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1-chloro-1,2-epoxypropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21947-75-1

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21947-75-1 Usage

Synonyms

chloropropylene oxide

Physical state

colorless liquid

Reactivity

highly reactive

Uses

a. Building block in the synthesis of organic compounds
b. Glycerol derivatives
c. Surfactants
d. Solvent
e. Intermediate in pharmaceuticals, pesticides, and industrial chemicals production

Hazardous properties

potential carcinogen

Health hazards

a. Eye irritation
b. Skin irritation
c. Respiratory system irritation

Safety measures

handle with caution and use appropriate safety measures

Check Digit Verification of cas no

The CAS Registry Mumber 21947-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21947-75:
(7*2)+(6*1)+(5*9)+(4*4)+(3*7)+(2*7)+(1*5)=121
121 % 10 = 1
So 21947-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H5ClO/c1-2-3(4)5-2/h2-3H,1H3/t2-,3-/m0/s1

21947-75-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-1-chloro-1,2-epoxypropane

1.2 Other means of identification

Product number -
Other names OXIRANE,2-CHLORO-3-METHYL-, CIS-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21947-75-1 SDS

21947-75-1Upstream product

21947-75-1Relevant academic research and scientific papers

Radical Reactions of Epoxides. Chlorine Atom Abstraction from α- and β-Chloro Epoxides by the Triphenyltin Radical

Krosley, Kevin W.,Gleicher, Gerald Jay,Clapp Gary E.

, p. 840 - 844 (2007/10/02)

The four isomers of chloroepoxypropane have been prepared, and their relative reactivities with triphenyltin haydride have been determined.The three α-chloroepoxypropanes react at a much slower rate than does epichlorohydrin, the only β-chloro epoxide of the four.The nature of the increased reactivity for the β-chloro epoxides has been investigated by studying two pair of diastereomeric β-chloro epoxides, and a single acyclic β-chloro ether.The results are discussed in terms of the inductive, and stereoelectronic effects of the epoxide.

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