CAS 868272-84-8
:(3-bromo-5-fluoro-2-propoxyphenyl)boronic acid
Description:
(3-Bromo-5-fluoro-2-propoxyphenyl)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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom at the 3-position, a fluorine atom at the 5-position, and a propoxy group at the 2-position, contributing to its unique reactivity and solubility properties. The presence of both halogen substituents (bromine and fluorine) can influence the electronic properties of the molecule, potentially enhancing its reactivity in cross-coupling reactions. Additionally, the boronic acid group allows for participation in Suzuki-Miyaura coupling reactions, which are pivotal in forming carbon-carbon bonds. Overall, this compound's structural features make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in materials science.
Formula:C9H11BBrFO3
InChI:InChI=1/C9H11BBrFO3/c1-2-3-15-9-7(10(13)14)4-6(12)5-8(9)11/h4-5,13-14H,2-3H2,1H3
SMILES:CCCOc1c(cc(cc1Br)F)B(O)O
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Found 3 products.
(3-Bromo-5-fluoro-2-propoxyphenyl)boronic acid
CAS:Formula:C9H11BBrFO3Purity:95%Color and Shape:SolidMolecular weight:276.89523-Bromo-5-fluoro-2-propoxyphenylboronic acid
CAS:3-Bromo-5-fluoro-2-propoxyphenylboronic acidPurity:95%Molecular weight:276.90g/mol
