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CAS 1451393-04-6

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3-Borono-6-chloro-2-fluorobenzoic acid

Description:
3-Borono-6-chloro-2-fluorobenzoic acid is an organic compound characterized by its boronic acid functional group, which is known for its reactivity in Suzuki coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The presence of a chlorine atom and a fluorine atom on the aromatic ring contributes to its unique electronic properties, influencing its reactivity and solubility. This compound typically appears as a solid at room temperature and is soluble in polar solvents, which is common for carboxylic acids. Its boron atom can form complexes with various ligands, enhancing its utility in medicinal chemistry and materials science. The compound's structure allows for potential applications in drug development and as a building block in the synthesis of more complex molecules. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 3-Borono-6-chloro-2-fluorobenzoic acid is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C7H5BClFO4
InChI:InChI=1S/C7H5BClFO4/c9-4-2-1-3(8(13)14)6(10)5(4)7(11)12/h1-2,13-14H,(H,11,12)
InChI key:InChIKey=QIBCTDACDCASNX-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=C(F)C(B(O)O)=CC=C1Cl
Synonyms:
  • 3-Borono-6-chloro-2-fluorobenzoic acid
  • Benzoic acid, 3-borono-6-chloro-2-fluoro-
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