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2-Hydroxy-3-aminobutanoic acid, also known as L-threo-β-hydroxyaspartic acid or L-β-hydroxyaspartic acid, is a naturally occurring amino acid with the chemical formula C4H9NO4. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is one of the 20 standard amino acids that make up proteins. 2-Hydroxy-3-aminobutanoic acid is characterized by the presence of a hydroxyl group (-OH) at the 2nd carbon and an amino group (-NH2) at the 3rd carbon of the butanoic acid backbone. It plays a significant role in various biological processes, including neurotransmitter synthesis and energy metabolism. Due to its unique structure, 2-hydroxy-3-aminobutanoic acid has potential applications in pharmaceuticals and as a building block for the synthesis of other bioactive compounds.

565-81-1

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565-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 565-81-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 565-81:
(5*5)+(4*6)+(3*5)+(2*8)+(1*1)=81
81 % 10 = 1
So 565-81-1 is a valid CAS Registry Number.

565-81-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-2-hydroxybutanoic acid

1.2 Other means of identification

Product number -
Other names 3-amino-2-hydroxybutyric 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:565-81-1 SDS

565-81-1Downstream Products

565-81-1Relevant academic research and scientific papers

EFFICIENT SYNTHESES OF ENANTIOMERICALLY PURE L AND D-ALLOTHREONINES AND (S) AND (R) ISOSERINES

Pons, Dominique,Savignac, Monique,Genet, Jean-Pierre

, p. 5023 - 5026 (2007/10/02)

Both enantiomers of (S) 1 and (R) 2 isoserine as well (D) 3 and (L) 4 allothreonine are prepared optically pure in three steps by asymmetric Sharpless epoxidation of crotyl and allylic alcohols into 7-10 followed by an improved RuCl3/NaIO4/water oxidation procedure to low molecular weight glycidic acids 11-14 and epoxide opening by ammonia with (20-33 percent) overall yields.

OXIDATIVE DEGRADATION OF β- AND γ-AMINO ACIDS BY CONTACT GLOW DISCHARGE ELECTROLYSIS

Harada, Kaoru,Terasawa, Jun-ichi

, p. 441 - 444 (2007/10/02)

The degradation of β- and γ-amino acids in aqueous solutions by contact glow discharge electrolysis (CGDE) was studied.It was found that the reaction is actually a stepwise oxidative degradation by hydroxyl radical produced by CGDE.

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