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Hexanoic acid, 3-amino-2-hydroxy-, (3S)is a chemical compound with the molecular formula C6H13NO3. It is a derivative of hexanoic acid, with an additional amino and hydroxyl group attached to the third carbon of the molecule in the S configuration. Hexanoic acid,3-amino-2-hydroxy-, (3S)is commonly found in nature and is known to have antimicrobial properties. The 3S configuration of the molecule indicates the stereochemistry of the compound, which is important for its biological activity and interactions with other molecules. Overall, hexanoic acid, 3-amino-2-hydroxy-, (3S)is a versatile chemical compound with various potential applications in the pharmaceutical and chemical industries.

402959-32-4

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402959-32-4 Usage

Uses

Used in Pharmaceutical Industry:
Hexanoic acid, 3-amino-2-hydroxy-, (3S)is used as an intermediate in the synthesis of pharmaceuticals for its antimicrobial properties. Its unique structure allows it to be a versatile building block for the development of new drugs.
Used in Chemical Industry:
Hexanoic acid, 3-amino-2-hydroxy-, (3S)is used as a raw material in the synthesis of other organic compounds, taking advantage of its reactive functional groups and stereochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 402959-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,9,5 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 402959-32:
(8*4)+(7*0)+(6*2)+(5*9)+(4*5)+(3*9)+(2*3)+(1*2)=144
144 % 10 = 4
So 402959-32-4 is a valid CAS Registry Number.

402959-32-4SDS

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 (3S)-3-amino-2-hydroxyhexanoic acid

1.2 Other means of identification

Product number -
Other names HEX005

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:402959-32-4 SDS

402959-32-4Relevant academic research and scientific papers

Stereospecific Synthesis of Peptidyl α-Keto Amides as Inhibitors of Calpain

Harbeson, Scott L.,Abelleira, Susan M.,Akiyama, Alan,Barrett, Robert,Carroll, Renee M.,et al.

, p. 2918 - 2929 (1994)

Peptidyl α-keto amides have been synthesized and tested as inhibitors of the cysteine protease calpain.A stereospecific synthesis was devised in which Cbz-dipeptidyl-α-hydroxy amides were oxidized with TEMPO/hypochlorite to the corresponding α-keto amides

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