477867-80-4

Basic information

• Product Name: 2-[(2-([4-(4-CHLOROPHENYL)-1,3-THIAZOL-2-YL]AMINO)-2-OXOETHYL)SULFANYL]ACETIC ACID
• Synonyms: 2-[(2-([4-(4-CHLOROPHENYL)-1,3-THIAZOL-2-YL]AMINO)-2-OXOETHYL)SULFANYL]ACETIC ACID
• CAS NO: 477867-80-4
• Molecular Formula: C₁₃H₁₁ClN₂O₃S₂
• Molecular Weight: 342.82
• Mol File: 477867-80-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[(2-([4-(4-CHLOROPHENYL)-1,3-THIAZOL-2-YL]AMINO)-2-OXOETHYL)SULFANYL]ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2-([4-(4-CHLOROPHENYL)-1,3-THIAZOL-2-YL]AMINO)-2-OXOETHYL)SULFANYL]ACETIC ACID(477867-80-4)
• EPA Substance Registry System: 2-[(2-([4-(4-CHLOROPHENYL)-1,3-THIAZOL-2-YL]AMINO)-2-OXOETHYL)SULFANYL]ACETIC ACID(477867-80-4)

Safety Data

• Hazardous Substances Data: 477867-80-4(Hazardous Substances Data)

Upstream product

• 2103-99-3 4-(4-chlorophenyl)-2-thiazolamine 
• 99-91-2 para-chloroacetophenone 
• 6125-31-1 2-chloro-N-[4-(4-chlorophenyl)-1,3-thiazol-2-yl]acetamide 
• 68-11-1 mercaptoacetic acid 

Relevant articles and documents

Synthesis and antioxidant activities of acetamidomethylsulfonyl bis heterocycles-oxazolyl/thiazolyl/imidazolyl-1,3,4-Oxadiazoles

A new class of acetamidomethylsulfonyl bis heterocycles-oxazolyl-1,3,4- oxadiazoles, -thiazolyl-1,3,4-oxadiazoles, and -imidazolyl-1,3,4-oxadiazoles were synthesized from the synthetic intermediates, methyl 2-((4-aryloxazol-2- ylcarbamoyl)methylsulfonyl)acetate, methyl 2-((4-arylthiazol-2-ylcarbamoyl) methylsulfonyl)acetate, and methyl 2-((4-aryl-1H-imidazol-2-ylcarbamoyl) methylsulfonyl)acetate. All the title compounds were tested for their antioxidant activity. The oxadiazolylmethylsulfonyloxazolylacetamide displayed excellent radical-scavenging activity when compared with the standard ascorbic acid. A new class of acetamidomethylsulfonyl bis heterocycles-oxazolyl/ thiazolyl/imidazolyl-1,3,4-oxadiazoles were synthesized and tested for their antioxidant activity. The oxadiazolylmethylsulfonyloxazolylacetamide displayed excellent radical-scavenging activity when compared with the standard ascorbic acid.