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CAS 1228458-46-5

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B-[4′-(1,1-Dimethylethyl)[1,1′-biphenyl]-2-yl]boronic acid

Description:
B-[4′-(1,1-Dimethylethyl)[1,1′-biphenyl]-2-yl]boronic acid, identified by its CAS number 1228458-46-5, 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 moderate solubility in organic solvents and potential reactivity with various electrophiles due to the boronic acid moiety, which can participate in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. The presence of the bulky tert-butyl group enhances its steric properties, influencing its reactivity and selectivity in chemical reactions. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including drug delivery and sensor technology. Overall, this compound is significant in synthetic organic chemistry and materials science, particularly in the development of pharmaceuticals and advanced materials.
Formula:C16H19BO2
InChI:InChI=1S/C16H19BO2/c1-16(2,3)13-10-8-12(9-11-13)14-6-4-5-7-15(14)17(18)19/h4-11,18-19H,1-3H3
InChI key:InChIKey=MHASLDKIIDDISL-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C=CC=C1)C2=CC=C(C(C)(C)C)C=C2
Synonyms:
  • B-[4′-(1,1-Dimethylethyl)[1,1′-biphenyl]-2-yl]boronic acid
  • Boronic acid, B-[4′-(1,1-dimethylethyl)[1,1′-biphenyl]-2-yl]-
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