117632-84-5

Basic information

• Product Name: 1-((trifluoromethyl)sulfonyl)-1H-benzo[d][1,2,3]triazole
• Synonyms: 1-((trifluoromethyl)sulfonyl)-1H-benzo[d][1,2,3]triazole
• CAS NO: 117632-84-5
• Molecular Weight: 251.189
• Mol File: 117632-84-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 36.0 to 40.0 °C
• CAS DataBase Reference: 1-((trifluoromethyl)sulfonyl)-1H-benzo[d][1,2,3]triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((trifluoromethyl)sulfonyl)-1H-benzo[d][1,2,3]triazole(117632-84-5)
• EPA Substance Registry System: 1-((trifluoromethyl)sulfonyl)-1H-benzo[d][1,2,3]triazole(117632-84-5)

Safety Data

• Hazardous Substances Data: 117632-84-5(Hazardous Substances Data)

Usage

Appearance

White to off-white solid

Industrial and research applications

Used in various industrial and research applications

Chemical classification

Sulfonyl azide derivative

Components

Contains a sulfonyl group (SO2) and an azide group (N3)

Potential use

Studied for its potential use in organic synthesis and as a pharmaceutical intermediate

Trifluoromethyl group

Imparts unique properties and reactivity to the compound

Chemical processes

Useful for a range of chemical processes

Safety measures

Should be handled with caution and proper safety measures due to its azide moiety

Upstream product

• 335-05-7 Trifluoromethanesulfonyl fluoride 
• 43183-36-4 1-(trimethylsilyl)-1H-benzotriazole 
• 95-14-7 1,2,3-Benzotriazole 
• 407-25-0 trifluoroacetic anhydride 
• 358-23-6 trifluoromethylsulfonic anhydride 

Downstream Products

• 53984-17-1 (E)-1,1,1-trifluoro-N-(2-styrylphenyl)methanesulfonamide 

Relevant articles and documents

Reactions of 1,2,3-triazoles with trifluoromethanesulfonyl chloride and trifluoromethanesulfonic anhydride

Reactions of 4,5-dibromo-1,2,3-triazole, 1H-1,2,3-benzotriazole, and 2-phenyl-2H-1,2,3-triazole-4-carbonyl chloride with trifluoromethanesulfonyl chloride and trifluoromethanesulfonic anhydride were studied. 4,5-Dibromo-1,2,3-triazole sodium salt reacted

Tert -Butyl nitrite mediated nitrogen transfer reactions: Synthesis of benzotriazoles and azides at room temperature

A conversion of o-phenylenediamines into benzotriazoles was achieved at room temperature using tert-butyl nitrite. The optimized conditions are also well suited for the transformation of sulfonyl and acyl hydrazines into corresponding azides. This protocol does not require any catalyst or acidic medium. The desired products were obtained in excellent yields in a short span of time.