CAS 848779-86-2
:(3-bromo-2-propoxyphenyl)boronic acid
Description:
(3-Bromo-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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a bromine atom and a propoxy group attached to a phenyl ring, contributing to its unique reactivity and solubility properties. Typically, boronic acids are polar and can exhibit moderate solubility in polar solvents, while the presence of the propoxy group may enhance its solubility in organic solvents. This compound is often utilized in organic synthesis, medicinal chemistry, and materials science due to its ability to act as a versatile building block in the formation of complex molecules. Additionally, the bromine substituent can serve as a leaving group in cross-coupling reactions, further expanding its utility in synthetic applications. Safety data should be consulted, as with all chemical substances, to ensure proper handling and usage.
Formula:C9H12BBrO3
InChI:InChI=1/C9H12BBrO3/c1-2-6-14-9-7(10(12)13)4-3-5-8(9)11/h3-5,12-13H,2,6H2,1H3
SMILES:CCCOc1c(cccc1Br)B(O)O
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Found 3 products.
(3-Bromo-2-propoxyphenyl)boronic acid
CAS:Formula:C9H12BBrO3Purity:95%Color and Shape:SolidMolecular weight:258.90483-Bromo-2-propoxyphenylboronic acid
CAS:<p>3-Bromo-2-propoxyphenylboronic acid</p>Purity:≥95%Molecular weight:258.90g/mol
