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CAS 1217500-86-1

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B-[2-(Phenylmethoxy)-5-pyrimidinyl]boronic acid

Description:
B-[2-(Phenylmethoxy)-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 a phenylmethoxy group, contributing to its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The boronic acid moiety is significant for its role in various chemical reactions, including Suzuki coupling, which is widely used in organic synthesis to form carbon-carbon bonds. Additionally, the compound may exhibit properties such as solubility in polar solvents and stability under certain conditions, making it suitable for various synthetic applications. Its unique structure allows for interactions with biological targets, which may be explored in drug discovery and development. Overall, B-[2-(Phenylmethoxy)-5-pyrimidinyl]boronic acid represents a versatile building block in organic synthesis and medicinal chemistry.
Formula:C11H11BN2O3
InChI:InChI=1S/C11H11BN2O3/c15-12(16)10-6-13-11(14-7-10)17-8-9-4-2-1-3-5-9/h1-7,15-16H,8H2
InChI key:InChIKey=CYHDQODLSLRGRH-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C=2N=CC(B(O)O)=CN2
Synonyms:
  • [2-(Benzyloxy)pyrimidin-5-yl]boronic acid
  • (2-(Benzyloxy)pyrimidin-5-yl)boronic acid
  • Boronic acid, B-[2-(phenylmethoxy)-5-pyrimidinyl]-
  • B-[2-(Phenylmethoxy)-5-pyrimidinyl]boronic acid
  • 2-Benzyloxypyrimidine-5-boronic acid
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