4-(5-Chloro-1H-benzoimidazol-2-yl)-phenylamine
- CAS No.
- 39861-21-7
- Chemical Name:
- 4-(5-Chloro-1H-benzoimidazol-2-yl)-phenylamine
- Synonyms
- 4-(6-chloro-1h-benzimidazol-2-yl)aniline;4-(5-Chloro-1H-benzo[d]imidazol-2-yl)aniline;4-(5-Chloro-1H-benzoimidazol-2-yl)-phenylamine;Benzenamine, 4-(6-chloro-1H-benzimidazol-2-yl)-
- CBNumber:
- CB7258972
- Molecular Formula:
- C13H10ClN3
- Molecular Weight:
- 243.69
- MDL Number:
- MFCD00443934
- MOL File:
- Mol file
- MSDS File:
- SDS
SAFETY
Risk and Safety Statements
| Symbol(GHS) | ![]() GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H302-H315-H319-H335 |
| Precautionary statements | P261-P305+P351+P338 |
| Hazard Codes | Xi |
| HazardClass | IRRITANT |
4-(5-Chloro-1H-benzoimidazol-2-yl)-phenylamine price More Price(26)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Synthonix | C38943 | 4-(5-Chloro-1H-benzo[d]imidazol-2-yl)aniline 95+% | 39861-21-7 | 100mg | $90 | 2026-05-06 | Buy |
| Synthonix | C38943 | 4-(5-Chloro-1H-benzo[d]imidazol-2-yl)aniline 95+% | 39861-21-7 | 250mg | $97 | 2026-05-06 | Buy |
| Synthonix | C38943 | 4-(5-Chloro-1H-benzo[d]imidazol-2-yl)aniline 95+% | 39861-21-7 | 1g | $100 | 2026-05-06 | Buy |
| aablocks | AA00BZYX | 4-(5-Chloro-1H-Benzo[d]Imidazol-2-Yl)Aniline ≥95% | 39861-21-7 | 250mg | $32 | 2026-05-28 | Buy |
| aablocks | AA00BZYX | 4-(5-Chloro-1H-Benzo[d]Imidazol-2-Yl)Aniline ≥95% | 39861-21-7 | 1g | $90 | 2026-05-28 | Buy |
4-(5-Chloro-1H-benzoimidazol-2-yl)-phenylamine Chemical Properties,Uses,Production
Synthesis
150-13-0
95-83-0
39861-21-7
General procedure for the synthesis of 4-(5-chloro-1H-benzo[d]imidazol-2-yl)aniline from p-aminobenzoic acid and 4-chloro-1,2-benzenediamine: Eaton's reagent (10% v/v (w/v)) was added drop-wise to a mixture of 4-chloro-1,2-benzenediamine (1 equiv) and p-aminobenzoic acid (1 equiv). Subsequently, the reaction mixture was heated at 130 °C for 5-6 h. The reaction process was monitored by TLC and LCMS. After completion of the reaction, the mixture was cooled to room temperature and neutralized with 10% sodium hydroxide solution to pH 6-7. The precipitate formed was collected by filtration and washed repeatedly with water and subsequently dried. Finally, the resulting solid was purified by ethanol recrystallization to afford the target product 4-(5-chloro-1H-benzo[d]imidazol-2-yl)aniline in good yield.
References
[1] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 21, p. 5970 - 5987
4-(5-Chloro-1H-benzoimidazol-2-yl)-phenylamine Preparation Products And Raw materials
4-(5-Chloro-1H-benzoimidazol-2-yl)-phenylamine Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
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