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CAS 850567-49-6

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(2-Amino-4-methoxycarbonylphenyl)boronic acid pinacol ester hydrochloride

Description:
(2-Amino-4-methoxycarbonylphenyl)boronic acid pinacol ester hydrochloride, with the CAS number 850567-49-6, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that contains an amino group and a methoxycarbonyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols and other Lewis bases, making it useful in various organic synthesis applications, particularly in Suzuki-Miyaura cross-coupling reactions. The hydrochloride form indicates the presence of a hydrochloric acid moiety, which can enhance solubility in polar solvents. The pinacol ester group contributes to the stability and reactivity of the boronic acid, allowing for selective reactions in synthetic pathways. Overall, this compound is valuable in medicinal chemistry and materials science due to its functional groups that facilitate diverse chemical transformations.
Formula:C14H21BClNO4
InChI:InChI=1/C14H20BNO4.ClH/c1-13(2)14(3,4)20-15(19-13)10-7-6-9(8-11(10)16)12(17)18-5;/h6-8H,16H2,1-5H3;1H
SMILES:CC1(C)C(C)(C)OB(c2ccc(cc2N)C(=O)OC)O1.Cl
Synonyms:
  • 2-Amino-4-(methoxycarbonyl)benzeneboronic acid pinacol ester hydrochloride
  • Methyl 3-Amino-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Benzoate Hydrochloride
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