CAS 3743-28-0

m-Hydroxybenzanilide

Description:

m-Hydroxybenzanilide, also known as 3-hydroxybenzanilide, is an organic compound characterized by the presence of both an aniline and a hydroxyl group on a benzene ring. Its molecular structure features a benzene ring substituted with a hydroxyl group at the meta position relative to the anilide group. This compound typically appears as a white to off-white solid and is sparingly soluble in water but more soluble in organic solvents such as ethanol and acetone. m-Hydroxybenzanilide exhibits properties that make it useful in various applications, including as an intermediate in organic synthesis and in the production of dyes and pharmaceuticals. The presence of the hydroxyl group contributes to its potential reactivity, allowing for further chemical modifications. Additionally, it may exhibit biological activity, which can be of interest in medicinal chemistry. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₃H₁₁NO₂

InChI: InChI=1/C13H11NO2/c15-12-8-4-5-10(9-12)13(16)14-11-6-2-1-3-7-11/h1-9,15H,(H,14,16)

SMILES: c1ccc(cc1)N=C(c1cccc(c1)O)O

Synonyms:

• Benzamide, N-(3-hydroxyphenyl)-
• N-(3-Hydroxyphenyl)benzamide
• 3-hydroxy-N-phenylbenzamide

BENZAMIDE, N-(3-HYDROXYPHENYL)-

CAS: 3743-28-0

Formula: C₁₃H₁₁NO₂

Purity: 99%

Color and Shape: Solid

Molecular weight: 213.2319

Ref: IN-DA0079RB

N-(3-Hydroxyphenyl)Benzamide

CAS: 3743-28-0

N-(3-Hydroxyphenyl)Benzamide

Purity: 99%

Molecular weight: 213.23g/mol

Ref: 54-OR1024915

3-Hydroxy-N-phenylbenzamide

CAS: 3743-28-0

3-Hydroxy-N-phenylbenzamide (3HB) is a chemical compound that has been isolated from the plant Caryophyllaceae. This compound is an electrophile, which can react with nucleophiles in biological systems. 3HB produces anthranilic acid when it reacts with amino acids, and this compound may be responsible for the antimicrobial activity of 3HB. 3HB was shown to have fungitoxic effects against some fungi including Fusarium oxysporum, Rhizoctonia solani, and Stemphylium sp., but not against other fungi such as Alternaria alternata and Penicillium cyclopium. The phytoalexin caryophyllin, which is produced by infected plants, also inhibits fungal growth.

Formula: C₁₃H₁₁NO₂

Purity: Min. 95%

Molecular weight: 213.23 g/mol

Ref: 3D-DAA74328