Acetamide, 2-(4-chlorophenoxy)-N-((6-nitro-1H-benzimidazol-1-yl)methyl)-

Base Information

Chemical Name:Acetamide, 2-(4-chlorophenoxy)-N-((6-nitro-1H-benzimidazol-1-yl)methyl)-
CAS No.:103706-84-9
Molecular Formula:C₁₆H₁₃ClN₄O₄
Molecular Weight:360.757
Hs Code.:
DSSTox Substance ID:DTXSID50146023
Mol file:103706-84-9.mol

Synonyms:2-(4-Chlorophenoxy)-N-((6-nitro-1H-benzimidazol-1-yl)methyl)acetamide;Acetamide, 2-(4-chlorophenoxy)-N-((6-nitro-1H-benzimidazol-1-yl)methyl)-;103706-84-9;DTXSID50146023;LS-8631

Suppliers and Price of Acetamide, 2-(4-chlorophenoxy)-N-((6-nitro-1H-benzimidazol-1-yl)methyl)-

Supply Marketing:

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

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Chemical Property of Acetamide, 2-(4-chlorophenoxy)-N-((6-nitro-1H-benzimidazol-1-yl)methyl)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：105.46000
Density:1.48g/cm³
LogP:4.11410
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:360.0625326
Heavy Atom Count:25
Complexity:481

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1OCC(=O)NCN2C=NC3=C2C=C(C=C3)[N+](=O)[O-])Cl

Technology Process of Acetamide, 2-(4-chlorophenoxy)-N-((6-nitro-1H-benzimidazol-1-yl)methyl)-

There total 2 articles about Acetamide, 2-(4-chlorophenoxy)-N-((6-nitro-1H-benzimidazol-1-yl)methyl)- 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:

: 99-56-9
4-Nitrophenylene-1,2-diamine

: 103706-84-9
2-(4-Chloro-phenoxy)-N-(6-nitro-benzoimidazol-1-ylmethyl)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 4N HCl

2: conc. HCl / ethanol / 3 h / Heating

With hydrogenchloride; In ethanol;