DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
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inquiryWelcome 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
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inquiryProduct Description Product Name 1-Chlorobutane CAS No. 109-69-3 Appearance Colorless transparent liquid Assay ≥99.5% Capacity 2000mt/year Min.packing 500gram
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inquiryCompany Name: Hefei TNJ Chemical Industry Co.,Ltd. Registered Address: B911 Xincheng Business Center,South of Dongliu Road, Zhengwu District, Hefei, Anhui,China Register Capital:¥12,000,000.00 Re-Register Date:2009.09.03 Register Numbe
Cas:109-69-3
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inquiryhigh quality Appearance:Colorless liquid 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
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
1-Chlorobutane Product name: 1-Chlorobutane CAS No.: 109-69-3 Molecular formula C4H9Cl Molecular weight: 92.57 Structural formula:
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
TIANFUCHEM--109-69-3--1-Chlorobutane 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 relation
Cas:109-69-3
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inquiryChemical Name: n-butylchloride CAS No.:109-69-3 Molecular Fomula: C4H9Cl Chemical Structure: Molecular weight: 92.57 Appearance: clear liquid Assay:99.0% min Appearance: Colorless Transparent Liquid Storage: Preserve in well-closed, li
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
Cas:109-69-3
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inquiryCompany information: Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in carbomer,carbopol,lead acetate,meglumine diphenyl ethylamine and other chemical raw materials and chemical reagents research and development production ente
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inquiry1-Chlorobutane CAS:109-69-3 Specification Product Name 1-Chlorobutane CAS No. 109-69-3 Appearance Colorless transparent liquid Assay ≥99.5% Capacity 2000mt/year Min.
Appearance:white or light yellow crystalline powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:By
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
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inquiryJ&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
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
109-69-3 1-Chlorobutane Appearance:liquid Storage:room temperature Package:according to customers' requirements Application:Pharma intermediates Transportation:By air(EMS or EUB or FedEx or TNT ect...) or by sea(FOB or CIF or CNF ect...)or accordi
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
Cas:109-69-3
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inquiryProduct name: 1-Chlorobutane CAS No.:109-69-3 Molecule Formula:C4H9Cl Molecule Weight:92.57 Purity: 99.0% Package: 200kg/drum Description:Colorless liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
Cas:109-69-3
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inquiryProduct 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,
Cas:109-69-3
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inquiryWe are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
Cas:109-69-3
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inquirySuperior quality, moderate price & quick delivery. Appearance:Colorless liquid Storage:sealed in a cool place Package:25kg/drum, or as per your request. Application:Medicine, pesticide, organic synthesis intermediates Transportation:as per your
ISO/factory/goodqualityAppearance:off white Storage:Dry,cool place Package:drum Application:active pharmaceutical ingredients Transportation:by air/sea/express Port:shenzhen/shanghai
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
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
Best service,high quality and cheap price. Storage:Keep away from heat,sparks and flames. Package:25kg/50kg/200kg drum or Customer demand Application:Used as pharmaceutical intermediates Transportation:BY sea/air or by courier
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
Cas:109-69-3
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inquiryOur clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Organic synthesis. Preparation of butyl cellulose butylating agent. Solvent. Application:Organic synthesis. Preparation of butyl cellulose butylating agent. Solvent.
