CAS 52708-36-8

4-(1H-Benzimidazol-1-yl)benzenamine

Description:

4-(1H-Benzimidazol-1-yl)benzenamine, with the CAS number 52708-36-8, is an organic compound characterized by the presence of both a benzimidazole and an aniline moiety. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents. Its structure features a benzimidazole ring, which contributes to its potential biological activity, including antimicrobial and anticancer properties. The amine group in the aniline part of the molecule can participate in hydrogen bonding, influencing its reactivity and interactions with other chemical species. The compound may also exhibit fluorescence properties, making it of interest in various applications, including materials science and medicinal chemistry. Additionally, its synthesis often involves straightforward organic reactions, making it accessible for research purposes. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity.

Formula: C₁₃H₁₁N₃

InChI: InChI=1/C13H11N3/c14-10-5-7-11(8-6-10)16-9-15-12-3-1-2-4-13(12)16/h1-9H,14H2

InChI key: InChIKey=DWYMPMWWYZEKLQ-UHFFFAOYSA-N

SMILES: NC1=CC=C(N2C=3C(N=C2)=CC=CC3)C=C1

Synonyms:

• 1-(4-Aminophenyl)-1H-benzimidazole
• 1-(4-Aminophenyl)benzimidazole
• 1-(p-Aminophenyl)benzimidazole
• 4-(1H-Benzimidazol-1-yl)benzenamine
• T56 Bn Dnj Br Dz
• benzenamine, 4-(1H-benzimidazol-1-yl)-
• 4-(1H-Benzo[d]imidazol-1-yl)aniline
• 4-(1H-benzimidazol-1-yl)aniline(SALTDATA: FREE)
• 4-(benzimidazol-1-yl)aniline

4-(1H-Benzo[d]imidazol-1-yl)aniline

CAS: 52708-36-8

4-(1H-Benzo[d]imidazol-1-yl)aniline is an aromatic compound that is used as a catalyst in organic chemistry. It is also used to synthesize polysubstituted imidazoles and ammonium acetate, which are used in the production of polyaromatic hydrocarbons. This compound has been shown to catalyze the formation of benzil from benzaldehyde and ammonium chloride. This reaction can be accelerated by adding ammonium hydroxide solution. 4-(1H-Benzo[d]imidazol-1-yl)aniline has also been used to synthesize imidazoles by reacting with aldehydes such as formaldehyde, acetaldehyde, or propionaldehyde.

Formula: C₁₃H₁₁N₃

Purity: Min. 95%

Molecular weight: 209.25 g/mol

Ref: 3D-CCA70836