144951-88-2

Basic information

• Product Name: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE
• Synonyms: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE
• CAS NO: 144951-88-2
• Molecular Formula: C₄HF₈N₃O₃S
• Molecular Weight: 0
• Mol File: 144951-88-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE(144951-88-2)
• EPA Substance Registry System: 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE(144951-88-2)

Safety Data

• Hazardous Substances Data: 144951-88-2(Hazardous Substances Data)

Usage

General Description

1,1,2,2-Tetrafluoro-2-(1,1,2,2-tetrafluoroethoxy)-ethanesulfonyl azide is a chemical compound with the molecular formula C4F8N4O3S. It is a derivative of the sulfonamide class of compounds and is used as a reagent in organic synthesis, particularly in the field of fluorine chemistry and pharmaceutical research. 1,1,2,2-TETRAFLUORO-2-(1,1,2,2-TETRAFLUOROETHOXY)-ETHANESULFONYL AZIDE is known for its ability to introduce fluorine atoms into organic molecules, which can enhance their chemical and biological properties. Additionally, its unique structure and reactivity make it a valuable tool in the development of new materials and pharmaceuticals. However, it is important to handle 1,1,2,2-Tetrafluoro-2-(1,1,2,2-tetrafluoroethoxy)-ethanesulfonyl azide with caution, as it is a potentially hazardous and explosive substance if not handled properly.

Upstream product

• 104729-49-9 5-hydro-3-oxaoctafluoropentanesulfonyl fluoride 

Downstream Products

• 144951-90-6 1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoroethoxy)-ethanesulfonyl amide 
• 845812-06-8 2-(N-methyl-indolinylidene)-(1',1',2',2',4',4',5',5'-octafluoro-3'-oxa-pentyl)-sulfonyl imine 
• 623-73-4 diazoacetic acid ethyl ester 
• 144951-93-9 C₂₂H₁₆F₈NO₃PS 
• 144951-89-3 1,1,2,2-Tetrafluoro-2-(1,1,2,2-tetrafluoro-ethoxy)-ethanesulfonic acid cyclohexylamide 
• 144951-91-7 2,2,3,3-Tetramethyl-1-[1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-ethoxy)-ethanesulfonyl]-aziridine 
• 1314878-73-3 2'-chloro-5'-trifluoromethyl-2,2-difluoro-2-(1,1,2,2-tetrafluoroethoxy)acetanilide 
• 1314878-67-5 2,2-difluoro-2-(1,1,2,2-tetrafluoroethoxy)acetanilide 
• 1314878-84-6 3-(N-(2-(1,1,2,2-tetrafluoroethoxy)-1,1,2 ,2-tetrafluoroethane-1-sulfonamido))-4-methoxybenzaldehyde 
• 1314878-70-0 3'-trifluoromethyl-2,2-difluoro-2-(1,1,2,2-tetrafluoroethoxy)acetanilide 
• 1314878-77-7 1,1,2,2-tetrafluoro-N-(2-methyl-5-nitrophenyl)-2-(1,1,2,2-tetrafluoroethoxy)ethanesulfonamide 
• 1314878-83-5 methyl 3-(2-(1,1,2,2-tetrafluoroethoxy)-1,1,2,2-tetrafluoroethane-1-sulfonamido)benzoate 
• 1304126-53-1 N,N-diisopropyl-N'-[(1,1,2,2,4,4,5,5-octafluoro-3-oxapentyl)sulfonyl]-2-(4-tolyl)acetamidine 

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.