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21947-76-2

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21947-76-2 Usage

Description

(2R,3R)-2-chloro-3-methyloxirane, also known as (R,R)-(-)-Glycidyl butyrate, is a chiral epoxide with the molecular formula C5H9ClO2. It is characterized by the presence of two asymmetric carbon atoms, resulting in a pair of enantiomers. This chemical compound is widely used in various applications due to its unique properties.

Uses

Used in Organic Synthesis:
(2R,3R)-2-chloro-3-methyloxirane is used as a precursor in the synthesis of various compounds, including pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a diverse range of molecules with potential therapeutic and agricultural benefits.
Used as a Building Block in Chiral Synthesis:
(2R,3R)-2-chloro-3-methyloxirane is utilized as a building block in the synthesis of chiral building blocks. Its chiral nature makes it a valuable component in the development of enantioselective reactions and the production of enantiomerically pure compounds.
Used as a Reagent in Asymmetric Synthesis:
(2R,3R)-2-chloro-3-methyloxirane is employed as a reagent in asymmetric synthesis, where it aids in the selective formation of one enantiomer over another. This selective synthesis is crucial in the production of biologically active compounds with specific pharmacological properties.
Used in Antibacterial and Antitumor Research:
(2R,3R)-2-chloro-3-methyloxirane has been studied for its potential antibacterial and antitumor activities. Its unique structure and reactivity make it a promising candidate for the development of new antimicrobial and anticancer agents.
Used as a Reference Compound in Research and Development:
(2R,3R)-2-chloro-3-methyloxirane is used as a reference compound in the research and development of new compounds. Its well-defined structure and properties make it an ideal standard for comparing the effectiveness and selectivity of newly synthesized compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 21947-76-2 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 21947-76:
(7*2)+(6*1)+(5*9)+(4*4)+(3*7)+(2*7)+(1*6)=122
122 % 10 = 2
So 21947-76-2 is a valid CAS Registry Number.

21947-76-2SDS

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 (2R,3R)-2-chloro-3-methyloxirane

1.2 Other means of identification

Product number -
Other names Propane,1-chloro-1,2-epoxy-,(E)

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:21947-76-2 SDS

21947-76-2Upstream product

21947-76-2Downstream Products

21947-76-2Relevant articles and documents

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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