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CAS 913835-27-5

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B-[4-(1-Methylethyl)-5-pyrimidinyl]boronic acid

Description:
B-[4-(1-Methylethyl)-5-pyrimidinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and other nucleophiles. This compound features a pyrimidine ring substituted with an isopropyl group at the 4-position, contributing to its unique chemical properties. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. Additionally, the presence of the pyrimidine ring may impart biological activity, potentially influencing its interactions with biological targets. The compound is typically used in research settings, particularly in the development of pharmaceuticals and agrochemicals. Its solubility and stability in different solvents can vary, which is important for its application in synthetic procedures. Overall, B-[4-(1-Methylethyl)-5-pyrimidinyl]boronic acid exemplifies the versatility of boronic acids in both synthetic and biological contexts.
Formula:C7H11BN2O2
InChI:InChI=1S/C7H11BN2O2/c1-5(2)7-6(8(11)12)3-9-4-10-7/h3-5,11-12H,1-2H3
InChI key:InChIKey=SMZXLPHORPDPKW-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(C(C)C)=NC=NC1
Synonyms:
  • Boronic acid, [4-(1-methylethyl)-5-pyrimidinyl]-
  • B-[4-(1-Methylethyl)-5-pyrimidinyl]boronic acid
  • Boronic acid, B-[4-(1-methylethyl)-5-pyrimidinyl]-
  • (4-Isopropylpyrimidin-5-yl)boronicacid
  • [4-(Propan-2-yl)pyrimidin-5-yl]boronic acid
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