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CAS 501944-42-9

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5-Fluorobenzothiophene-2-boronic acid

Description:
5-Fluorobenzothiophene-2-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzothiophene ring that is substituted with a fluorine atom. This compound typically exhibits properties associated with both boronic acids and heterocyclic aromatic compounds. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The fluorine substitution can influence the electronic properties of the molecule, potentially enhancing its reactivity and solubility in organic solvents. Additionally, the presence of the thiophene ring contributes to the compound's aromaticity and stability. Overall, 5-Fluorobenzothiophene-2-boronic acid is of interest in the development of pharmaceuticals and agrochemicals, particularly in the context of drug discovery and material science, due to its unique structural features and reactivity.
Formula:C8H6BFO2S
InChI:InChI=1/C8H6BFO2S/c10-6-1-2-7-5(3-6)4-8(13-7)9(11)12/h1-4,11-12H
SMILES:c1cc2c(cc1F)cc(B(O)O)s2
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