1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, ethyl ester

Base Information

Chemical Name:1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, ethyl ester
CAS No.:91332-09-1
Molecular Formula:C₁₁H₁₃N₃O₂
Molecular Weight:219.243
Hs Code.:
Mol file:91332-09-1.mol

Synonyms:ethyl 2-amino-1-methyl-1H-benzo[d]imidazole-5-carboxylate

Suppliers and Price of 1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, ethyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

AccelPharmtech
2-amino-1-methyl-1H-Benzimidazole-5-carboxylicacidethylester 97.00%
25G
$ 13300.00

AccelPharmtech
2-amino-1-methyl-1H-Benzimidazole-5-carboxylicacidethylester 97.00%
5G
$ 5360.00

AccelPharmtech
2-amino-1-methyl-1H-Benzimidazole-5-carboxylicacidethylester 97.00%
1G
$ 3120.00

A1 Biochem Labs
Ethyl2-amino-1-methyl-1H-benzo[d]imidazole-5-carboxylate 95%
2.5 g
$ 1400.00

Total 3 raw suppliers

Chemical Property of 1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, ethyl ester

Chemical Property:

Purity/Quality:: 2-amino-1-methyl-1H-Benzimidazole-5-carboxylicacidethylester 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, ethyl ester

There total 4 articles about 1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, ethyl ester 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:

: 506-68-3
bromocyane

: 66315-23-9
ethyl 3-amino-4-(methylamino)benzoate

: 91332-09-1
ethyl 2-amino-1-methyl-1H-benzo[d]imidazole-5-carboxylate

Guidance literature:: In tetrahydrofuran; water; at 50 ℃; for 16h;

Reference yield:

: 16588-16-2
ethyl 4-chloro-3-nitrobenzoate

: 91332-09-1
ethyl 2-amino-1-methyl-1H-benzo[d]imidazole-5-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: N,N-dimethyl-formamide / 16 h / 60 °C

2: hydrogen; palladium 10% on activated carbon / methanol; ethanol / 5 h / 20 °C / 3102.97 Torr / Inert atmosphere

3: tetrahydrofuran; water / 16 h / 50 °C

With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 71254-71-2
ethyl 4-(methylamino)-3-nitrobenzoate

: 91332-09-1
ethyl 2-amino-1-methyl-1H-benzo[d]imidazole-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen; palladium 10% on activated carbon / methanol; ethanol / 5 h / 20 °C / 3102.97 Torr / Inert atmosphere

2: tetrahydrofuran; water / 16 h / 50 °C

With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; ethanol; water;