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CAS 2121514-26-7

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B-[3-(Hydroxymethyl)-2-methylphenyl]boronic acid

Description:
B-[3-(Hydroxymethyl)-2-methylphenyl]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. This compound features a phenyl ring substituted with a hydroxymethyl group and a methyl group, contributing to its unique reactivity and solubility properties. The hydroxymethyl group enhances its potential for hydrogen bonding, while the boronic acid moiety allows for applications in organic synthesis, particularly in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. Additionally, boronic acids are often utilized in medicinal chemistry for drug development due to their ability to interact with biological molecules. The compound's solubility in polar solvents and stability under various conditions make it a valuable intermediate in the synthesis of complex organic molecules. Its specific applications may vary, but it is generally recognized for its role in materials science, pharmaceuticals, and as a reagent in organic synthesis.
Formula:C8H11BO3
InChI:InChI=1S/C8H11BO3/c1-6-7(5-10)3-2-4-8(6)9(11)12/h2-4,10-12H,5H2,1H3
InChI key:InChIKey=OQXKXCULNOGPRA-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)C(CO)=CC=C1
Synonyms:
  • B-[3-(Hydroxymethyl)-2-methylphenyl]boronic acid
  • Boronic acid, B-[3-(hydroxymethyl)-2-methylphenyl]-
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