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CAS 134896-34-7

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2-PROPOXYPHENYLBORONIC ACID

Description:
2-Propyoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a propoxy group. This compound typically exhibits properties such as being a white to off-white solid, soluble in organic solvents, and having moderate stability under standard conditions. The boronic acid moiety allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. It can participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. Additionally, the presence of the propoxy group can influence its solubility and reactivity, enhancing its utility in drug development and material science. Safety data indicates that, like many organoboron compounds, it should be handled with care due to potential irritant properties. Overall, 2-propyoxyphenylboronic acid is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C9H13BO3
InChI:InChI=1/C9H13BO3/c1-2-7-13-9-6-4-3-5-8(9)10(11)12/h3-6,11-12H,2,7H2,1H3
SMILES:CCCOc1ccccc1B(O)O
Synonyms:
  • Akos Brn-0175
  • 2-(N-Propoxy)Benzeneboronic Acid
  • Boronic acid, B-(2-propoxyphenyl)-
  • 1-Borono-2-propoxybenzene, 2-Boronophenyl propyl ether
  • 2-Propoxybenzeneboronic acid
  • 2-Propoxyphenylboronicaci
  • 2-PROPOXYPHENYLBORONIC ACID
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