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Cyclopentyl chloroformate

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Company Name: Changzhou Fullone Chemical Co., Ltd.
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Products Intro: Product Name:cyclopentyl chloroformate
CAS:50715-28-1
Purity:98% Package:1KG;5KG;25KG
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Products Intro: Product Name:Cyclopentyl chloroformate
CAS:50715-28-1
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Henan Tianfu Chemical Co.,Ltd.
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Products Intro: Product Name:Cyclopentyl Chloroformate
CAS:50715-28-1
Purity:99% Package:25KG;5KG;1KG
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Products Intro: Product Name:Cyclopentyl chloroformate
CAS:50715-28-1
Purity:99% Package:1kg;1USD
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Products Intro: Product Name:Cyclopentyl Chloroformate
CAS:50715-28-1
Purity:>95% Package:1g;5g;25g;100g

Cyclopentyl chloroformate manufacturers

Cyclopentyl chloroformate Basic information
Product Name:Cyclopentyl chloroformate
Synonyms:CYCLOPENTYL CHLOROFORMATE;CARBONOCHLORIDIC ACID, CYCLOPENTYL ESTER;Cyclopentyl carbonochloridoate;Cyclopentyl carbonochloridate;Cyclopentyl carbonochloridoate, [(Chlorocarbonyl)oxy]cyclopentane, [(Chloroformyl)oxy]cyclopentane;yclopentyl chloroformate
CAS:50715-28-1
MF:C6H9ClO2
MW:148.59
EINECS:411-460-0
Product Categories:CHLOROFORMATES;Ring Systems
Mol File:50715-28-1.mol
Cyclopentyl chloroformate Structure
Cyclopentyl chloroformate Chemical Properties
Boiling point 69.0-70.5 °C(Press: 25 Torr)
density 1.19±0.1 g/cm3(Predicted)
form liquid
color Brown
InChIInChI=1S/C6H9ClO2/c7-6(8)9-5-3-1-2-4-5/h5H,1-4H2
InChIKeyZFQCRLNKHHXELH-UHFFFAOYSA-N
SMILESC(Cl)(OC1CCCC1)=O
CAS DataBase Reference50715-28-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,T
Risk Statements 10-22-23-41-43-48/22
Safety Statements 26-36/37/39-45
RIDADR UN3277
Hazard Note Irritant
HazardClass 6.1, 8
HS Code 2916200090
MSDS Information
Cyclopentyl chloroformate Usage And Synthesis
UsesCyclopentyl Chloroformate is a chemical reagent used in the synthesis of novel peptidomimetic Hep C protease inhibitors.
Synthesis
Triphosgene

32315-10-9

Cyclopentanol

96-41-3

Cyclopentyl chloroformate

50715-28-1

A mixed solution of cyclopentanol (10.9 mL, 120 mmol) and pyridine (10.7 mL, 132 mmol) was added slowly and dropwise to a solution of triphosgene (11.87 g, 40.0 mmol) in anhydrous ether (100 mL) at -70 °C. The reaction mixture was stirred continuously for 1 h at this temperature and then removed from the low temperature bath. Stirring was continued at room temperature for 1.5 h. Subsequently, 1.0 N HCl aqueous solution (110 mL) was added for acidification. The organic phase was separated, washed with brine (60 mL) and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to afford cyclopentyl chloroformate (14.395 g, boiling point 80 °C/75 mmHg, 80.7% yield). The resulting cyclopentyl chloroformate could be used directly in the subsequent reaction without further purification.

References[1] Patent: CN106045802, 2016, A. Location in patent: Paragraph 0044-0045
[2] Patent: WO2008/95058, 2008, A1. Location in patent: Page/Page column 31
[3] European Journal of Medicinal Chemistry, 1993, vol. 28, # 1, p. 37 - 45
[4] Patent: WO2008/38175, 2008, A2. Location in patent: Page/Page column 38
[5] Patent: CN107417748, 2017, A. Location in patent: Paragraph 0106
Cyclopentyl chloroformate Preparation Products And Raw materials
Raw materialsCyclopentylamine-->Cyclopentanol-->Diethyl ether-->Triphosgene-->Water-->Diphosgene-->Hydrochloric acid-->PHOSGENE
Preparation ProductsCyclopentyl chloride
Tag:Cyclopentyl chloroformate(50715-28-1) Related Product Information
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