Conditions | Yield |
---|---|
With hydrogenchloride; water; oxygen; copper dichloride at 59.9℃; Product distribution; Mechanism; other alcohols, var. conc. of reagents, var. temperat.; | A 100% B n/a |
With phosphan; chlorine Rate constant; Thermodynamic data; Ea, ΔS(excit.); also in the presence of pyridine; |
Conditions | Yield |
---|---|
With hexabutylguanidinium chloride at 100℃; for 0.05h; | 100% |
Conditions | Yield |
---|---|
With phosphorus pentachloride; trichlorophosphate for 0.5h; Heating; other alkyl and aryl iodides; | 98% |
With mercury dichloride |
Conditions | Yield |
---|---|
With hydrogenchloride In water at 115℃; for 2h; Reagent/catalyst; Temperature; | 96.9% |
With hydrogenchloride; dimethyl sulfoxide In water at 85 - 95℃; for 20h; Temperature; Reagent/catalyst; | 93.5% |
With hydrogenchloride at 75 - 80℃; Concentration; | 91.5% |
Conditions | Yield |
---|---|
With hydrogenchloride; tetrabutylphosphonium ion; silica gel at 170℃; under 760 Torr; | A 95% B 4 % Chromat. |
Conditions | Yield |
---|---|
With Trichloromethanesulfonyl chloride In dichloromethane at 18℃; for 3.5h; Irradiation; | A n/a B 95% C n/a |
dichlorofluoromethanesulphenyl chloride
n-butane
A
n-Butyl chloride
B
bis(dichlorofluoromethyl)disulfane
C
2-(Dichloro-fluoro-methylsulfanyl)-butane
Conditions | Yield |
---|---|
A 8.5% B 92.4% C 2.3% | |
A 8.5% B 92.4% C 2.3% |
1,1-dibutoxy-2,2-dichloro-ethene
A
n-Butyl chloride
B
butoxycarbonyldichloromethanesulfenyl chloride
Conditions | Yield |
---|---|
With sulfur monochloride In dichloromethane under Ar atmosphere, spontaneous heating to 45 deg C 30 min, 20 deg C 2,5 h; | A n/a B 90% |
butan-1-ol
A
phosphoric acid tributyl ester
B
n-Butyl chloride
C
dibutyl ether
Conditions | Yield |
---|---|
With oxygen; phosphan; copper(l) chloride; copper dichloride at 24.9℃; Kinetics; Product distribution; Mechanism; ΔE(excit.), ΔS(excit.); other reagents, other catalysts; | A 90% B n/a C n/a |
With oxygen; phosphan; copper(l) chloride; copper dichloride at 24.9℃; | A 90% B n/a C n/a |
tetrachloromethane
dibutylmercury
B
n-Butyl chloride
C
chloroform
D
n-butylmercuric chloride
Conditions | Yield |
---|---|
In neat (no solvent) 150°C, 25 h; further products; | A 2% B 87% C 105 % D 7% E 89% |
Dibutylboran-butylester
phosphorus pentachloride
A
n-Butyl chloride
B
dibutylchloroborane
C
trichlorophosphate
Conditions | Yield |
---|---|
exothermic react.; removing C4H9Cl and OPCl3 at reduced pressure, distn. of residue; | A n/a B 89% C n/a |
1-bromo-butane
1-bromo-3-chloro-2-methyl propane
A
n-Butyl chloride
B
1,3-dibromo-2-methylpropane
Conditions | Yield |
---|---|
With tetrabutylammomium bromide at 105 - 110℃; Inert atmosphere; Schlenk technique; | A n/a B 86% |
Conditions | Yield |
---|---|
With zinc(II) chloride at 125℃; for 1h; Product distribution; Rate constant; other time; the thermal stability of the product was investigated by DTA, DTG and TG; | A n/a B 85% |
Conditions | Yield |
---|---|
With chlorine In tetrahydrofuran at 0℃; Product distribution; | A 14% B 84% |
With chlorine In diethyl ether at 0℃; | A 84 % Chromat. B 14 % Chromat. |
phosphorus pentachloride
1,4-bis(di-n-butoxy)-boryl-phenylene
A
n-Butyl chloride
B
1,4-bis(dichloroboryl)benzene
C
trichlorophosphate
Conditions | Yield |
---|---|
In tetrachloromethane boiled for 7 h using back-flow; distn. of CCl4, sublimation; | A n/a B 84% C n/a |
