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CAS 89641-18-9

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(2,4-Dimethoxy-5-pyrimidinyl)-boronic acid

Description:
(2,4-Dimethoxy-5-pyrimidinyl)-boronic acid, with the CAS number 89641-18-9, is a boronic acid derivative characterized by the presence of a pyrimidine ring substituted with two methoxy groups at the 2 and 4 positions, and a boronic acid functional group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the pyrimidine moiety may impart specific biological activities, potentially making it relevant in drug discovery. Additionally, the methoxy groups can influence the compound's solubility and reactivity. Generally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. The compound's stability, reactivity, and solubility can vary based on environmental conditions such as pH and temperature, which are important considerations in its practical applications.
Formula:C6H9BN2O4
InChI:InChI=1/C6H9BN2O4/c1-12-5-4(7(10)11)3-8-6(9-5)13-2/h3,10-11H,1-2H3
SMILES:COc1c(cnc(n1)OC)B(O)O
Synonyms:
  • 2,4-Dimethoxypyrimidine-5-boronic acid
  • 2,4-Dimethoxyprimidine-5-boronic acid
  • (2,4-Dimethoxypyrimidin-5-Yl)Boronic Acid
  • 2,4-Dimethoxypryimidine-5-Boronic Acid
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