4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene

Base Information

Chemical Name:4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene
CAS No.:433226-28-9
Molecular Formula:C₁₅H₁₁N₃O₆
Molecular Weight:329.269
Hs Code.:
DSSTox Substance ID:DTXSID601271484

Synonyms:4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene;SCHEMBL5360724;DIBCJCIFVWDLIV-UHFFFAOYSA-N;DTXSID601271484;433226-28-9;N-[4-(3,4-dinitrobenzoyl)phenyl]acetamide

Suppliers and Price of 4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene

Supply Marketing:

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

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Chemical Property of 4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:329.06478508
Heavy Atom Count:24
Complexity:518

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=CC=C(C=C1)C(=O)C2=CC(=C(C=C2)[N+](=O)[O-])[N+](=O)[O-]

Technology Process of 4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene

There total 2 articles about 4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene 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:

: 24376-18-9
3,4-dinitrobenzoyl chloride

: 103-84-4
Acetanilid

: 433226-28-9
4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene

Guidance literature:: With aluminium trichloride; In dichloromethane; at 40 ℃; for 24h;
DOI:10.1021/jm0611051

Reference yield:

: 528-45-0
3,4-dinitrobenzoic acid

: 433226-28-9
4-(4-(Acetamido)phenylcarbonyl)-1,2-dinitrobenzene

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride

2: 87 mg / AlCl₃ / CH₂Cl₂ / 24 h / 40 °C

With aluminium trichloride; oxalyl dichloride; In dichloromethane;
DOI:10.1021/jm0611051