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1955-68-6

1955-68-6 Structure

1955-68-6 Structure
IdentificationBack Directory
[Name]

L-ASPARTIC ACID BETA-HYDROXAMATE
[CAS]

1955-68-6
[Synonyms]

HDX
AAH
Nsc141662
N4-Hydroxy-L-asparagine
L-Asparagine, N-hydroxy-
L-ASPARTICACIDβ-HYDROXAMATE
L-Aspartyl-?-hydroxamic acid
l-aspartic acid β-hydroxamate
3-(Hydroxycarbamoyl)-L-alanine
L-ASPARTIC ACID BETA-HYDROXAMATE
L-ASPARTYL-ALPHA-HYDROXAMIC ACID
L-ASPARTIC ACID BETA-HYDROXAMATE powder
L-aspartic acid B-hydroxamate*crystalline
L-ASPARTIC ACID BETA-HYDROXAMATE USP/EP/BP
(S)-3-Amino-3-carboxypropanehydroximic acid
(S)-2-aMino-4-(hydroxyaMino)-4-oxobutanoic acid
(S)-2-Amino-4-hydroxy-4-(hydroxyimino)butanoic acid
L-Aspartic acid β-hydroxaMate serine raceMase inhibitor
L-Aspartic acid beta-hydroxamate serine racemase inhibitor
[Molecular Formula]

C4H8N2O4
[MDL Number]

MFCD00050389
[MOL File]

1955-68-6.mol
[Molecular Weight]

148.12
Chemical PropertiesBack Directory
[Melting point ]

171-172 °C
[density ]

1.532±0.06 g/cm3(Predicted)
[storage temp. ]

−20°C
[pka]

3.02±0.10(Predicted)
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

Hydroxylated lecithin, also known as b-L-aspartylhydroxamate or b-aspartohydroxamic acid, belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. Based on a literature review a small amount of articles have been published on Hydroxylated lecithin.
[Uses]

L-ASPARTIC ACID BETA-HYDROXAMATE can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical and pharmaceutical production process.
[Definition]

ChEBI: Beta-L-aspartylhydroxamic acid is a non-proteinogenic L-alpha-amino acid that is L-asparagine hydroxylated at N-4. It is a hydroxamic acid, a L-asparagine derivative and a non-proteinogenic L-alpha-amino acid. It is a tautomer of a beta-L-aspartylhydroxamic acid zwitterion.
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