54836-96-3

Basic information

• Product Name: α-Amino-2-carboxy-1-azetidinebutanoic acid
• Synonyms: α-Amino-2-carboxy-1-azetidinebutanoic acid
• CAS NO: 54836-96-3
• Molecular Formula: C8H14N2O4
• Molecular Weight: 202.20776
• Mol File: 54836-96-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: α-Amino-2-carboxy-1-azetidinebutanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: α-Amino-2-carboxy-1-azetidinebutanoic acid(54836-96-3)
• EPA Substance Registry System: α-Amino-2-carboxy-1-azetidinebutanoic acid(54836-96-3)

Safety Data

• Hazardous Substances Data: 54836-96-3(Hazardous Substances Data)

Upstream product

• 78553-61-4 (S)-1-((S)-3-Amino-3-ethoxycarbonyl-propyl)-azetidine-2-carboxylic acid methyl ester; hydrochloride 
• 78553-56-7 (S)-1-((S)-3-Amino-3-methoxycarbonyl-propyl)-azetidine-2-carboxylic acid methyl ester; hydrochloride 
• 111705-75-0 ethyl (2R,αS)-2-ethoxycarbonyl-α-trifluoroacetylamino-1-azetidinebutanoate 
• 2133-34-8 (2S)-azetidine-2-carboxylic acid 
• 7729-30-8 (R)-azetidine-2-carboxylic acid 
• 187796-28-7 tert-butyl (S)-1-[(S)-3-(tert-butoxycarbonylamino)-4-tert-butoxy-4-oxobutyl]azetidine-2-carboxylate 
• 201283-51-4 (S)-1-((S)-3-tert-Butoxycarbonyl-3-tert-butoxycarbonylamino-propionyl)-azetidine-2-carboxylic acid tert-butyl ester 
• 201283-52-5 (S)-1-((S)-3-tert-Butoxycarbonyl-3-tert-butoxycarbonylamino-thiopropionyl)-azetidine-2-carboxylic acid tert-butyl ester 
• 78553-50-1 (S)-1-((S)-3-Benzyloxycarbonylamino-3-methoxycarbonyl-propyl)-azetidine-2-carboxylic acid methyl ester 
• 78553-55-6 (S)-1-((S)-3-Benzyloxycarbonylamino-3-ethoxycarbonyl-propyl)-azetidine-2-carboxylic acid methyl ester 

Relevant articles and documents

SYNTHESIS AND BIOLOGICAL ACTIVITY OF (+)-NICOTIANAMINE

(+)-Nicotianamine and its naturally occurring antipode exhibited the same biological activity with regard to chlorophyll formation of chlorotic leaflets of the mutant chloronerva.It is therefore concluded that nicotianamine does not exert its functions by a stereospecific binding to a macromolecular surface. - Key Word Index: Lycopersicon esculentum; tomato mutant chloronerva; Solanaceae; (2R:3'R:3''R)-N--azetidine-2-carboxylic acid; (2R:3'R)-N-(3-amino-3-carboxypropyl)-azetidine-2-carboxylic acid; chlorophyll formation.

Optimierung der Synthese von Nicotianamin aus L-Azetidin-2-carbonsaeure

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SYNTHESIS OF NICOTIANAMINE AND A RELATED COMPOUND, DERIVATIVES OF AZETIDINE-2-CARBOXYLIC ACID

The synthesis of nicotianamine (1) and a related compound (2) - amino acid derivatives having the azetidine ring - was achieved by reductive coupling of L-aspartic-β-semialdehyde derivatives with L-azetidine-2-carboxylic acid methyl ester.