5-Amino-1-(benzyloxy)-1H-imidazole-4-carbonitrile

Base Information

Chemical Name:5-Amino-1-(benzyloxy)-1H-imidazole-4-carbonitrile
CAS No.:61193-35-9
Molecular Formula:C11H10N4O
Molecular Weight:214.227
Hs Code.:
DSSTox Substance ID:DTXSID40493619
Nikkaji Number:J1.163.708F
Wikidata:Q82340411

Synonyms:61193-35-9;5-Amino-1-(benzyloxy)-1H-imidazole-4-carbonitrile;5-amino-1-phenylmethoxyimidazole-4-carbonitrile;DTXSID40493619

Suppliers and Price of 5-Amino-1-(benzyloxy)-1H-imidazole-4-carbonitrile

Supply Marketing:

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

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Chemical Property of 5-Amino-1-(benzyloxy)-1H-imidazole-4-carbonitrile

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:214.08546096
Heavy Atom Count:16
Complexity:268

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CON2C=NC(=C2N)C#N

Technology Process of 5-Amino-1-(benzyloxy)-1H-imidazole-4-carbonitrile

There total 4 articles about 5-Amino-1-(benzyloxy)-1H-imidazole-4-carbonitrile 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: 82.0%

: 245126-93-6
(Z)-N-(2-Amino-1,2-dicyanovinyl)formamide O-benzyloxime

: 61193-35-9
5-amino-1-benzyloxyimidazole-4-carbonitrile

Guidance literature:: With potassium hydroxide; at 20 ℃; for 0.0833333h;
DOI:10.1039/a901332f

Reference yield:

: 622-33-3
N-benzyloxyamine

: 61193-35-9
5-amino-1-benzyloxyimidazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / tetrahydrofuran / 96 h / 20 °C

2: 82 percent / aq. KOH / 0.08 h / 20 °C

With potassium hydroxide; In tetrahydrofuran; 1: Condensation / 2: Cyclization;
DOI:10.1039/a901332f

Reference yield:

: 2687-43-6
O-benzylhydoxylamine hydrochloride

: 61193-35-9
5-amino-1-benzyloxyimidazole-4-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / aq. NaOH / diethyl ether / 3 h / Heating

2: 82 percent / aq. KOH / 0.08 h / 20 °C

With potassium hydroxide; sodium hydroxide; In diethyl ether; 1: Condensation / 2: Cyclization;
DOI:10.1039/a901332f