N-(4-hydroxyphenyl)-4-nitrobenzamide

Base Information

• Chemical Name: N-(4-hydroxyphenyl)-4-nitrobenzamide
• CAS No.: 13160-56-0
• Molecular Formula: C13H10 N2 O4
• Molecular Weight: 258.233
• DSSTox Substance ID: DTXSID70408670
• NSC Number: 212083
• Wikidata: Q82214222

Synonyms:N-(4-hydroxyphenyl)-4-nitrobenzamide;13160-56-0;NSC 212083;Benzamide, N-(4-hydroxyphenyl)-4-nitro-;NSC212083;Oprea1_385565;Oprea1_806243;CBDivE_012355;SCHEMBL9137224;DTXSID70408670;AKOS001483330;NSC-212083;EU-0033512;SR-01000389441;SR-01000389441-1

Chemical Property of N-(4-hydroxyphenyl)-4-nitrobenzamide

Chemical Property:

• Vapor Pressure: 7.83E-07mmHg at 25°C
• Boiling Point: 395.8°Cat760mmHg
• Flash Point: 193.2°C
• Density: 1.446g/cm³
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 258.06405680
• Heavy Atom Count: 19
• Complexity: 326

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1C(=O)NC2=CC=C(C=C2)O)[N+](=O)[O-]

Technology Process of N-(4-hydroxyphenyl)-4-nitrobenzamide

There total 6 articles about N-(4-hydroxyphenyl)-4-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: 83.0%

N-hydroxy-N-phenyl-4-nitrobenzamide (2029-61-0) → N-(4-hydroxyphenyl)-4-nitrobenzamide (13160-56-0)

Guidance literature:

With Phenylselenyl bromide; In 1,4-dioxane; at 23 ℃; for 4h;

DOI:10.1002/anie.202100801

Reference yield: 74.0%

p-aminophenol hydrochloride (51-78-5) + 4-nitro-benzoyl chloride (122-04-3) → N-(4-hydroxyphenyl)-4-nitrobenzamide (13160-56-0)

Guidance literature:

With sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃; for 5h; Cooling with ice;

DOI:10.1016/j.ejmech.2013.07.056

Reference yield:

4-amino-phenol (123-30-8) + 4-nitro-benzoyl chloride (122-04-3) → N-(4-hydroxyphenyl)-4-nitrobenzamide (13160-56-0)

Guidance literature:

With sodium hydrogencarbonate; benzene;

upstream raw materials:

4-amino-phenol

4-nitro-benzoyl chloride

p-aminophenol hydrochloride

N-hydroxy-N-phenyl-4-nitrobenzamide

Downstream raw materials:

1-(4-nitro-benzoylamino)-4-(3,4,5-trimethoxy-benzoyloxy)-benzene

2-morpholin-4-ylmethyl-4-(4-nitro-benzoylamino)-phenol

N-(4-Hydroxy-3,5-bis-pyrrolidin-1-ylmethyl-phenyl)-4-nitro-benzamide

4-nitro-N-(4-oxocyclohexa-2,5-dien-1-ylidene)benzamide

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