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(2S)-2-propylbutanedioic acid, also known as (S)-2-propylsuccinic acid, is a chiral chemical compound with the molecular formula C7H12O4. It possesses two enantiomers, with the (2S) form representing the specific stereochemistry of (2S)-2-propylbutanedioic acid. This acid is characterized by its potential anti-inflammatory and anti-oxidant properties, which contribute to its significance in both the chemical and medical fields.

688-05-1

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688-05-1 Usage

Uses

Used in Pharmaceutical Synthesis:
(2S)-2-propylbutanedioic acid is utilized as a key building block in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Compounds Synthesis:
(2S)-2-propylbutanedioic acid also serves as a fundamental building block for the synthesis of other organic compounds, contributing to the advancement of organic chemistry and the creation of novel molecules with diverse applications.
Used in Medical Applications:
(2S)-2-propylbutanedioic acid is studied for its potential medical applications due to its anti-inflammatory and anti-oxidant properties. These characteristics suggest that it may be beneficial in the treatment of conditions associated with inflammation and oxidative stress, although further research is required to fully understand its therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 688-05-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 688-05:
(5*6)+(4*8)+(3*8)+(2*0)+(1*5)=91
91 % 10 = 1
So 688-05-1 is a valid CAS Registry Number.

688-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-Propylsuccinic acid

1.2 Other means of identification

Product number -
Other names -

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:688-05-1 SDS

688-05-1Upstream product

688-05-1Downstream Products

688-05-1Relevant academic research and scientific papers

Chemoenzymatic synthesis of glutamic acid analogues: Substrate specificity and synthetic applications of branched chain aminotransferase from Escherichia coli

Xian, Mo,Alaux, Sebastien,Sagot, Emmanuelle,Gefflaut, Thierry

, p. 7560 - 7566 (2007)

(Chemical Equation Presented) A new route to α-keto acids is described, based on the ozonolysis of enol acetates obtained from α-substituted β-keto esters. Escherichia coli branched chain aminotransferase (BCAT) activity toward a variety of substituted 2-oxoglutaric acids was demonstrated analytically. BCAT was shown to have a broad substrate spectrum, complementary to that of aspartate aminotransferase, and to offer access to a variety of glutamic acid analogues. The usefulness of BCAT was demonstrated through the synthesis of several 3- and 4-substituted derivatives.

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