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CAS 1627723-05-0

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B-[4-(1-Methylethyl)-3-pyridinyl]boronic acid

Description:
B-[4-(1-Methylethyl)-3-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound features a branched alkyl group, specifically isobutyl, which enhances its lipophilicity and may influence its biological activity. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and materials science. The pyridine ring contributes to the compound's aromaticity and can participate in coordination chemistry. Additionally, boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. The compound's unique structure may also impart specific properties such as solubility in organic solvents and potential interactions with biological targets, making it of interest in drug development and research. Overall, B-[4-(1-Methylethyl)-3-pyridinyl]boronic acid exemplifies the versatility of boron-containing compounds in both synthetic and biological contexts.
Formula:C8H12BNO2
InChI:InChI=1S/C8H12BNO2/c1-6(2)7-3-4-10-5-8(7)9(11)12/h3-6,11-12H,1-2H3
InChI key:InChIKey=LJGCSHWXODMAQM-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(C(C)C)=CC=NC1
Synonyms:
  • Boronic acid, B-[4-(1-methylethyl)-3-pyridinyl]-
  • (4-Isopropylpyridin-3-yl)boronic acid
  • [4-(Propan-2-yl)pyridin-3-yl]boronic acid
  • B-[4-(1-Methylethyl)-3-pyridinyl]boronic acid
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