144951-87-1

Basic information

• Product Name: 3-OXA-5-IODOOCTAFLUOROPENTYLSULFONYL AZIDE
• Synonyms: 3-OXA-5-IODOOCTAFLUOROPENTYLSULFONYL AZIDE
• CAS NO: 144951-87-1
• Molecular Formula: C₄F₈IN₃O₃S
• Molecular Weight: 449.012
• Mol File: 144951-87-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-OXA-5-IODOOCTAFLUOROPENTYLSULFONYL AZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-OXA-5-IODOOCTAFLUOROPENTYLSULFONYL AZIDE(144951-87-1)
• EPA Substance Registry System: 3-OXA-5-IODOOCTAFLUOROPENTYLSULFONYL AZIDE(144951-87-1)

Safety Data

• Hazardous Substances Data: 144951-87-1(Hazardous Substances Data)

Upstream product

• 66137-74-4 5-iodooctafluoro-3-oxapentanesulfonyl fluoride 

Downstream Products

• 1314878-66-4 2,2-difluoro-2-(2-iodo-1,1,2,2-tetrafluoroethoxy)acetanilide 
• 148716-83-0 1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-iodoethoxy)-ethanesulfonyl amide 
• 1314878-69-7 3'-trifluoromethyl-2,2-difluoro-2-(2-iodo-1,1,2,2-tetrafluoroethoxy)acetanilide 
• 1314878-75-5 2,2-difluoro-2-(2-iodo-1,1,2,2-tetrafluoroethoxy)-⁽¹⁵⁾N-acetanilide 
• 1314878-78-8 1,1,2,2-tetrafluoro-N-(2-methyl-5-nitrophenyl)-2-(1,1,2,2-tetrafluoro-2-iodoethoxy)ethanesulfonamide 
• 1242102-44-8 N-phenyl-3-(3-oxa-5-iodo-octafluoropentanesulfonamido)pyrrole 
• 754186-41-9 5-ethoxy-5'-iodo-3'-oxa-octafluoropentyl-sulfonyl-1-4,5-dihydro-1H-[1,2,3]triazole 

Relevant articles and documents

Facile and quantitative synthesis of 1,3-diazaheterocycle-fused 1,2,3-triazole derivatives using fluoroalkanesulfonyl azide as a diazo transfer reagent

A series of 1,3-diazaheterocycle-fused 1,2,3-triazoles were conveniently and quantitatively prepared by 1,3-dipolar cycloaddition of heterocyclic ketene aminals with fluoroalkanesulfonyl azide, followed by elimination of fluoroalkanesulfonyl amide at room

Synthesis of fluoroalkanesulfonyl azides and their reactions as fluoroalkanesulfonyl nitrene precursors

Thermolysis or photolysis of the title compounds with cyclohexane, Me2C = CMe2, methyl sulfide and triphenyl phosphine gave the corresponding insertion or addition products via the perfluoroalkanesulfonyl nitrene intermediate.