1103529-64-1

Basic information

• Product Name: phenyl[(thien-2-ylsulfonyl)amino]acetic acid
• Synonyms: phenyl[(thien-2-ylsulfonyl)amino]acetic acid;2-phenyl-2-(2-thienylsulfonylamino)acetic acid;2-phenyl-2-(thiophen-2-ylsulfonylamino)acetic acid;2-phenyl-2-(thiophen-2-ylsulfonylamino)ethanoic acid
• CAS NO: 1103529-64-1
• Molecular Formula: C12H11NO4S2
• Molecular Weight: 297.35004
• Mol File: 1103529-64-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: phenyl[(thien-2-ylsulfonyl)amino]acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl[(thien-2-ylsulfonyl)amino]acetic acid(1103529-64-1)
• EPA Substance Registry System: phenyl[(thien-2-ylsulfonyl)amino]acetic acid(1103529-64-1)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 1103529-64-1(Hazardous Substances Data)

Upstream product

• 6339-87-3 2-thiophensulfonamide 
• 6000-59-5 glyoxalic acid monohydrate 
• 98-80-6 phenylboronic acid 

Relevant articles and documents

Sulfonamides as Amine Component in the Petasis-Borono Mannich Reaction: A Concise Synthesis of α-Aryl- and α-Alkenylglycine Derivatives

A catalyst-free three-component synthesis of α-aryl- and α-alkenylglycine derivatives starting from glyoxylic acid, sulfonamides, and aryl- or alkenylboronic acids is described. This operationally simple method tolerates a broad range of functional groups and enables the generation of a wide array of α-amino acids. Sulfonamides were utilized as amine component in the classic Petasis reaction for the first time.