Description

(3-(Aminomethyl)phenyl)boronic acid hydrochloride (CAS No. 352525-94-1) is a high-purity boronic acid derivative widely utilized in organic synthesis, pharmaceutical research, and material science. This compound, with the molecular formula C₇H₁₁BClNO₂, features both an aminomethyl group and a boronic acid moiety, making it a versatile building block for Suzuki-Miyaura cross-coupling reactions and other catalytic processes. Its hydrochloride salt form enhances stability and solubility, ensuring reliable performance in aqueous and organic media. Ideal for researchers and scientists, this reagent is rigorously tested for quality and consistency, meeting stringent industry standards. Available in various packaging options to suit laboratory-scale and industrial applications.

Properties

• CAS Number: 352525-94-1
• Complexity: 121
• IUPAC Name: [3-(aminomethyl)phenyl]boronic acid;hydrochloride
• InChI: InChI=1S/C7H10BNO2.ClH/c9-5-6-2-1-3-7(4-6)8(10)11;/h1-4,10-11H,5,9H2;1H
• InChI Key: NPTBTFRGCBFYPZ-UHFFFAOYSA-N
• Exact Mass: 187.0571365
• Molecular Formula: C7H11BClNO2
• Molecular Weight: 187.43
• SMILES: B(C1=CC(=CC=C1)CN)(O)O.Cl
• Topological: 66.5
• Monoisotopic Mass: 187.0571365
• Synonyms: 352525-94-1, (3-(Aminomethyl)phenyl)boronic acid hydrochloride, 3-Aminomethylphenylboronic acid hydrochloride, 3-(Aminomethyl)phenylboronic acid hydrochloride, (3-AMINOMETHYLPHENYL)BORONIC ACID HYDROCHLORIDE, 3-Aminomethylphenylboronic acid, HCl, [3-(aminomethyl)phenyl]boronic acid;hydrochloride, MFCD02093050, [3-(aminomethyl)phenyl]boronic acid hydrochloride, (3-Aminomethylphenyl)boronic acid HCl, (3-aminomethyl)benzeneboronic acid hcl, (3-boronophenyl)methylazanium;chloride, 3-Aminomethylphenylboronic acid HCl, Boronic acid, [3-(aminomethyl)phenyl]-, hydrochloride, SCHEMBL1490536, DTXSID80956692, NPTBTFRGCBFYPZ-UHFFFAOYSA-N, BCP15091, 3-aminomethylphenyl boronic acid HCl, AKOS006228617, AB10727, AS-48236, FA149308, SY020416, DB-007967, DB-015864, CS-0141927, (3-aminomethylphenyl)boronic acidhydrochloride, 3-aminomethyl-phenylboronic acid hydrochloride, 3-aminomethylphenyl boronic acid hydrochloride, (3-(Aminomethyl)phenyl)boronicacidhydrochloride, F20514, (3-aminomethylphenyl)boronic acid, hydrochloride, 3-(aminomethyl)-phenylboronic acid hydrochloride, 3-(Aminomethyl)benzeneboronic acid hydrochloride, (3-(aminomethyl)phenyl) boronic acid hydrochloride, 3-aminomethylphenyl boronic acid hydrochloride salt, 3-aminomethylphenylboronic acid hydrochloride salt, A822678, (3-Aminomethylphenyl)boronic acid hydrochloride, AldrichCPR, [3-(Aminomethyl)phenyl]boronic acid–hydrogen chloride (1/1), 3-(Aminomethyl)benzeneboronic acid hydrochloride (contains varying amounts of Anhydride)

This compound is primarily employed as a key intermediate in the synthesis of bioactive molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient cross-coupling reactions for constructing complex aromatic systems. Researchers also utilize it in the development of sensors and catalysts due to its unique structural properties. The aminomethyl functionality further allows for derivatization, expanding its utility in peptide and polymer chemistry.

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