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

Base Information

Chemical Name:1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, Methyl ester
CAS No.:1258070-65-3
Molecular Formula:C₁₀H₁₁N₃O₂
Molecular Weight:205.216
Hs Code.:
Mol file:1258070-65-3.mol

Synonyms:methyl 2-amino-1-methyl-1H-1,3-benzodiazole-5-carboxylate

Suppliers and Price of 1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, Methyl 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-carboxylicacidmethylester 97.00%
5G
$ 3230.00

AccelPharmtech
2-amino-1-methyl-1H-Benzimidazole-5-carboxylicacidmethylester 97.00%
1G
$ 1890.00

Total 2 raw suppliers

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

Chemical Property:

Purity/Quality:

98% ^*data from raw suppliers

2-amino-1-methyl-1H-Benzimidazole-5-carboxylicacidmethylester 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-, Methyl ester

There total 3 articles about 1H-BenziMidazole-5-carboxylic acid, 2-aMino-1-Methyl-, Methyl 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: 96.0%

: 506-68-3
bromocyane

: 66315-16-0
methyl 3-amino-4-(methylamino)benzoate

: 1258070-65-3
methyl 2-amino-1-methyl-1H-1,3-benzodiazole-5-carboxylate

Guidance literature:: In tetrahydrofuran; water; at 20 - 50 ℃; for 4h;

Reference yield:

: 329-59-9
4-fluoro-3-nitro-benzoic acid methyl ester

: 1258070-65-3
methyl 2-amino-1-methyl-1H-1,3-benzodiazole-5-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide; tetrahydrofuran / 4 h / 20 °C

2: hydrogen; palladium on activated charcoal / methanol; dichloromethane

3: methanol / 20 °C

With palladium on activated charcoal; hydrogen; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 36242-50-9
4-methylamino-3-nitro-benzoic acid methyl ester

: 1258070-65-3
methyl 2-amino-1-methyl-1H-1,3-benzodiazole-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen; palladium on activated charcoal / methanol; dichloromethane

2: methanol / 20 °C

With palladium on activated charcoal; hydrogen; In methanol; dichloromethane;