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CAS 153035-56-4

:

B-(4′-Propyl[1,1′-biphenyl]-4-yl)boronic acid

Description:
B-(4′-Propyl[1,1′-biphenyl]-4-yl)boronic acid, with the CAS number 153035-56-4, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a biphenyl structure. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with solubility in polar organic solvents like methanol and ethanol. It is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the synthesis of complex organic molecules. The presence of the propyl group enhances its solubility and reactivity, making it a valuable intermediate in the development of pharmaceuticals and organic materials. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including sensors and drug delivery systems. Overall, this compound is significant in both academic research and industrial applications due to its versatile reactivity and functional properties.
Formula:C15H17BO2
InChI:InChI=1S/C15H17BO2/c1-2-3-12-4-6-13(7-5-12)14-8-10-15(11-9-14)16(17)18/h4-11,17-18H,2-3H2,1H3
InChI key:InChIKey=NOQFUISBLHCDSR-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(C=C1)C2=CC=C(CCC)C=C2
Synonyms:
  • (4′-Propyl-1,1′-biphenyl-4-yl)boronic acid
  • B-(4′-Propyl[1,1′-biphenyl]-4-yl)boronic acid
  • Boronic acid, (4′-propyl[1,1′-biphenyl]-4-yl)-
  • Boronic acid, B-(4′-propyl[1,1′-biphenyl]-4-yl)-
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