CAS 13209-38-6

2-AMINOBENZHYDROL

Description:

2-Aminobenzhydrol, also known as 2-aminodiphenylmethanol, is an organic compound characterized by the presence of both an amino group and a hydroxyl group attached to a biphenyl structure. It typically appears as a white to off-white solid and is soluble in organic solvents while having limited solubility in water. The compound exhibits properties typical of both amines and alcohols, making it a versatile intermediate in organic synthesis. It can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, due to the reactivity of its functional groups. Additionally, 2-aminobenzhydrol may exhibit biological activity, which has led to its investigation in pharmaceutical applications. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks upon exposure. Overall, 2-aminobenzhydrol is a significant compound in both industrial and research settings, valued for its chemical reactivity and potential applications.

Formula: C₁₃H₁₃NO

InChI: InChI=1/C13H13NO/c14-12-9-5-4-8-11(12)13(15)10-6-2-1-3-7-10/h1-9,13,15H,14H2/t13-/m1/s1

SMILES: c1ccc(cc1)[C@H](c1ccccc1N)O

Synonyms:

• (2-Aminophenyl)(Phenyl)Methanol
• A-O-Aminophenylbenzyl Alcohol
• O-Aminobenzhydrol
• O-Aminodiphenylcarbinol
• (R)-(2-aminophenyl)(phenyl)methanol

Benzenemethanol, 2-amino-α-phenyl-

CAS: 13209-38-6

Formula: C₁₃H₁₃NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 199.2484

Ref: IN-DA001072

2-Aminobenzhydrol

CAS: 13209-38-6

2-Aminobenzhydrol

Formula: C₁₃H₁₃NO

Purity: 97%

Color and Shape: off-white solid

Molecular weight: 199.25g/mol

Ref: 54-OR5164

2-Aminobenzhydrol

CAS: 13209-38-6

2-Aminobenzhydrol is a synthetic compound that has been shown to be an efficient and selective hydrogen donor for the copper-catalyzed reaction of arylgalactoses with anilines. It is a potent inhibitor of galactose oxidase, which catalyzes the conversion of glucose to galactose. 2-Aminobenzhydrol inhibits galactose oxidase by forming an intramolecular hydrogen bond with the main group amine nitrogen atom in the enzyme. This interaction results in a reversible, competitive inhibition with respect to substrate binding. 2-Aminobenzhydrol has shown potent inhibitory activity against other enzymes such as ceruloplasmine oxidase and urate oxidase.

Formula: C₁₃H₁₃NO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 199.25 g/mol

Ref: 3D-FA70205

2-Aminobenzhydrol

CAS: 13209-38-6

Formula: C₁₃H₁₃NO

Purity: 95%

Color and Shape: Solid

Molecular weight: 199.253

Ref: 10-F018171