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CAS 871125-75-6

:

B-[3-[(3-Methoxyphenyl)methoxy]phenyl]boronic acid

Description:
B-[3-[(3-Methoxyphenyl)methoxy]phenyl]boronic acid, with the CAS number 871125-75-6, 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 boron atom bonded to a phenyl ring that is further substituted with a methoxy group, enhancing its solubility and reactivity. The methoxyphenyl substituents contribute to its electronic properties, making it useful in various applications, including organic synthesis and medicinal chemistry. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, this compound may exhibit properties such as moderate stability under ambient conditions and potential reactivity with biological molecules, making it of interest in drug development and materials science. Its specific characteristics, such as melting point, solubility, and reactivity, would typically be determined through experimental methods.
Formula:C14H15BO4
InChI:InChI=1S/C14H15BO4/c1-18-13-6-2-4-11(8-13)10-19-14-7-3-5-12(9-14)15(16)17/h2-9,16-17H,10H2,1H3
InChI key:InChIKey=BLIXUNCSDKZOOX-UHFFFAOYSA-N
SMILES:O(CC1=CC(OC)=CC=C1)C2=CC(B(O)O)=CC=C2
Synonyms:
  • [3-(3-Methoxybenzyloxy)phenyl]boronic acid
  • B-[3-[(3-Methoxyphenyl)methoxy]phenyl]boronic acid
  • Boronic acid, [3-[(3-methoxyphenyl)methoxy]phenyl]-
  • [3-[(3-Methoxyphenyl)methoxy]phenyl]boronic acid
  • Boronic acid, B-[3-[(3-methoxyphenyl)methoxy]phenyl]-
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