1H-Imidazol-2-amine, 4,5-dihydro-4-phenyl-

Base Information

Chemical Name:1H-Imidazol-2-amine, 4,5-dihydro-4-phenyl-
CAS No.:89145-85-7
Molecular Formula:C9H11N3
Molecular Weight:161.206
Hs Code.:
ChEMBL ID:CHEMBL433716
DSSTox Substance ID:DTXSID40461535

Synonyms:1H-Imidazol-2-amine, 4,5-dihydro-4-phenyl-;89145-85-7;CHEMBL433716;SCHEMBL6438699;SCHEMBL13655204;DTXSID40461535;AKOS017531608

Suppliers and Price of 1H-Imidazol-2-amine, 4,5-dihydro-4-phenyl-

Supply Marketing:

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

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Chemical Property of 1H-Imidazol-2-amine, 4,5-dihydro-4-phenyl-

Chemical Property:

XLogP3:0.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:161.095297364
Heavy Atom Count:12
Complexity:182

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(NC(=N1)N)C2=CC=CC=C2

Technology Process of 1H-Imidazol-2-amine, 4,5-dihydro-4-phenyl-

There total 4 articles about 1H-Imidazol-2-amine, 4,5-dihydro-4-phenyl- 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:

: 2-(2,2,2-trichloroethoxysulfonylimino)-4-phenylimidazolidine

: 89145-85-7
4-phenyl-4,5-dihydro-1⁽³⁾H-imidazol-2-ylamine

Guidance literature:: With acetic acid; zinc; Rh₂(esp)2; In methanol; at 40 ℃; for 16h;
DOI:10.1021/ol052920y

Reference yield:

: 882739-51-7
[1-Amino-1-phenethylamino-meth-(Z)-ylidene]-sulfamic acid 2,2,2-trichloro-ethyl ester

: 89145-85-7
4-phenyl-4,5-dihydro-1⁽³⁾H-imidazol-2-ylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 57 percent / PhI(OAc)2; MgO / Rh2(α,α,α',α'-tetramethyl-1,3-benzenedipropionate)2 / toluene / 12 h / 40 °C

2: Zn; acetic acid / Rh2(α,α,α',α'-tetramethyl-1,3-benzenedipropionate)2 / methanol / 16 h / 40 °C

With [bis(acetoxy)iodo]benzene; magnesium oxide; acetic acid; zinc; Rh₂(esp)2; In methanol; toluene;
DOI:10.1021/ol052920y