N-(4-methoxy-2-nitrophenyl)-3-nitrobenzamide

Base Information

Chemical Name:N-(4-methoxy-2-nitrophenyl)-3-nitrobenzamide
CAS No.:313497-60-8
Molecular Formula:C₁₄H₁₁N₃O₆
Molecular Weight:317.258
Hs Code.:
European Community (EC) Number:632-721-7

Synonyms:N-(4-methoxy-2-nitrophenyl)-3-nitrobenzamide;N-(4-Methoxy-2-nitro-phenyl)-3-nitro-benzamide;Oprea1_165192;STK055902;AKOS000604530;EU-0000313

Suppliers and Price of N-(4-methoxy-2-nitrophenyl)-3-nitrobenzamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-(4-methoxy-2-nitrophenyl)-3-nitrobenzamide

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:317.06478508
Heavy Atom Count:23
Complexity:460

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC(=C(C=C1)NC(=O)C2=CC(=CC=C2)[N+](=O)[O-])[N+](=O)[O-]

Technology Process of N-(4-methoxy-2-nitrophenyl)-3-nitrobenzamide

There total 3 articles about N-(4-methoxy-2-nitrophenyl)-3-nitrobenzamide 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:

: 101971-72-6
N-(4'-methoxyphenyl)-3-nitrobenzamide

: 313497-60-8
3-nitro-benzoic acid-(4-methoxy-2-nitro-anilide)

Guidance literature:: With nitric acid; acetic acid; at 80 ℃;

Reference yield:

: 104-94-9
4-methoxy-aniline

: 313497-60-8
3-nitro-benzoic acid-(4-methoxy-2-nitro-anilide)

Guidance literature:: Multi-step reaction with 2 steps

1: alcohol; sodium acetate

2: glacial acetic acid; nitric acid / 80 °C

With ethanol; nitric acid; sodium acetate; acetic acid;

Reference yield:

: 121-90-4
m-nitrobenzoic acid chloride

: 313497-60-8
3-nitro-benzoic acid-(4-methoxy-2-nitro-anilide)

Guidance literature:: Multi-step reaction with 2 steps

1: alcohol; sodium acetate

2: glacial acetic acid; nitric acid / 80 °C

With ethanol; nitric acid; sodium acetate; acetic acid;