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate; tert-butylmagnesium chloride In tetrahydrofuran at 0℃; for 1.5h; Inert atmosphere; | 83% |
With borohydride exchange resin; nickel diacetate In methanol for 3h; Ambient temperature; | 95 % Chromat. |
With Amberlite IRA-400; borohydride form; copper(II) sulfate In methanol at 20℃; for 1h; Reduction; | 95 % Chromat. |
Conditions | Yield |
---|---|
With calcium chloride at 122℃; for 1h; Product distribution; other time; | A n/a B 81% |
With calcium chloride at 122℃; for 1h; | A n/a B 81% |
Conditions | Yield |
---|---|
With sulfur dichloride In dichloromethane | A n/a B 81% |
Conditions | Yield |
---|---|
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine In toluene Reflux; | 81% |
N,N-dimethyl-formamide
butan-1-ol
A
n-Butyl chloride
B
n-butyl formate
Conditions | Yield |
---|---|
With benzoyl chloride at 80℃; for 2h; | A 81% B n/a |
phosgene
vinylphosphonic acid-di-n-butyl ester
A
n-Butyl chloride
B
vinyldichlorophosphine oxide
Conditions | Yield |
---|---|
A n/a B 80.5% |
chlorodifluoromethansulfenylchloride
n-butane
A
s-butyl chloride
B
n-Butyl chloride
C
2-(Chloro-difluoro-methylsulfanyl)-butane
D
n-C4H9SCF2Cl
E
bis(chlorodifluoromethyl)disulfane
Conditions | Yield |
---|---|
A 21.8% B 2.8% C 12.7% D 7% E 80.3% | |
A 21.8% B 2.8% C 12.7% D 7% E 80.3% |
Conditions | Yield |
---|---|
With Cl*2H2O In toluene at 150℃; | 80% |
With chloride ions In gas at 125℃; under 640 Torr; Rate constant; nitrogen buffer gas; | |
With chloride at 30.9℃; under 760 Torr; Kinetics; Thermodynamic data; Equilibrium constant; ΔE0, ΔG0, mechanism; | |
With chloride In gas at 35 - 150℃; under 640 Torr; Thermodynamic data; Ea; var. pressure; | |
With 1,1,2,2-tetrachloroethylene at 90℃; for 24h; Inert atmosphere; |
phosphorus pentachloride
1,3-bis(di-n-butoxy)-boryl-phenylene
A
n-Butyl chloride
B
1,3-(BCl2)2-C6H4
C
trichlorophosphate
Conditions | Yield |
---|---|
In tetrachloromethane boiled for 7 h using back-flow; distn.; | A n/a B 79% C n/a |
Conditions | Yield |
---|---|
With hydrogenchloride; aluminium trichloride; silica gel at 170℃; under 760 Torr; Product distribution; other catalysts, other alcohols, other products; | A 7 % Chromat. B 78% C n/a |
Conditions | Yield |
---|---|
With CPT | A n/a B 77% |
Butyl phosphorodifluoridite
ethyl chloromethyl ether
A
n-Butyl chloride
B
(ethoxymethyl)phosphonic difluoride
Conditions | Yield |
---|---|
With iron(III) chloride for 1.5h; Heating; | A n/a B 76% |
trichloromethylphosphonous dichloride
butan-1-ol
A
dibutyl hydrogen phosphite
B
n-Butyl chloride
C
chloroform
Conditions | Yield |
---|---|
A 75.4% B n/a C n/a |
methyl 2,2-dichloro-2-methoxyacetate
Butyl phosphorodifluoridite
A
n-Butyl chloride
B
phosphonic difluoride
Conditions | Yield |
---|---|
With iron(III) chloride at 60 - 80℃; for 0.75h; | A n/a B 75% |
Conditions | Yield |
---|---|
With 1-n-butyl-3-(methoxyethoxymethyl)imidazolium chloride at 90℃; for 3h; Solvent; Inert atmosphere; Green chemistry; | 100% |
With tetrabutyl ammonium fluoride at 80℃; for 12h; | 70% |
durch Erhitzen molekularer Mengen auf dem Wasserbad; |
Conditions | Yield |
---|---|
With 3-(2-ethoxy-2-oxoethyl)-1-methyl-1H-imidazol-3-ium chloride at 90℃; for 3h; Inert atmosphere; Green chemistry; | 100% |
Conditions | Yield |
---|---|
With 3-(2-ethoxy-2-oxoethyl)-1-methyl-1H-imidazol-3-ium chloride at 90℃; for 3h; Inert atmosphere; Green chemistry; | 100% |
