyl ester
A
1,6-Hexanediamine
B
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: iodine / methanol / 60 h / Reflux 2: ammonia / ethanol; water / 336 h / 20 °C 3: trichlorophosphate / Reflux 4: hydrogen; ammonia / Raney nickel / water; tetrahydrofuran / 3 h / 110 °C / 18100.7 Torr / Parr reactor View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: trichlorophosphate / Reflux 2: hydrogen; ammonia / Raney nickel / water; tetrahydrofuran / 3 h / 110 °C / 18100.7 Torr / Parr reactor View Scheme |
hexanedinitrile
A
hexamethylene imine
B
1,6-Hexanediamine
D
1-amino-5-cyanopentane
E
1,8,15-triazapentadecane
Conditions | Yield |
---|---|
With 1-butyl-3-methylimidazolium hydroxide; hydrogen In ethanol at 349.84℃; under 15001.5 Torr; for 6h; Reagent/catalyst; Temperature; Pressure; Time; Flow reactor; Sealed tube; Inert atmosphere; Ionic liquid; |
Conditions | Yield |
---|---|
99.1% | |
99% | |
98.9% |
1-amino-5-cyanopentane
1-chloro-3-methoxy-benzene
6-((3-methoxyphenyl)amino)hexanenitrile
Conditions | Yield |
---|---|
With (2,2′-bis(biphenylphosphino)-1,1′-binaphthalene)Ni(η2-NC-Ph); sodium t-butanolate In toluene at 50℃; for 24h; Inert atmosphere; Glovebox; | 96% |
Conditions | Yield |
---|---|
In hexane at 20℃; | 95% |
1-amino-5-cyanopentane
2-trimethylsilanyl-ethanesulfonyl chloride
2-Trimethylsilanyl-ethanesulfonic acid (5-cyano-pentyl)-amide
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 0℃; for 1.75h; | 94% |
C12H21N3
1-amino-5-cyanopentane
A
caprolactam
B
ethyl 6-aminohexanoate
Conditions | Yield |
---|---|
With water; titanium(IV) oxide In ethanol at 230℃; under 60006 Torr; | A 90% B n/a |
1-amino-5-cyanopentane
2-nitrobenzyl chloride
N-(5-cyanopentyl)-o-nitrobenzamide
Conditions | Yield |
---|---|
With triethylamine In benzene for 5h; Ambient temperature; | 88% |
Conditions | Yield |
---|---|
With bis{1,1’-diphenyl-3,3’-methylenediimidazoline-2,2’-diylidene}nickel(II) dibromide; potassium tert-butylate In 1,4-dioxane at 90℃; for 4h; Catalytic behavior; Reagent/catalyst; Buchwald-Hartwig Coupling; Inert atmosphere; Schlenk technique; | 88% |
With C19H14N4NiO2; potassium tert-butylate In 1,4-dioxane at 90℃; for 4h; Buchwald-Hartwig Coupling; Inert atmosphere; Schlenk technique; | 72% |
Conditions | Yield |
---|---|
With triethylamine In ethanol at 70℃; for 4h; | 86.7% |
1-amino-5-cyanopentane
3-chloro-5-(trifluoromethyl)pyridine
6-((5-(trifluoromethyl)pyridin-3-yl)amino)hexanenitrile
Conditions | Yield |
---|---|
With (2,2′-bis(biphenylphosphino)-1,1′-binaphthalene)Ni(η2-NC-Ph); sodium t-butanolate In toluene at 80℃; for 24h; Inert atmosphere; Glovebox; | 83% |
2-chloro-3-pyridinecarbonitrile
1-amino-5-cyanopentane
2-((5-cyanopentyl)amino)nicotinonitrile
Conditions | Yield |
---|---|
With C19H14N4NiO2; potassium tert-butylate In 1,4-dioxane at 90℃; for 4h; Buchwald-Hartwig Coupling; Inert atmosphere; Schlenk technique; | 80% |
With (2,2′-bis(biphenylphosphino)-1,1′-binaphthalene)Ni(η2-NC-Ph); sodium t-butanolate In toluene at 80℃; for 24h; Inert atmosphere; Glovebox; | 76% |
2-chloropyrazin
1-amino-5-cyanopentane
6-(pyrazin-2-ylamino)hexanenitrile
Conditions | Yield |
---|---|
With (2,2′-bis(biphenylphosphino)-1,1′-binaphthalene)Ni(η2-NC-Ph); sodium t-butanolate In toluene at 80℃; for 24h; Inert atmosphere; Glovebox; | 80% |
