CAS 7621-86-5

2-(4-Aminophenyl)-5-aminobenzimidazole

Description:

2-(4-Aminophenyl)-5-aminobenzimidazole, with the CAS number 7621-86-5, is an organic compound that belongs to the class of benzimidazoles, which are characterized by a fused benzene and imidazole ring structure. This compound features two amino groups, which contribute to its potential as a building block in pharmaceuticals and dyes. It typically appears as a crystalline solid and is soluble in polar solvents. The presence of amino groups enhances its reactivity, allowing for various chemical modifications. This compound may exhibit biological activity, making it of interest in medicinal chemistry, particularly in the development of anti-cancer or anti-inflammatory agents. Its molecular structure allows for hydrogen bonding, which can influence its interactions with biological targets. Safety data should be consulted for handling and exposure, as with any chemical substance, to ensure proper laboratory practices. Overall, 2-(4-Aminophenyl)-5-aminobenzimidazole is a versatile compound with potential applications in various fields of chemistry and biology.

Formula: C₁₃H₁₂N₄

InChI: InChI=1S/C13H12N4/c14-9-3-1-8(2-4-9)13-16-11-6-5-10(15)7-12(11)17-13/h1-7H,14-15H2,(H,16,17)

InChI key: InChIKey=XAFOTXWPFVZQAZ-UHFFFAOYSA-N

SMILES: NC1=CC=C(C=2NC=3C(N2)=CC(N)=CC3)C=C1

Synonyms:

• 1H-Benzimidazol-5-amine, 2-(4-aminophenyl)-
• 1H-Benzimidazol-6-amine, 2-(4-aminophenyl)-
• 2-(4-Amino-phenyl)-1H-benzoimidazol-5-ylamine
• 2-(4-Aminophenyl)-1H-1,3-benzodiazol-5-amine
• 2-(4-Aminophenyl)-1H-1,3-benzodiazol-6-amine
• 2-(4-Aminophenyl)-1H-benzimidazol-5-amine
• 2-(4-Aminophenyl)-1H-benzimidazole-5-amine
• 2-(4-Aminophenyl)-1H-benzo[d]imidazol-5-amine
• 2-(4-Aminophenyl)-3H-benzimidazol-5-amine
• 2-(4-Aminophenyl)-5-aminobenzimidazole
• 2-(4-aminophenyl)-1H-benzimidazol-6-amine
• 5(6)-Amino-2-(4′-aminophenyl)benzimidazole
• 5(6)-Amino-2-(p-aminophenyl)benzimidazole
• 5,4′-Diamino-2-phenylbenzimidazole
• 5-Amino-2-(4-aminobenzene)benzimidazole
• 5-Amino-2-(4-aminophenyl)-1H-benzimidazole
• 5-Amino-2-(4-aminophenyl)-benzimidazole
• 5-Amino-2-(4-aminophenyl)benzylimidazole
• 5-Amino-2-(p-aminophenyl)benzimidazole
• 6,4′-Diamino-2-phenylbenzimidazole
• Apbia
• Benzimidazole, 5(or 6)-amino-2-(p-aminophenyl)-
• Benzimidazole, 5-amino-2-(p-aminophenyl)-

5-Amino-2-(4-aminophenyl)benzimidazole

CAS: 7621-86-5

Formula: C₁₃H₁₂N₄

Purity: >98.0%(HPLC)

Color and Shape: White to Light orange to Yellow powder to crystal

Molecular weight: 224.27

Ref: 3B-A2759

2-(4-Aminophenyl)-1H-benzo[d]imidazol-5-amine

CAS: 7621-86-5

Formula: C₁₃H₁₂N₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 224.2612

Ref: IN-DA008O9H

5-Amino-2-(p-aminophenyl)benzimidazole

CAS: 7621-86-5

5-Amino-2-(p-aminophenyl)benzimidazole

Purity: 98%

Color and Shape: Solid

Molecular weight: 224.26g/mol

Ref: 54-OR323128

2-(4-Aminophenyl)-1H-benzo[d]imidazol-5-amine

CAS: 7621-86-5

Purity: 95.0%

Molecular weight: 224.26699829101562

Ref: 10-F211210

5-Amino-2-(4-aminophenyl)benzimidazole

CAS: 7621-86-5

5-Amino-2-(4-aminophenyl)benzimidazole is a chemical compound that is used in the synthesis of other compounds. It can be prepared by the reaction of 4-aminophenol with 2,5-dichlorobenzene imidazole followed by hydrogenation and purification. 5-Amino-2-(4-aminophenyl)benzimidazole has a high resistance to both UV and thermal degradation. It has been shown to have low solubility in water, but high solubility in organic solvents such as chloroform, ethyl acetate, and cyclohexane. This compound shows an orthorhombic crystal structure and reacts with proton (H+) or chloride ion. 5-Amino-2-(4-aminophenyl)benzimidazole is also used as a reagent for gel permeation chromatography in order to

Formula: C₁₃H₁₂N₄

Purity: Min. 95%

Molecular weight: 224.27 g/mol

Ref: 3D-HAA62186