Conditions | Yield |
---|---|
With hydrogen; sodium hydrogencarbonate; {W(CO)5Cl}(1-) In tetrahydrofuran at 150℃; under 80 - 85 Torr; for 24h; | 100% |
n-Butyl chloride
(E)-N-(phenylmethylene)-1-(trimethylsilyl)methylamine
dimethylfumarate
(3R,4R)-2-Phenyl-pyrrolidine-3,4-dicarboxylic acid dimethyl ester
Conditions | Yield |
---|---|
In N,N,N,N,N,N-hexamethylphosphoric triamide at 40 - 45℃; | 100% |
1-methyl-1H-imidazole
n-Butyl chloride
1-butyl-3-methylimidazolium chloride
Conditions | Yield |
---|---|
Alkylation; | 100% |
In toluene at 112 - 113℃; for 3h; | 100% |
at 170℃; Microwave irradiation; | 99% |
n-Butyl chloride
tert-butyl 2-phenyldiazene-1-carboxylate
Conditions | Yield |
---|---|
Stage #1: n-Butyl chloride With zinc(II) chloride In tetrahydrofuran Stage #2: tert-butyl 2-phenyldiazene-1-carboxylate In tetrahydrofuran at -80℃; | 100% |
Conditions | Yield |
---|---|
for 5h; Heating; | 100% |
In acetonitrile at 75℃; for 24h; Inert atmosphere; | 99% |
at 50℃; for 24h; Inert atmosphere; | 87% |
In acetonitrile for 96h; Reflux; | 56% |
n-Butyl chloride
1-isopropyllimidazole
1-butyl-3-isopropylimidazolium chloride
Conditions | Yield |
---|---|
at 75℃; for 12h; Inert atmosphere; neat (no solvent); | 100% |
n-Butyl chloride
[1',1',1'-d3]-1-methyl-1H-imidazole
[1”,1”,1”-d3]-1-n-butyl-3-methylimidazolium chloride
Conditions | Yield |
---|---|
at 95℃; | 100% |
Conditions | Yield |
---|---|
With C11H19N2O2(1+)*Cl(1-) at 90℃; for 3h; Inert atmosphere; Green chemistry; | 100% |
With tetrabutylammomium bromide; sodium hydroxide In water at 100℃; for 2h; | 93 %Chromat. |
Conditions | Yield |
---|---|
With C11H19N2O2(1+)*Cl(1-) at 90℃; for 3h; Inert atmosphere; Green chemistry; | 100% |
tin
n-Butyl chloride
A
dibutyltin chloride
B
tributyltin chloride
Conditions | Yield |
---|---|
With catalyst: dicyclohexyl-18-crown-6/n-C4H9I In N,N-dimethyl-formamide 120°C; 24 h; excess KI;; analyzed by GLC;; | A 99% B 1% |
With catalyst: dibenzo-18-crown-6/n-C4H9I In N,N-dimethyl-formamide 120°C; 24 h; excess KI;; analyzed by GLC;; | A 98% B 2% |
With catalyst: dibenzo-18-crown-6/n-C8H17I In N,N-dimethyl-formamide 120°C; 24 h; excess KI;; analyzed by GLC;; | A 98% B 2% |
n-Butyl chloride
(-)-(2S)-(nonafluorobutane-1-sulfonyloxy)-propionic acid tert-butyl ester
(+)-(2S)-methyl-hexanoic acid tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: n-Butyl chloride With magnesium Inert atmosphere; Stage #2: (-)-(2S)-(nonafluorobutane-1-sulfonyloxy)-propionic acid tert-butyl ester With zinc(II) chloride at 0℃; for 3h; Inert atmosphere; optical yield given as %ee; enantiospecific reaction; | 99% |
n-Butyl chloride
(-)-(2S)-trifluoromethanesulfonyloxy-3-methyl-butyric acid tert-butyl ester
(+)-(2R)-isopropyl-hexanoic acid tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: n-Butyl chloride With magnesium In tetrahydrofuran Inert atmosphere; Stage #2: (-)-(2S)-trifluoromethanesulfonyloxy-3-methyl-butyric acid tert-butyl ester With zinc(II) chloride In tetrahydrofuran at 0℃; for 3h; Inert atmosphere; optical yield given as %ee; enantiospecific reaction; | 99% |
n-Butyl chloride
(-)-(2S)-trifluoromethanesulfonyloxy-(3S)-methyl-pentanoic acid tert-butyl ester
(+)-(2R)-[propyl-(1'S)-methyl]-hexanoic acid tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: n-Butyl chloride With magnesium Inert atmosphere; Stage #2: (-)-(2S)-trifluoromethanesulfonyloxy-(3S)-methyl-pentanoic acid tert-butyl ester With zinc(II) chloride at 0℃; for 3h; Inert atmosphere; optical yield given as %ee; enantiospecific reaction; | 99% |
