Description
2-(3-Aminophenyl)-1H-benzo[d]imidazol-5-amine (CAS No. 13676-49-8) is a high-purity benzimidazole derivative with the molecular formula C13H12N4. This compound features a benzimidazole core substituted with an aminophenyl group at the 2-position and an additional amine group at the 5-position, making it a versatile intermediate for organic synthesis and pharmaceutical research. Its precise structure, validated by NMR and HPLC analysis, ensures optimal performance in specialized applications. Ideal for researchers and scientists, this product is supplied with comprehensive analytical data, including purity (>98%) and batch-specific certificates of analysis. Store in a cool, dry place under inert conditions to maintain stability.
Properties
- CAS Number: 13676-49-8
- Complexity: 270
- IUPAC Name: 2-(3-aminophenyl)-3H-benzimidazol-5-amine
- InChI: InChI=1S/C13H12N4/c14-9-3-1-2-8(6-9)13-16-11-5-4-10(15)7-12(11)17-13/h1-7H,14-15H2,(H,16,17)
- InChI Key: QCILMAMLEHOLRX-UHFFFAOYSA-N
- Exact Mass: 224.106196400
- Molecular Formula: C13H12N4
- Molecular Weight: 224.26
- SMILES: C1=CC(=CC(=C1)N)C2=NC3=C(N2)C=C(C=C3)N
- Topological: 80.7
- Monoisotopic Mass: 224.106196400
- Synonyms: 2-(3-aminophenyl)-1h-benzimidazol-6-amine, 2-(3-Aminophenyl)-1H-benzo[d]imidazol-5-amine, 2-(3-Aminophenyl)-1H-benzo(d)imidazol-5-amine, 988-207-0, 13676-49-8, 2-(3-Aminophenyl)-1H-benzo[d]imidazol-6-amine, 2-(3-aminophenyl)-3H-benzimidazol-5-amine, 2-(3-aminophenyl)-5-aminobenzimidazole, 1H-Benzimidazol-6-amine, 2-(3-aminophenyl)-, 1233518-22-3, MFCD13874743, Oprea1_149177, Oprea1_219714, SCHEMBL9767334, SCHEMBL9767339, DTXSID00275498, AKOS000635203, AKOS030524044, CCG-103253, DS-19236, DB-181224, CS-0161645, EU-0033588, D71030, SR-01000390480, SR-01000390480-1
Application
2-(3-Aminophenyl)-1H-benzo[d]imidazol-5-amine is a key intermediate in the synthesis of heterocyclic compounds, particularly in pharmaceutical and agrochemical research. Its reactive amine groups enable facile functionalization, making it valuable for designing novel drug candidates or ligands for metal-organic frameworks. Researchers also utilize this compound in dye chemistry and as a building block for polymers with tailored electronic properties. Its benzimidazole core contributes to potential biological activity, including antimicrobial or antitumor applications.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
Precautionary Statements
- P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2 (100%)
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