93474-57-8

Basic information

• Product Name: 3-hydroxy-2-[(phenylsulfonyl)amino]butanoic acid
• Synonyms: 3-hydroxy-2-[(phenylsulfonyl)amino]butanoic acid
• CAS NO: 93474-57-8
• Molecular Weight: 259.283
• Mol File: 93474-57-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-hydroxy-2-[(phenylsulfonyl)amino]butanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-hydroxy-2-[(phenylsulfonyl)amino]butanoic acid(93474-57-8)
• EPA Substance Registry System: 3-hydroxy-2-[(phenylsulfonyl)amino]butanoic acid(93474-57-8)

Safety Data

• Hazardous Substances Data: 93474-57-8(Hazardous Substances Data)

Upstream product

• 72-19-5 L-threonine 
• 98-09-9 benzenesulfonyl chloride 
• 82659-84-5 methyl cis-L-2-phenyl-5-methyl-2-oxazoline-4-carboxylate 
• 72-19-5 L-threonine 
• 119973-61-4 (2S,3RS)-2-<(phenylsulfonyl)amino>-3-acetoxybutanoic acid 

Downstream Products

• 93474-58-9 (3S,4S)-N-(phenylsulfonyl)-3-amino-4-hydroxy-2-pentanone 
• 120053-28-3 (3S,4S)-3-<(phenylsulfonyl)amino>-4-methyl-2-oxetanone 

Relevant articles and documents

Design, synthesis, molecular docking, antimicrobial, and antioxidant activities of new phenylsulfamoyl carboxylic acids of pharmacological interest

The research explores the facile synthesis of some new phenylsulfamoyl carboxylic acids, their molecular docking, antimicrobial, and antioxidant activities. The procedure involved the mild reaction of amino acids with benzenesulfonyl chloride in a medium

Synthesis and Reactivity of β-Lactones Derived from L-Threonine and Related Amino Acids

The synthesis and nucleophilic ring opening of optically pure N-protected α-amino-β-alkyl β-lactones was investigated.Treatment of N-BOC-L-threonine (8) and N-BOC-L-allo-threonine (9) under modified Mitsunobu conditions (Ph3P, dimethyl azodicarboxylate, -