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(R)-3-CHLOROLACTIC ACID, with the chemical formula C3H5ClO3, is an optically active organic acid that possesses the unique ability to rotate plane-polarized light. The incorporation of a chlorine atom in its structure endows it with distinctive properties, making it a valuable compound in various applications. It is predominantly utilized as a chiral building block in the synthesis of pharmaceuticals and agrochemicals, and also serves as a resolving agent for the separation of racemic mixtures, which are mixtures of equal amounts of two enantiomers (mirror-image isomers) of a compound. (R)-3-CHLOROLACTIC ACID is thus a significant player in the realm of organic synthesis, with a wide array of applications across different industries.

61505-41-7

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61505-41-7 Usage

Uses

Used in Pharmaceutical Industry:
(R)-3-CHLOROLACTIC ACID is used as a chiral building block for the synthesis of various pharmaceuticals, leveraging its optical activity to create enantiomerically pure compounds. This is crucial in drug development, as different enantiomers can exhibit distinct biological activities and pharmacological effects.
Used in Agrochemical Industry:
In the agrochemical sector, (R)-3-CHLOROLACTIC ACID serves a similar role as a chiral building block, enabling the production of enantiomerically pure agrochemicals. This ensures targeted effects on pests or weeds while minimizing potential side effects on non-target organisms and the environment.
Used in Chiral Synthesis:
(R)-3-CHLOROLACTIC ACID is used as a resolving agent in chiral synthesis for the separation of racemic mixtures. This application is vital for obtaining pure enantiomers, which is essential in various chemical and biological processes where the stereochemistry of a molecule significantly influences its properties and interactions.
Used in Organic Synthesis:
Beyond its applications in specific industries, (R)-3-CHLOROLACTIC ACID is a versatile compound in organic synthesis, where its unique properties can be harnessed for the creation of a diverse range of organic compounds with potential applications in materials science, chemical research, and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 61505-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,0 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61505-41:
(7*6)+(6*1)+(5*5)+(4*0)+(3*5)+(2*4)+(1*1)=97
97 % 10 = 7
So 61505-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H5ClO3/c4-1-2(5)3(6)7/h2,5H,1H2,(H,6,7)/t2-/m0/s1

61505-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3-chloro-2-hydroxypropanoic acid

1.2 Other means of identification

Product number -
Other names L-b-Chlorolactic 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:61505-41-7 SDS

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