N-(4-bromophenyl)-4,5-dihydro-1H-imidazol-2-amine

Base Information

Chemical Name:N-(4-bromophenyl)-4,5-dihydro-1H-imidazol-2-amine
CAS No.:63346-73-6
Molecular Formula:C₉H₁₀BrN₃
Molecular Weight:240.102
Hs Code.:
ChEMBL ID:CHEMBL3277529
DSSTox Substance ID:DTXSID80879438
Nikkaji Number:J1.606.962K
Wikidata:Q82861550

Synonyms:N-(4-bromophenyl)-4,5-dihydro-1H-imidazol-2-amine;63346-73-6;CHEMBL3277529;DTXSID80879438;2-(4-BR PHENYLIMINO)IMIDAZOLIDINE;EN300-738491

Suppliers and Price of N-(4-bromophenyl)-4,5-dihydro-1H-imidazol-2-amine

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-(4-bromophenyl)-4,5-dihydro-1H-imidazol-2-amine

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:239.00581
Heavy Atom Count:13
Complexity:197

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN=C(N1)NC2=CC=C(C=C2)Br

Technology Process of N-(4-bromophenyl)-4,5-dihydro-1H-imidazol-2-amine

There total 2 articles about N-(4-bromophenyl)-4,5-dihydro-1H-imidazol-2-amine 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: 93.0%

: 1286251-25-9
amino(4-bromophenylimino)methanesulfonic acid

: 107-15-3,85404-18-8
ethylenediamine

: 63346-73-6,773792-82-8
NC 12

Guidance literature:: In isopropyl alcohol; at 60 ℃; for 4h;
DOI:10.1002/cjoc.201190179

Reference yield:

: 26197-93-3
p-bromothiobanzamide

: 63346-73-6,773792-82-8
NC 12

Guidance literature:: Multi-step reaction with 2 steps

1: sodium molybdate; dihydrogen peroxide; sodium chloride / water / 0 - 30 °C

2: isopropyl alcohol / 4 h / 60 °C

With sodium molybdate; dihydrogen peroxide; sodium chloride; In water; isopropyl alcohol;
DOI:10.1002/cjoc.201190179