1-(Trifluoromethyl)acetylbenzotriazole

• Catalog No.: 557447
• CAS Number: 183266-61-7
• M. F.: C8H4F3N3O
• M. W.: 215.1320696
• Purity: 96%

SYNONYMS

• Title: 1-(三氟甲基)乙酰基苯并三唑
• IUPAC name: 1-(1H-1,2,3-benzotriazol-1-yl)-2,2,2-trifluoroethan-1-one
• IUPAC Traditional name: 1-(1,2,3-benzotriazol-1-yl)-2,2,2-trifluoroethanone
• Synonyms: N-Trifluoroacetylbenzotriazole; 1-Benzotriazol-1-yl-2,2,2-trifluoroethanone; 1-苯并三唑-1-基-2,2,2-三氟乙酮; TFABI

DATABASE IDS

• CAS Number: 183266-61-7
• PubChem SID: 24879671
• MDL Number: MFCD00593044

PROPERTIES

• Compostion: mixture of Bt1 and Bt2 isomers
• Empirical Formula (Hill Notation): C8H4F3N3O
• Purity: 96%
• Melting Point: 66-70 °C(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
Application
Reactant for:
• Defluorination dimerization reactions mediated by single electron transfer (SET) reagent, sodium naphthalenide1
• Preparation of scaffolds endowed with anticancer activity against breast cancer cells2
• Synthesis of aspartylglycine dipeptide mimetic3
• Coupling reactions for synthesis of carboxylic acid esters4
• Trifluoroacetylation reactions (Trifluoroacetylating agent)5

Description (简体中文)

包装
1 g in glass bottle
Application
Reactant for:
• Defluorination dimerization reactions mediated by single electron transfer (SET) reagent, sodium naphthalenide1
• Preparation of scaffolds endowed with anticancer activity against breast cancer cells2
• Synthesis of aspartylglycine dipeptide mimetic3
• Coupling reactions for synthesis of carboxylic acid esters4
• Trifluoroacetylation reactions (Trifluoroacetylating agent)5