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CAS 75705-21-4

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4-Aminomethylphenylboronic acid hydrochloride

Description:
4-Aminomethylphenylboronic acid hydrochloride is an organic compound characterized by the presence of both an amine and a boronic acid functional group. It typically appears as a white to off-white crystalline solid, which is soluble in water and polar organic solvents. The compound features a phenyl ring substituted with an aminomethyl group and a boronic acid moiety, which makes it useful in various applications, particularly in medicinal chemistry and organic synthesis. The boronic acid group allows for reversible covalent bonding with diols, making it valuable in the development of drug delivery systems and in the synthesis of complex organic molecules. Additionally, the hydrochloride salt form enhances its stability and solubility in aqueous environments. This compound is often utilized in the synthesis of biologically active molecules and as a reagent in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in forming carbon-carbon bonds in organic synthesis. Safety precautions should be observed when handling this compound, as with many boron-containing compounds, due to potential irritant properties.
Formula:C7H10BNO2
InChI:InChI=1/C7H10BNO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,10-11H,5,9H2
SMILES:c1cc(ccc1CN)B(O)O
Synonyms:
  • [4-(Aminomethyl)Phenyl]Boronic Acid
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