1H-Imidazole-5-carboxamide, 1-methyl-4-(methylamino)-

Base Information

Chemical Name:1H-Imidazole-5-carboxamide, 1-methyl-4-(methylamino)-
CAS No.:64995-64-8
Molecular Formula:C6H10N4O
Molecular Weight:154.172
Hs Code.:
DSSTox Substance ID:DTXSID40542853
Wikidata:Q82419644

Synonyms:64995-64-8;1H-Imidazole-5-carboxamide, 1-methyl-4-(methylamino)-;3-methyl-5-(methylamino)imidazole-4-carboxamide;SCHEMBL18256648;DTXSID40542853;1-Methyl-4-(methylamino)-1H-imidazole-5-carboxamide

Suppliers and Price of 1H-Imidazole-5-carboxamide, 1-methyl-4-(methylamino)-

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

Total 1 raw suppliers

Chemical Property of 1H-Imidazole-5-carboxamide, 1-methyl-4-(methylamino)-

Chemical Property:

XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:154.08546096
Heavy Atom Count:11
Complexity:161

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC1=C(N(C=N1)C)C(=O)N

Technology Process of 1H-Imidazole-5-carboxamide, 1-methyl-4-(methylamino)-

There total 1 articles about 1H-Imidazole-5-carboxamide, 1-methyl-4-(methylamino)- 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: 1.0%

: 3,7-dimethyladenine hydriodide

: 64995-64-8
1-methyl-4-(N-methylamino)-1H-imidazole-5-carboxamide

: 19143-59-0
3,7-Dimethylhypoxanthin

Guidance literature:: With sodium hydroxide; at 80 ℃; for 0.5h; Yields of byproduct given;

Reference yield:

: 64995-64-8
1-methyl-4-(N-methylamino)-1H-imidazole-5-carboxamide

: 83-67-0
theobromine /

Guidance literature:: Multi-step reaction with 2 steps

1: aq. AcOH-AcONa buffer, 10 percent aq. NaOH / ethyl acetate / 2 h / Ambient temperature; pH 5.2-5.3

2: 1 N aq. NaOH / 0.17 h / Heating

With sodium hydroxide; AcOH-AcONa buffer; In ethyl acetate;
DOI:10.1248/cpb.39.2855

Reference yield:

: 64995-64-8
1-methyl-4-(N-methylamino)-1H-imidazole-5-carboxamide

: 55247-90-0
1-benzyl-3,7-dimethylxanthine

Guidance literature:: Multi-step reaction with 3 steps

1: aq. AcOH-AcONa buffer, 10 percent aq. NaOH / ethyl acetate / 2 h / Ambient temperature; pH 5.2-5.3

2: 1 N aq. NaOH / 0.17 h / Heating

3: 1.) K₂CO₃ / 1.) DMF, 80 deg C, 1 h, 2.) a) room temperature, 6 h, b) 95 deg C, 7 h

With sodium hydroxide; AcOH-AcONa buffer; potassium carbonate; In ethyl acetate;
DOI:10.1248/cpb.39.2855