CAS 1483-56-3: 2-Bromo-5-(trifluoromethyl)benzoic acid
Formula:C8H4BrF3O2
InChI:InChI=1/C8H4BrF3O2/c9-6-2-1-4(8(10,11)12)3-5(6)7(13)14/h1-3H,(H,13,14)
InChI key:InChIKey=REBQGRPKXYIJDC-UHFFFAOYSA-N
SMILES:c1cc(c(cc1C(F)(F)F)C(=O)O)Br
Synonyms:- 6-Bromo-α,α,α-trifluoro-m-toluic acid
- Benzoic Acid, 2-Bromo-5-(Trifluoromethyl)-
- Qvr Be Exfff [Wln]
- m-Toluic acid, 6-bromo-α,α,α-trifluoro-
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Found 4 products.
Benzoic acid, 2-bromo-5-(trifluoromethyl)-
CAS:Formula:C8H4BrF3O2Purity:97%Color and Shape:SolidMolecular weight:269.01542-Bromo-5-(trifluoromethyl)benzoic acid
CAS:2-Bromo-5-(trifluoromethyl)benzoic acid is a reactive electrophile that reacts with butyllithium to form an organolithium compound. The regioselectivity of this reaction depends on the substituent at the bromo position, which can be either para or ortho. 2-Bromo-5-(trifluoromethyl)benzoic acid can be used to selectively convert alkyllithiums into enolates by reacting with them in tetrahydrofuran at room temperature in the presence of 4-dimethylaminopyridine. This reaction is catalyzed by acid or base and stereoselective, giving rise to two possible products from butyllithium: a substituted enolate or an achiral enolate.Formula:C8H4BrF3O2Purity:Min. 95%Molecular weight:269.02 g/mol2-Bromo-5-(trifluoromethyl)benzoic acid
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:269.01699829101562-Bromo-5-(trifluoromethyl)benzoic acid
CAS:2-Bromo-5-(trifluoromethyl)benzoic acidPurity:98+%Color and Shape:SolidMolecular weight:269.02g/mol
