131769-28-3

Basic information

• Product Name: 2,2,3,3,4,4,5,5,6,6-Decafluoro-6-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethoxy)-hexanoic acid (2-hydroxy-phenyl)-amide
• Synonyms: 2,2,3,3,4,4,5,5,6,6-Decafluoro-6-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethoxy)-hexanoic acid (2-hydroxy-phenyl)-amide
• CAS NO: 131769-28-3
• Molecular Weight: 571.19
• Mol File: 131769-28-3.mol

Chemical Properties

• CAS DataBase Reference: 2,2,3,3,4,4,5,5,6,6-Decafluoro-6-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethoxy)-hexanoic acid (2-hydroxy-phenyl)-amide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,3,3,4,4,5,5,6,6-Decafluoro-6-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethoxy)-hexanoic acid (2-hydroxy-phenyl)-amide(131769-28-3)
• EPA Substance Registry System: 2,2,3,3,4,4,5,5,6,6-Decafluoro-6-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethoxy)-hexanoic acid (2-hydroxy-phenyl)-amide(131769-28-3)

Safety Data

• Hazardous Substances Data: 131769-28-3(Hazardous Substances Data)

Upstream product

• 25080-18-6 8-trifluoromethyl-7-oxa-perfluorononyliodide 
• 38529-73-6 Chlorosulfuric acid 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-6-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethoxy)-hexyl ester 
• 95-55-6 2-amino-phenol 

Relevant articles and documents

PERFLUOROALKYL AND PERFLUOROALKYLETHER CHLOROSULFATES IN THE SYNTHESIS OF SUBSTITUTED BENZAZOLES

Perfluoroalkyl and perfluoroalkylehter chlorosulfates prepared from correspondign iodides have been utilized in the synthesis of 2-substituted benzoxazoles, benzthiazoles and benzimidazoles.The chlorosulfates react readily with the appropriate 2-hydroxy, 2-mercapto and 2-aminoanilines at or below ambient temperatures.The products are a mixture of the heterocyclic compounds and their precursor anilides except in the case of 2-hydroxyaniline, which gives only the anilide.The initial products obtained are readily converted to the heterocyclic compounds in fair to high yields.