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CAS 480425-34-1

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(3-bromo-2-butoxyphenyl)boronic acid

Description:
(3-bromo-2-butoxyphenyl)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 and a butoxy group, which contributes to its hydrophobic properties and influences its reactivity. The boronic acid moiety allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the bromine atom can enhance the electrophilicity of the aromatic system, facilitating further functionalization. This compound may exhibit moderate solubility in organic solvents and can be sensitive to moisture due to the boronic acid group. Its unique structure and functional groups make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in materials science for the development of boron-containing polymers.
Formula:C10H14BBrO3
InChI:InChI=1/C10H14BBrO3/c1-2-3-7-15-10-8(11(13)14)5-4-6-9(10)12/h4-6,13-14H,2-3,7H2,1H3
SMILES:CCCCOc1c(cccc1Br)B(O)O
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