3-IMIDAZOL-1-YL-PHENYLAMINE

Base Information

• Chemical Name: 3-IMIDAZOL-1-YL-PHENYLAMINE
• CAS No.: 112677-67-5
• Molecular Formula: C9H9N3
• Molecular Weight: 159.191
• Hs Code.: 2933290090
• Mol file: 112677-67-5.mol

Synonyms:3-(1H-imidazol-1-yl)benzenamine;3-(imidazol-1-yl)aniline;3-imidazolylphenylamine;1-(3-amino)phenylimidazole;3-(1H-imidazol-1-yl)aniline;3-(imidazol-1-yl)phenylamine;Benzenamine,3-(1H-imidazol-1-yl);

Chemical Property of 3-IMIDAZOL-1-YL-PHENYLAMINE

Chemical Property:

• Melting Point: 112-114 °C
• Boiling Point: 373.1±25.0 °C(Predicted)
• PKA: 5.53±0.10(Predicted)
• PSA: 43.84000
• Density: 1.20±0.1 g/cm3(Predicted)
• LogP: 2.03570
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature

Purity/Quality:

99%, ^*data from raw suppliers

3-(1H-Imidazol-1-yl)aniline ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: 3-(1H-Imidazol-1-yl)aniline is a useful reagent for many copper-catalyzed reactions.

Technology Process of 3-IMIDAZOL-1-YL-PHENYLAMINE

There total 8 articles about 3-IMIDAZOL-1-YL-PHENYLAMINE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

1-(3-nitrophenyl)-1H-imidazole (23309-09-3) → 3-(1H-imidazol-1-yl)aniline (112677-67-5)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In acetic acid; for 3h; under 2585.81 Torr;

Reference yield: 99.0%

1H-imidazole (288-32-4) + m-Bromoaniline (591-19-5) → 3-(1H-imidazol-1-yl)aniline (112677-67-5)

Guidance literature:

With copper(l) iodide; potassium carbonate; L-proline; PS[DMVBIM][Pro]; In dimethyl sulfoxide; at 120 ℃; for 60h;

DOI:10.1021/ja073633n

Reference yield: 82.0%

1H-imidazole (288-32-4) + 3-Iodoaniline (626-01-7) → 3-(1H-imidazol-1-yl)aniline (112677-67-5)

Guidance literature:

With potassium phosphate; copper(l) iodide; 1,10-Phenanthroline; In 1,4-dioxane; at 110 ℃; for 24h; Inert atmosphere;

upstream raw materials:

1-(3-nitrophenyl)-1H-imidazole

1H-imidazole

m-Bromoaniline

3-fluoro-1-nitrobenzene

Downstream raw materials:

N-(3-(imidazol-1-yl)phenyl)-2-phenylthiazole-4-carboxamide

N-(5-bromo-3-nitropyridin-2-yl)-N-[3-(imidazol-1-yl)phenyl]amine

(3-imidazol-1ylphenyl)-(5-phenylisoquinolin-1-yl)amine

(5-bromoisoquinolin-1-yl)-[3-(imidazol-1-yl)phenyl]amine

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