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CAS 89694-47-3

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B-(4-Chloro-3-methoxyphenyl)boronic acid

Description:
B-(4-Chloro-3-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 a chlorine atom and a methoxy group. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. The presence of the boronic acid group allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. The chlorine and methoxy substituents on the phenyl ring can influence the reactivity and selectivity of the compound in these reactions. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in sensor applications and in the development of drug delivery systems. Overall, B-(4-Chloro-3-methoxyphenyl)boronic acid is a versatile compound with significant utility in synthetic organic chemistry and materials science.
Formula:C7H8BClO3
InChI:InChI=1S/C7H8BClO3/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4,10-11H,1H3
InChI key:InChIKey=DZNNRXURZJLARZ-UHFFFAOYSA-N
SMILES:O(C)C1=CC(B(O)O)=CC=C1Cl
Synonyms:
  • 4-Chloro-3-Methoxyphenylboronic Acid
  • B-(4-Chloro-3-methoxyphenyl)boronic acid
  • Benzeneboronic acid, 4-chloro-3-methoxy-
  • Boronic acid, (4-chloro-3-methoxyphenyl)-
  • boronic acid, B-(4-chloro-3-methoxyphenyl)-
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