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(2R)-2,3-dihydroxypropyl chloroacetate is a chemical compound characterized by the presence of a chloroacetate group and a 2,3-dihydroxypropyl group. The 2R configuration denotes a specific arrangement of atoms around the 2-carbon atom, which is crucial for its stereochemistry. (2R)-2,3-dihydroxypropyl chloroacetate is known for its potential reactivity in organic synthesis, where the chloroacetate group can participate in nucleophilic substitution or ester hydrolysis, while the 2,3-dihydroxypropyl group, with its two hydroxyl groups, may engage in reactions with aldehydes or ketones. Overall, (2R)-2,3-dihydroxypropyl chloroacetate is a versatile molecule with applications in various areas of organic chemistry and chemical synthesis.

75508-30-4

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75508-30-4 Usage

Uses

Used in Organic Synthesis:
(2R)-2,3-dihydroxypropyl chloroacetate is used as a reagent or building block in organic synthesis for the production of other chemicals. Its unique structure allows for a range of reactions, including nucleophilic substitution and ester hydrolysis, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2R)-2,3-dihydroxypropyl chloroacetate is used as an intermediate in the synthesis of various pharmaceutical compounds. Its stereochemistry and functional groups can be leveraged to create molecules with specific biological activities, contributing to the development of new drugs and therapeutic agents.
Used in Chemical Research:
(2R)-2,3-dihydroxypropyl chloroacetate is utilized in chemical research as a model compound to study the effects of stereochemistry on reactivity and the mechanisms of various organic reactions. Its unique configuration and functional groups provide insights into the behavior of similar compounds in chemical transformations.
Used in Material Science:
In material science, (2R)-2,3-dihydroxypropyl chloroacetate may be employed as a precursor in the synthesis of novel materials with specific properties. Its ability to participate in various chemical reactions can lead to the development of new polymers, coatings, or other materials with tailored characteristics for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 75508-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,0 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75508-30:
(7*7)+(6*5)+(5*5)+(4*0)+(3*8)+(2*3)+(1*0)=134
134 % 10 = 4
So 75508-30-4 is a valid CAS Registry Number.

75508-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydroxypropyl 2-chloroacetate

1.2 Other means of identification

Product number -
Other names Acetic acid,chloro-,2,3-dihydroxypropyl ester

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:75508-30-4 SDS

75508-30-4Downstream Products

75508-30-4Relevant academic research and scientific papers

Anti-trypanosomal compounds. I. In vivo and in vitro activity of inhibitors of glycolysis in trypanosomes

Betbeder, D.,Klaebe, A.,Perie, J. J.,Baltz, T.

, p. 549 - 555 (2007/10/02)

Carboxylated and phosphorylated esters of glycerol, possible inhibitors of the atypical glycolysis in trypanosomes have been synthesised and tested on Trypanosoma equiperdum in vitro and Trypanosoma brucei, on mice, and some of them also on glycerol phosphate dehydrogenase (GDH).Two of these compounds which showed no in vitro activity behaved as good competitive inhibitors of GDH; 3 other compounds were shown to have a good activity on cultures of trypanosomes, but owing to their weak solubility, tests on the enzyme could not be conclusive.Indications for the design of other compounds have been given.

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