n-Butyl chloride
(-)-(2S)-trifluoromethanesulfonyloxy-propionic acid tert-butyl ester
(+)-(2S)-methyl-hexanoic acid tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: n-Butyl chloride With magnesium In tetrahydrofuran Inert atmosphere; Stage #2: (-)-(2S)-trifluoromethanesulfonyloxy-propionic acid tert-butyl ester With zinc(II) chloride In tetrahydrofuran at 0℃; for 3h; Inert atmosphere; optical yield given as %ee; enantiospecific reaction; | 99% |
Conditions | Yield |
---|---|
In ethanol at 90℃; for 24h; Sealed tube; | 99% |
1-(3-bromophenyl)-1H-imidazole
n-Butyl chloride
Conditions | Yield |
---|---|
In acetonitrile at 120℃; for 16h; Sealed tube; | 99% |
n-Butyl chloride
Conditions | Yield |
---|---|
With triethylamine at 25℃; for 16h; | 99% |
Conditions | Yield |
---|---|
With triethylamine at 25℃; for 16h; | 99% |
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane | 99% |
With tetrabutylammomium bromide; sodium hydroxide In water at 20 - 60℃; for 1h; |
n-Butyl chloride
1-butyl-3-methylimidazolium chloride
Conditions | Yield |
---|---|
With 1-methyl-1H-imidazole | 98% |
Conditions | Yield |
---|---|
With magnesium In diethyl ether; toluene at 50 - 60℃; Solvent; Inert atmosphere; Flow reactor; | 98% |
With sodium In Petroleum ether (Ar); vigorous stirred suspn. of Na was maintained at 115°C for 30 min, then one drop of SnCl4 was added and ClC4H9 was added dropwise within 3 h at 0-5°C, after 75 min stirring SnCl4 was dropped into mixt. at the same temp. within 2 h; after stirring for a further 2 h at 20-25°C mixt. was filtered off and residue treated with tBuOH, solvents were distd. off from filtrate; identification by GC after methylation; | 91% |
With magnesium In 2-methyltetrahydrofuran for 5h; Solvent; Reflux; | 77.87% |
Stage #1: n-Butyl chloride With magnesium for 0.5h; Reflux; Stage #2: tin(IV) chloride for 3h; Reflux; |
Conditions | Yield |
---|---|
Stage #1: n-Butyl chloride With magnesium; lithium chloride In diethyl ether at 35℃; for 12h; Stage #2: With sodium methylate; zinc(II) chloride In diethyl ether at 0℃; Inert atmosphere; Stage #3: benzaldehyde With (S)-N-(3-methyl-1-(1-pyrrolidin-1-yl)butan-2-yl)-P,P-di(naphthalen-1-yl)phosphinic amideamine at 20℃; for 2h; Neat (no solvent); optical yield given as %ee; | 98% |
Stage #1: n-Butyl chloride With magnesium In diethyl ether Inert atmosphere; Stage #2: benzaldehyde With titanium(IV) isopropylate; (Sa)-2'-[(R)-hydroxy(phenyl)methyl]-(1,1'-binaphthalen)-2-ol In toluene at -40℃; for 4.16h; Grignard reaction; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 41% |
n-Butyl chloride
Conditions | Yield |
---|---|
In acetonitrile at 120℃; for 16h; Sealed tube; | 98% |
In acetonitrile at 150℃; for 24h; | 98% |
1,6-Hexanediamine
n-Butyl chloride
tetraethylammonium bicarbonate
1,6-bis-(n-butoxycarbonyl-amino)-hexane
Conditions | Yield |
---|---|
Stage #1: 1,6-Hexanediamine; tetraethylammonium bicarbonate In acetonitrile at 20℃; for 1h; Stage #2: n-Butyl chloride In acetonitrile at 80℃; for 3h; | 98% |
Stage #1: 1,6-Hexanediamine; tetraethylammonium bicarbonate In acetonitrile at 20℃; for 2h; Green chemistry; Stage #2: n-Butyl chloride In acetonitrile at 80℃; for 3h; Green chemistry; | 90% |
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