1-amino-5-cyanopentane
3-amino-6-iodopyridazine
Conditions | Yield |
---|---|
With potassium phosphate; copper(l) iodide; 4R-4-hydroxyproline In dimethyl sulfoxide at 50℃; for 24h; Inert atmosphere; | 80% |
2-(m-methoxyphenyl)oxirane
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
In isopropyl alcohol for 22h; Heating; | 77% |
2-chloro-4-methoxy-pyridine
1-amino-5-cyanopentane
6-((4-methoxypyridin-2-yl)amino)hexanenitrile
Conditions | Yield |
---|---|
With bis{1,1’-diphenyl-3,3’-methylenediimidazoline-2,2’-diylidene}nickel(II) dibromide; potassium tert-butylate In 1,4-dioxane at 90℃; for 4h; Catalytic behavior; Reagent/catalyst; Buchwald-Hartwig Coupling; Inert atmosphere; Schlenk technique; | 72% |
With C19H14N4NiO2; potassium tert-butylate In 1,4-dioxane at 90℃; for 4h; Buchwald-Hartwig Coupling; Inert atmosphere; Schlenk technique; | 61% |
With (2,2′-bis(biphenylphosphino)-1,1′-binaphthalene)Ni(η2-NC-Ph); sodium t-butanolate In toluene at 80℃; for 24h; Inert atmosphere; Glovebox; | 57% |
1-amino-5-cyanopentane
6-chloro-4-phenyl-pyridazin-3-yl-amine
Conditions | Yield |
---|---|
With dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine; chloro[2-(dicyclohexylphosphino)-3 ,6-dimethoxy-2’,4’, 6’-triisopropyl- 1,1’-biphenyl] [2-(2-aminoethyl)phenyl]palladium(II); lithium hexamethyldisilazane In tetrahydrofuran at 60℃; for 0.416667h; Buchwald-Hartwig Coupling; Inert atmosphere; | 70% |
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 25℃; for 16h; | 69% |
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 25℃; for 16h; |
1-amino-5-cyanopentane
2-chloro-3-trifluoromethyl-pyridine
6-((3-(trifluoromethyl)pyridin-2-yl)amino)hexanenitrile
Conditions | Yield |
---|---|
With C19H14N4NiO2; potassium tert-butylate In 1,4-dioxane at 90℃; for 4h; Buchwald-Hartwig Coupling; Inert atmosphere; Schlenk technique; | 68% |
With (2,2′-bis(biphenylphosphino)-1,1′-binaphthalene)Ni(η2-NC-Ph); sodium t-butanolate In toluene at 80℃; for 24h; Inert atmosphere; Glovebox; | 64% |
3-Chloropyridine
1-amino-5-cyanopentane
6-(pyridin-3-ylamino)hexanenitrile
Conditions | Yield |
---|---|
With (2,2′-bis(biphenylphosphino)-1,1′-binaphthalene)Ni(η2-NC-Ph); sodium t-butanolate In toluene at 80℃; for 24h; Inert atmosphere; Glovebox; | 67% |
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 25℃; for 16h; | 66% |
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 25℃; for 16h; |
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 25℃; for 16h; | 65% |
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 25℃; for 16h; |
5'-[(cyclopropylamino)carbonyl]-4-{[(2,2-dimethylpropyl)amino]carbonyl}-3'-fluoro-2'-methyl-2-biphenylcarboxylic acid
1-amino-5-cyanopentane
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine In N,N-dimethyl-formamide at 20℃; | 65% |
1-amino-5-cyanopentane
oxalic acid diethyl ester
N,N'-(bishexanenitrile) oxalamide
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 12h; | 55% |
(3,4-methylenedioxyphenyl)ethylene oxide
1-amino-5-cyanopentane
6-<2-hydroxy-2-(3,4-metylenedioxyphenyl)ethylamino>hexanonitrile
Conditions | Yield |
---|---|
In isopropyl alcohol for 22h; Heating; | 54% |
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