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CAS 156635-90-4

:

B-[4-[(4-Methoxyphenyl)methoxy]phenyl]boronic acid

Description:
B-[4-[(4-Methoxyphenyl)methoxy]phenyl]boronic acid, with the CAS number 156635-90-4, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a biphenyl structure. This compound features a methoxy group on one of the phenyl rings, which enhances its solubility and reactivity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis, medicinal chemistry, and materials science. The presence of the methoxy substituent can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions in chemical reactions. Additionally, boronic acids are often utilized in Suzuki coupling reactions, which are important for the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Overall, B-[4-[(4-Methoxyphenyl)methoxy]phenyl]boronic acid is a versatile compound with significant implications in both research and industrial applications.
Formula:C14H15BO4
InChI:InChI=1/C13H13BO3/c15-14(16)12-7-4-8-13(9-12)17-10-11-5-2-1-3-6-11/h1-9,15-16H,10H2
InChI key:InChIKey=UCYGEGISTWJFFA-UHFFFAOYSA-N
SMILES:O(CC1=CC=C(OC)C=C1)C2=CC=C(B(O)O)C=C2
Synonyms:
  • (4-((4-Methoxybenzyl)oxy)phenyl)boronic acid
  • 3-(Benzyloxy)-benzeneboronic acid
  • 3-Benzyloxyphenylboronic acid
  • B-[4-[(4-Methoxyphenyl)methoxy]phenyl]boronic acid
  • Boronic acid, B-[4-[(4-methoxyphenyl)methoxy]phenyl]-
  • Boronic acid, [4-[(4-methoxyphenyl)methoxy]phenyl]-
  • [4-[(4-Methoxyphenyl)methoxy]phenyl]boronic acid
  • 4-(4'-METHOXYBENZYLOXY)PHENYLBORONIC ACID
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