CAS 1309980-96-8

B-[2-Bromo-3-(trifluoromethoxy)phenyl]boronic acid

Description:

B-[2-Bromo-3-(trifluoromethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis and medicinal chemistry. The compound features a bromine atom and a trifluoromethoxy group attached to a phenyl ring, contributing to its unique reactivity and potential applications in cross-coupling reactions, such as Suzuki-Miyaura coupling. The trifluoromethoxy group enhances the compound's electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, the presence of the boronic acid moiety allows for the formation of stable complexes with various substrates, facilitating its use in the development of sensors and catalysts. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry, particularly in the context of functionalized aromatic compounds.

Formula: C₇H₅BBrF₃O₃

InChI: InChI=1S/C7H5BBrF3O3/c9-6-4(8(13)14)2-1-3-5(6)15-7(10,11)12/h1-3,13-14H

InChI key: InChIKey=RIXLLVIGWOPVSW-UHFFFAOYSA-N

SMILES: O(C(F)(F)F)C1=C(Br)C(B(O)O)=CC=C1

Synonyms:

• Boronic acid, B-[2-bromo-3-(trifluoromethoxy)phenyl]-
• B-[2-Bromo-3-(trifluoromethoxy)phenyl]boronic acid

Boronic acid, B-[2-bromo-3-(trifluoromethoxy)phenyl]-

CAS: 1309980-96-8

Formula: C₇H₅BBrF₃O₃

Molecular weight: 284.8230

Ref: IN-DA01RGXR