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CAS 480425-35-2

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3-Methoxycarbonylphenylboronic acid pinacol ester

Description:
3-Methoxycarbonylphenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and an ester moiety. This compound typically features a phenyl ring substituted with a methoxycarbonyl group, which enhances its reactivity and solubility in organic solvents. The pinacol ester formation provides stability and can facilitate various synthetic applications, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in organic synthesis for constructing carbon-carbon bonds. The presence of the boron atom allows for the formation of complexes with Lewis bases, making it useful in catalysis and material science. Additionally, the methoxycarbonyl group can serve as a protective group or a handle for further functionalization. Overall, this compound is valuable in the development of pharmaceuticals and advanced materials due to its unique reactivity and structural features. Safety data should be consulted for handling, as organoboron compounds can exhibit varying degrees of toxicity and reactivity.
Formula:C14H19BO4
InChI:InChI=1/C14H19BO4/c1-13(2)14(3,4)19-15(18-13)11-8-6-7-10(9-11)12(16)17-5/h6-9H,1-5H3
SMILES:CC1(C)C(C)(C)OB(c2cccc(c2)C(=O)OC)O1
Synonyms:
  • Methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
  • 3-(Methoxycarbonyl)phenylboronic acid pinacol ester
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