N-(5-Chloro-2-methoxy-4-nitrophenyl)benzamide

Base Information

• Chemical Name: N-(5-Chloro-2-methoxy-4-nitrophenyl)benzamide
• CAS No.: 59385-63-6
• Molecular Formula: C14H11ClN2O4
• Molecular Weight: 306.705
• European Community (EC) Number: 261-730-5
• UNII: 42CVX8YF72
• DSSTox Substance ID: DTXSID40208109
• Nikkaji Number: J298.139D
• Wikidata: Q83082203
• Mol file: 59385-63-6.mol

Synonyms:N-(5-Chloro-2-methoxy-4-nitrophenyl)benzamide;59385-63-6;42CVX8YF72;EINECS 261-730-5;C14H11ClN2O4;benzamide, n-(5-chloro-2-methoxy-4-nitrophenyl)-;UNII-42CVX8YF72;Benzamide,N-(5-chloro-2-methoxy-4-nitrophenyl)-;Oprea1_058907;DTXSID40208109;C14-H11-Cl-N2-O4;STK396680;AKOS000435982;1-BENZAMIDO-5-CHLORO-2-METHOXY-4-NITROBENZENE

Chemical Property of N-(5-Chloro-2-methoxy-4-nitrophenyl)benzamide

Chemical Property:

• Vapor Pressure: 2.06E-06mmHg at 25°C
• Refractive Index: 1.651
• Boiling Point: 393.9 °C at 760 mmHg
• Flash Point: 192 °C
• PSA: 87.64000
• Density: 1.419 g/cm³
• LogP: 4.41630
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 306.0407345
• Heavy Atom Count: 21
• Complexity: 382

Purity/Quality:

99% ^*data from raw suppliers

N-(5-CHLORO-2-METHOXY-4-NITROPHENYL)BENZAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC(=C(C=C1NC(=O)C2=CC=CC=C2)Cl)[N+](=O)[O-]

Technology Process of N-(5-Chloro-2-methoxy-4-nitrophenyl)benzamide

There total 1 articles about N-(5-Chloro-2-methoxy-4-nitrophenyl)benzamide 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:

5-chloro-2-methoxy-4-nitroaniline (6259-08-1) + benzoyl chloride (98-88-4) → benzoic acid-(5-chloro-2-methoxy-4-nitro-anilide) (59385-63-6)

Guidance literature:

With diethyl ether; sodium carbonate;

Reference yield:

benzoic acid-(5-chloro-2-methoxy-4-nitro-anilide) (59385-63-6) → 2-chloro-4-benzoylamino-5-methoxy-aniline (6368-90-7)

Guidance literature:

With hydrogenchloride; zinc;

Reference yield:

benzoic acid-(5-chloro-2-methoxy-4-nitro-anilide) (59385-63-6) → N,N'-(2-chloro-5-methoxy-p-phenylene)-bis-benzamide (110877-27-5)

Guidance literature:

Multi-step reaction with 2 steps

1: aq.-ethanolic Na₂S₂O₄

With sodium dithionite;

DOI:10.1021/ja01571a050

upstream raw materials:

5-chloro-2-methoxy-4-nitroaniline

benzoyl chloride

Downstream raw materials:

2-chloro-4-benzoylamino-5-methoxy-aniline

N,N'-(2-chloro-5-methoxy-p-phenylene)-bis-benzamide

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