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CAS 175883-61-1

:

B-(3,5-Dichloro-4-methoxyphenyl)boronic acid

Description:
B-(3,5-Dichloro-4-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both chlorine and methoxy groups. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents. The presence of the boronic acid moiety allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, which are essential in organic synthesis for forming carbon-carbon bonds. The dichloro and methoxy substituents on the phenyl ring can influence the compound's reactivity and solubility, as well as its electronic properties. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be utilized in various applications, including drug delivery and sensor technology. Overall, B-(3,5-Dichloro-4-methoxyphenyl)boronic acid is a versatile compound with significant utility in synthetic organic chemistry and materials science.
Formula:C7H7BCl2O3
InChI:InChI=1/C7H7BCl2O3/c1-13-7-5(9)2-4(8(11)12)3-6(7)10/h2-3,11-12H,1H3
InChI key:InChIKey=JHCLSOGJYUVJNQ-UHFFFAOYSA-N
SMILES:O(C)C1=C(Cl)C=C(B(O)O)C=C1Cl
Synonyms:
  • 3,5-Dichloro-4-methoxyphenylboronic acid
  • B-(3,5-Dichloro-4-methoxyphenyl)boronic acid
  • Boronic acid, (3,5-dichloro-4-methoxyphenyl)-
  • boronic acid, B-(3,5-dichloro-4-methoxyphenyl)-
  • (3,5-Dichloro-4-methoxyphenyl)boronic acid
  • (3,5-dichloro-4-methoxyphenyl)boronicaci
  • AKOS BRN-0059
  • 4-Borono-2,6-dichloroanisole
  • 3,5-DICHLORO-4-METHOXYBENZENEBORONIC ACID
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