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183266-61-7

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183266-61-7 Structure

183266-61-7 Structure
IdentificationBack Directory
[Name]

1-TRIFLUOROMETHYLACETYLBENZOTRIAZOLE&
[CAS]

183266-61-7
[Synonyms]

TFABI
(Trifluoroacetyl)benzotriazole
N-Trifluoroacetylbenzotriazole
1H-Benzotriazole, 1-(trifluoroacetyl)- (9CI)
1-(Benzotriazol-1-yl)-2,2,2-trifluoroethanone
Ethanone, 1-(1H-benzotriazol-1-yl)-2,2,2-trifluoro-
(Trifluoroacetyl)benzotriazole (1H,2H-isomer mixture)
1-(1H-Benzo[d][1,2,3]triazol-1-yl)-2,2,2-trifluoroethanone
(Trifluoroacetyl)benzotriazole (mixture of 1H- and 2H- isomers)
1-(Trifluoromethyl)acetylbenzotriazole, 96%(mixture of Bt1 and Bt2 isomers)
(Trifluoroacetyl)benzotriazole (mixture of 1H- and 2H- isomers)
[Molecular Formula]

C8H4F3N3O
[MDL Number]

MFCD00593044
[MOL File]

183266-61-7.mol
[Molecular Weight]

215.132
Chemical PropertiesBack Directory
[Melting point ]

66-70 °C(lit.)
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[color ]

White to Almost white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[WGK Germany ]

3
[HS Code ]

2933.99.9701
Hazard InformationBack Directory
[Uses]

Reactant for:
  • Defluorination dimerization reactions mediated by single electron transfer (SET) reagent, sodium naphthalenide
  • Preparation of scaffolds endowed with anticancer activity against breast cancer cells
  • Synthesis of aspartylglycine dipeptide mimetic
  • Coupling reactions for synthesis of carboxylic acid esters
  • Trifluoroacetylation reactions (Trifluoroacetylating agent)
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