3-(trifluoromethyl)benzoyl Chloride

CAS : 2251-65-2

Ref. 3D-FT105442

Informations sur le produit

• Nom: 3-(trifluoromethyl)benzoyl Chloride
• Synonymes: 3-(Trifluoromethyl)-Benzoylchlorid, 3-(Trifluoromethyl)Benzoy, 3-(Trifluoromethyl)Benzoyl Chloride, 3-(Trifluoromethyl)benzoylchloride, 3-Trifluoromethylbenzoyl Chloride, 3-[Trifluoromethyl]phenylcarbonyl chloride, 5-[4-(trifluoromethyl)phenyl]-2H-tetrazole, Alpha,Alpha,Alpha-Trifluoro-M-Toluoy, Alpha,Alpha,Alpha-Trifluoro-M-Tolyl Chloride, Benzoyl chloride, 3-(trifluoromethyl)-, M-Trifluoromethylbenzoyl Chloride, Mtf-Boc, NSC 88307, Timtec-Bb Sbb006693, Trifluoromethylbenzoyl Chloride, m-(Trifluoromethyl)benzoyl chloride, m-Toluoyl chloride, alpha,alpha,alpha-trifluoro-, m-Toluoyl chloride, α,α,α-trifluoro-, α,α,α-Trifluoro-m-toluoyl chloride, à,à,à-trifluoro-m-toluoyl chloride

Description

3-(Trifluoromethyl)benzoyl chloride is an organic compound that reacts with ammonium nitrate to produce diphenyl sulfoxide. This reaction is catalyzed by chloroformate and the product of this reaction is then hydrolyzed by hydrogen bond to yield 3-(trifluoromethyl)benzoic acid. The 3-chlorobenzoyl chloride can be converted into a variety of compounds through different reactions, such as conversion to chloroformates, xanthates, silver trifluoromethanesulfonate, or b-raf inhibitors.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 208.56 g/mol
• Formule: C₈H₄ClF₃O
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C8H4ClF3O/c9-7(13)5-2-1-3-6(4-5)8(10,11)12/h1-4H
• Code InChI: InChIKey=RUJYJCANMOTJMO-UHFFFAOYSA-N
• SMILES: O=C(Cl)c1cccc(C(F)(F)F)c1