| Identification | Back 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 Properties | Back Directory | [Melting point ]
66-70 °C(lit.)
| [solubility ]
soluble in Methanol | [form ]
powder to crystal | [color ]
White to Almost white | [InChI]
1S/C8H4F3N3O/c9-8(10,11)7(15)14-6-4-2-1-3-5(6)12-13-14/h1-4H | [InChIKey]
GVQIQOIKWUOEJP-UHFFFAOYSA-N | [SMILES]
FC(F)(F)C(=O)n1nnc2ccccc12 |
| Hazard Information | Back 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)
| [reaction suitability]
reaction type: C-C Bond Formation |
|
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