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82079-44-5

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82079-44-5 Usage

Description

(2S)-3-chloro-2-hydroxypropanoic acid, also known as L-3-chloro-2-hydroxypropionic acid, is a chiral chemical compound with the molecular formula C3H5ClO3. It is a derivative of lactic acid, featuring a chlorine atom attached to the second carbon of the hydroxypropionic acid chain. This L-enantiomer is utilized in various industrial applications due to its unique structural properties.

Uses

Used in Pharmaceutical Industry:
(2S)-3-chloro-2-hydroxypropanoic acid serves as a crucial precursor in the synthesis of pharmaceuticals. It is instrumental in producing certain drugs due to its unique molecular structure, which allows for specific interactions with biological targets.
Used in Agrochemical Production:
(2S)-3-chloro-2-hydroxypropanoic acid also finds application as a precursor in the agrochemical industry, contributing to the development of products designed to enhance crop protection and yield.
Used in Organic Synthesis:
(2S)-3-chloro-2-hydroxypropanoic acid is utilized in organic synthesis, where it acts as a building block for the creation of a variety of fine chemicals, highlighting its versatility in chemical reactions.
Used in Food Industry:
With potential applications as a flavoring agent, (2S)-3-chloro-2-hydroxypropanoic acid can be incorporated into the food industry to enhance the taste and aroma of certain products, adding value to the final consumer goods.
Used in Chemical Industry for Material Production:
Furthermore, this compound is employed in the chemical industry for the production of various materials, capitalizing on its chemical properties to create innovative and useful products.

Check Digit Verification of cas no

The CAS Registry Mumber 82079-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,7 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82079-44:
(7*8)+(6*2)+(5*0)+(4*7)+(3*9)+(2*4)+(1*4)=135
135 % 10 = 5
So 82079-44-5 is a valid CAS Registry Number.

82079-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name D-β-Chlorolactic acid

1.2 Other means of identification

Product number -
Other names (2S)-3-chloro-2-hydroxypropanoic acid

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:82079-44-5 SDS

82079-44-5Downstream Products

82079-44-5Relevant articles and documents

D-β-Chlorolactic Acid: A Chemical Synthesis

Morin, Christophe,Sawaya, George

, p. 479 - 480 (1987)

Nitrous deamination of serine-derived β-chloroalanine proceeds without significant racemization, thus opening a chemical route to optically active β-chlorolactic acid.

Novel chemo-enzymatic synthesis of optically active platelet activating factor

Kumar,Bhakuni

, p. 3463 - 3466 (2007/10/02)

This paper describes an enantioselective enzymatic synthesis of biologically active platelet activating factor (PAF) starting from chloropyruvic acid.

Enzymatic Synthesis of Optically Pure (R)-(-)-Mandelic Acid and Other 2-Hydroxycarboxylic Acids: Screening for the Enzyme, and Its Purification, Characterization and Use

Yamazaki, Yoshimitsu,Maeda, Hidekatsu

, p. 2621 - 2632 (2007/10/02)

An enzyme that reduces benzoylformate with NADH to form (R)-mandelate was extracted from cells of Streptococcus faecalis IFO 12964 and purified to more than 95percent purity as evidenced by gel electrophoresis.Physicochemical and enzymic properties were studied.From the substrate specificity, we concluded that the enzyme was a kind of (R)-2-hydroxyisocaproate dehydrogenase.Optically pure (R)-(-)-mandelic acid was prepared with the enzyme, NADH, and alcohol, formate or glucose dehydrogenase in 84 ca. 93percent yield.Five (R)-2-hydroxyalkanoic acids (C4 - C6) or their Ba salts, (R)-(+)-3-phenyllactic acid and (S)-(-)-3-chlorolactic acid were also prepared with the enzyme.

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