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CAS 2121514-11-0

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B-[3,5-Dichloro-4-(methoxymethyl)phenyl]boronic acid

Description:
B-[3,5-Dichloro-4-(methoxymethyl)phenyl]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 two chlorine atoms at the 3 and 5 positions and a methoxymethyl group at the 4 position, contributing to its unique reactivity and solubility properties. The presence of the boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This compound may exhibit moderate to high polarity due to the functional groups, influencing its solubility in polar solvents. Additionally, the dichloro substitution can enhance its biological activity and selectivity in pharmaceutical applications. Overall, B-[3,5-Dichloro-4-(methoxymethyl)phenyl]boronic acid is a versatile building block in synthetic chemistry with potential applications in drug development and materials science.
Formula:C8H9BCl2O3
InChI:InChI=1S/C8H9BCl2O3/c1-14-4-6-7(10)2-5(9(12)13)3-8(6)11/h2-3,12-13H,4H2,1H3
InChI key:InChIKey=IYUOVSMFQZZRRE-UHFFFAOYSA-N
SMILES:C(OC)C1=C(Cl)C=C(B(O)O)C=C1Cl
Synonyms:
  • Boronic acid, B-[3,5-dichloro-4-(methoxymethyl)phenyl]-
  • B-[3,5-Dichloro-4-(methoxymethyl)phenyl]boronic acid
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