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CAS 70523-24-9

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[2,4-bis(Phenylmethoxy)-5-pyrimidinyl]-boronic acid

Description:
[2,4-bis(Phenylmethoxy)-5-pyrimidinyl]-boronic acid, with the CAS number 70523-24-9, is a boronic acid derivative characterized by its unique structure that includes a pyrimidine ring substituted with two phenylmethoxy groups. 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 biological activity, potentially influencing its interactions with biological targets. Additionally, the compound may exhibit moderate solubility in organic solvents and limited solubility in water, which is common for many organic boron compounds. Its reactivity can be leveraged in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Overall, this compound represents a versatile building block in the synthesis of more complex organic molecules and may have implications in drug development and materials science.
Formula:C18H17BN2O4
InChI:InChI=1/C18H17BN2O4/c22-19(23)16-11-20-18(25-13-15-9-5-2-6-10-15)21-17(16)24-12-14-7-3-1-4-8-14/h1-11,22-23H,12-13H2
SMILES:c1ccc(cc1)COc1c(cnc(n1)OCc1ccccc1)B(O)O
Synonyms:
  • 2,4-Dibenzyluracil-5-boronic acid
  • [2,4-Bis(Benzyloxy)Pyrimidin-5-Yl]Boronic Acid
  • 2,4-Di(benzyloxy)pyrimidine-5-boronic acid
  • 2,4-Bis(Benzyloxy)Pyrimidin-5-Ylboronic Acid
  • 2,4-Bis(benzyloxy)pyrimidine-5-boronic acid
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