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CAS 1052686-60-8

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2-Methoxypyrimidine-5-boronic acid pinacol ester

Description:
2-Methoxypyrimidine-5-boronic acid pinacol ester is an organoboron compound characterized by the presence of a pyrimidine ring substituted with a methoxy group and a boronic acid moiety that is esterified with pinacol. This compound typically exhibits properties associated with both boronic acids and pyrimidine derivatives, such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, which are valuable in organic synthesis and medicinal chemistry. The boronic acid functionality allows for the formation of covalent bonds with diols and can participate in Suzuki-Miyaura coupling reactions, making it useful in the synthesis of complex organic molecules. The methoxy group can influence the electronic properties of the pyrimidine ring, potentially affecting its reactivity and interaction with biological targets. Overall, 2-Methoxypyrimidine-5-boronic acid pinacol ester serves as a versatile building block in synthetic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C11H17BN2O3
InChI:InChI=1S/C11H17BN2O3/c1-10(2)11(3,4)17-12(16-10)8-6-13-9(15-5)14-7-8/h6-7H,1-5H3
SMILES:CC1(C)C(C)(C)OB(c2cnc(nc2)OC)O1
Synonyms:
  • 2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine
  • 2-Methoxypyrimidin-5-ylboronic acid pinacol ester
  • 2-Methoxypyrimidine-5-boronic acid pinacol ester
  • Pyrimidine, 2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine ISO 9001：2015 REACH
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