CAS 352525-94-1

Boronic acid, B-[3-(aminomethyl)phenyl]-, hydrochloride (1:1)

Description:

Boronic acid, B-[3-(aminomethyl)phenyl]-, hydrochloride (1:1) is a chemical compound characterized by the presence of a boronic acid functional group and an amino group attached to a phenyl ring. This compound typically appears as a white to off-white solid and is soluble in water and various organic solvents, making it versatile for chemical reactions and applications. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, which is particularly useful in organic synthesis and medicinal chemistry. The hydrochloride form indicates that the compound is a salt, enhancing its stability and solubility. This compound may be utilized in the development of pharmaceuticals, particularly in the synthesis of biologically active molecules, and can serve as a building block in the preparation of more complex organic structures. Additionally, its properties make it a candidate for applications in materials science and catalysis. As with many boronic acids, it is important to handle this compound with care, following appropriate safety protocols due to its potential reactivity.

Formula: C₇H₁₁BClNO₂

InChI: InChI=1/C7H10BNO2.ClH/c9-5-6-2-1-3-7(4-6)8(10)11;/h1-4,10-11H,5,9H2;1H

InChI key: InChIKey=NPTBTFRGCBFYPZ-UHFFFAOYSA-N

SMILES: B(O)(O)C1=CC(CN)=CC=C1.Cl

Synonyms:

• (3-Aminomethyl)benzeneboronic acid hydrochloride
• (3-Aminomethylphenyl)boronic acid, hydrochloride
• 3-Aminomethylphenylboronic acid hydrochloride
• 3-Aminomethylphenylboronicacidhydrochloride
• Boronic acid, B-[3-(aminomethyl)phenyl]-, hydrochloride (1:1)
• Boronic acid, [3-(aminomethyl)phenyl]-, hydrochloride
• [3-(Aminomethyl)Phenyl]Boronic Acid Hydrochloride
• [3-(Dihydroxyboranyl)Phenyl]Methanaminium Chloride
• (3-AMINOMETHYLPHENYL)BORONIC ACID HCL
• (3-AMINOETHYLPHENYL)BORONIC ACID HYDROCHLORIDE

3-(Aminomethyl)benzeneboronic acid hydrochloride, 96%

CAS: 352525-94-1

3-(Aminomethyl)benzeneboronic acid hydrochloride is used as intermediates. Hydroxybenzene boronic acids are involved in suzuki miyaura reactions. It is a arylboronic acid. 3-Fluoro-4-hydroxybenzeneboronic acid, can be an effective catalyst for amidation and esterification of carboxylic acids. This

Formula: C₇H₁₀BNO₂•HCl

Purity: 96%

Molecular weight: 187.43

Ref: 02-H53284

(3-(Aminomethyl)phenyl)boronic acid hydrochloride

CAS: 352525-94-1

Formula: C₇H₁₁BClNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 187.43

Ref: 10-F091871

3-Aminomethylphenylboronic acid, HCl

CAS: 352525-94-1

Formula: C₇H₁₁BClNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 187.4317

Ref: IN-DA00BYGJ

3-(Aminomethyl)benzeneboronic acid hydrochloride

CAS: 352525-94-1

3-(Aminomethyl)benzeneboronic acid hydrochloride

Formula: C₇H₁₀BNO₂·ClH

Purity: 99%

Color and Shape: cream solid

Molecular weight: 187.43g/mol

Ref: 54-OR10329

(3-Aminomethylphenyl)boronic acidHydrochloride

CAS: 352525-94-1

(3-Aminomethylphenyl)boronic acidHydrochloride is a boronic acid that has been shown to inhibit glycosylation of proteins. It reversibly binds to the non-reducing end of the N-glycan, and blocks the addition of sugar by inhibiting the enzyme glycogen synthase kinase 3β. This compound has also been shown to inhibit human cell growth, as well as lysates from cells that have been treated with this compound. The nature of this compound is such that it can be used in glycosylation studies on protein or glycopeptide.

Formula: C₇H₁₁BClNO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 187.43 g/mol

Ref: 3D-FA149308