2-(3-aminophenyl)-5-aminobenzimidazole

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Products Intro: Product Name:2-(3-aminophenyl)-5-aminobenzimidazole(2,3,5-ABA)
CAS:13676-49-8
Purity:99% Package:1kg;|20kg;
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Products Intro: Product Name:2-(3-aminophenyl)-5-aminobenzimidazole
CAS:13676-49-8
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CAS:13676-49-8
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Products Intro: Product Name:2-(3-aminophenyl)-5-aminobenzimidazole
CAS:13676-49-8
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Products Intro: Product Name:2-(3-aminophenyl)-5-aminobenzimidazole
CAS:13676-49-8
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2-(3-aminophenyl)-5-aminobenzimidazole manufacturers

2-(3-aminophenyl)-5-aminobenzimidazole Basic information
Product Name:2-(3-aminophenyl)-5-aminobenzimidazole
Synonyms:2-(3-aminophenyl)-5-aminobenzimidazole;2-(3-Aminophenyl)-1H-benzo[d]imidazol-6-amine;1H-Benzimidazol-5-amine, 2-(3-aminophenyl)-;2-(3-aminophenyl)-3H-benzimidazol-5-amine;2,3,5-ABA;1H-Benzimidazol-6-amine, 2-(3-aminophenyl)-;3-(3-aminophenyl)-5-aminobenzimi dazole (2,3,5-ABA);2-(3'-aminophenyI)- -5- -aminobenzimidazole
CAS:13676-49-8
MF:C13H12N4
MW:224.26
EINECS:206-141-6
Product Categories:
Mol File:13676-49-8.mol
2-(3-aminophenyl)-5-aminobenzimidazole Structure
2-(3-aminophenyl)-5-aminobenzimidazole Chemical Properties
Boiling point 562.7±56.0 °C(Predicted)
density 1.359±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka10.89±0.10(Predicted)
color Pale Beige to Pale Brown
Safety Information
MSDS Information
2-(3-aminophenyl)-5-aminobenzimidazole Usage And Synthesis
Synthesis
Benzamide, N-(2,4-dinitrophenyl)-3-nitro-

59403-35-9

2-(3-aminophenyl)-5-aminobenzimidazole

13676-49-8

The general procedure for the synthesis of 2-(3-aminophenyl)-5-aminobenzimidazole using the compound (CAS: 59403-35-9) as starting material was as follows: the prepared amide, 200 mL of acetic acid and 0.20 g of 5% Pd/C catalyst were added to a 500 mL autoclave. The reaction was carried out at 110 °C and 6 MPa hydrogen pressure for 4 hours. Upon completion of the reaction, the autoclave was cooled and filtered to recover the catalyst. About 150 mL of solvent was removed by distillation of the filtrate at atmospheric pressure under nitrogen protection. Subsequently, 100 mL of pure water was added to the remaining solution and the mixture was cooled to 20 °C. Upon filtration, 16.2 g of the target product 2-(3-aminophenyl)-5-aminobenzimidazole was obtained in 96.2% purity and 90.5% yield by HPLC.

References[1] Patent: CN107474016, 2017, A. Location in patent: Paragraph 0019-0020
[2] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 3, p. 711
2-(3-aminophenyl)-5-aminobenzimidazole Preparation Products And Raw materials
Raw materialsBenzamide, N-(2,4-dinitrophenyl)-3-nitro--->Hydrogen-->Palladium-->Activated carbon-->Acetic acid
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