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Oxirane, 2-chloro-2-methyl-, also known as 2-chloro-2-methyloxirane or epichlorohydrin, is a colorless to pale yellow liquid with a molecular formula of C3H5ClO. It is an epoxide compound, which means it contains a three-membered cyclic ether group. Epichlorohydrin is primarily used as a chemical intermediate in the production of various resins, adhesives, and coatings, as well as a stabilizer for rubber and a cross-linking agent for polymers. It is also used in the synthesis of pharmaceuticals and agrochemicals. Due to its reactive nature, it is important to handle epichlorohydrin with care, as it can cause irritation to the eyes, skin, and respiratory system, and may have potential carcinogenic effects.

5950-21-0

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5950-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5950-21-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5950-21:
(6*5)+(5*9)+(4*5)+(3*0)+(2*2)+(1*1)=100
100 % 10 = 0
So 5950-21-0 is a valid CAS Registry Number.

5950-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-2-methyloxirane

1.2 Other means of identification

Product number -
Other names Oxirane,2-chloro-2-methyl

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:5950-21-0 SDS

5950-21-0Relevant academic research and scientific papers

Photoinduced reactions of chloroacetone in solid Ar: Identification of CH2=COClCH3

Tanaka, Nobuaki,Urashima, Yoshitaka,Nishikiori, Hiromasa

, p. 258 - 262 (2015/02/02)

The UV light-induced reactions of chloroacetone in a cryogenic Ar matrix were investigated using infrared spectroscopy. The photoinduced isomerisations of gauche-chloroacetone to syn-chloroacetone and hypochlorous acid 1-methylethenyl ester were confirmed by comparing the experimental and calculated spectra. In addition, the photolysis products were found to be CH2CO and a cyclopropanone-HCl complex. The cyclopropanone-HCl complex was further decomposed into CH2CH2, CO and HCl. The hypochlorous acid 1-methylethenyl ester was further isomerized to 2-chloro-2-methyloxirane.

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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