N-(p-Methoxybenzylidene)-p-nitroaniline

Base Information

• Chemical Name: N-(p-Methoxybenzylidene)-p-nitroaniline
• CAS No.: 15450-66-5
• Molecular Formula: C14H12 N2 O3
• Molecular Weight: 256.261
• NSC Number: 95598
• Nikkaji Number: J1.064.586G
• Mol file: 15450-66-5.mol

Synonyms:N-(p-Methoxybenzylidene)-p-nitroaniline;Aniline, N-(p-methoxybenzylidene)-p-nitro-;4-(4-Methoxybenzylideneamino)nitrobenzene;Benzenamine, N-((4-methoxyphenyl)methylene)-4-nitro-;Benzenamine, N-[(4-methoxyphenyl)methylene]-4-nitro-;p-methoxybenzylidene-(4-nitrophenyl)-amine;N-[(4-Methoxyphenyl)methylidene]-4-nitroaniline;NSC95598;N-(4-Methoxybenzylidene)-4-nitroaniline;NCIOpen2_005994;SCHEMBL3431012;YZJSVLVRDFIMHX-XNTDXEJSSA-N;NSC-95598;AKOS024334850;4-nitro-4'-methoxy-N-benzylideneaniline;15450-66-5;(4-Methoxy-benzyliden)-(4-nitro-phenyl)-amin;(4-Methoxy-benzylidene)-(4-nitro-phenyl)-amin

Chemical Property of N-(p-Methoxybenzylidene)-p-nitroaniline

Chemical Property:

• Vapor Pressure: 2.87E-07mmHg at 25°C
• Boiling Point: 432.1°C at 760 mmHg
• Flash Point: 215.1°C
• Density: 1.18g/cm³
• XLogP3: 3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 256.08479225
• Heavy Atom Count: 19
• Complexity: 311

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C=NC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of N-(p-Methoxybenzylidene)-p-nitroaniline

There total 3 articles about N-(p-Methoxybenzylidene)-p-nitroaniline 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: 100.0%

4-methoxy-benzaldehyde (123-11-5) + 4-nitro-aniline (100-01-6,104810-17-5) → N-(4-methoxybenzylidene)-4-nitroaniline (15450-66-5)

Guidance literature:

With pyrrolidine; In dichloromethane; at 20 ℃; for 16h; Molecular sieve;

DOI:10.1021/ja4111418

Reference yield:

4-nitro-aniline (100-01-6,104810-17-5) + 4-Methoxybenzyl alcohol (105-13-5) → N-(4-methoxybenzylidene)-4-nitroaniline (15450-66-5)

Guidance literature:

With potassium hydroxide; In toluene; at 110 ℃; for 30h;

DOI:10.1021/acs.inorgchem.6b02592

Reference yield:

→ N-(4-methoxybenzylidene)-4-nitroaniline (15450-66-5)

Guidance literature:

p-H3CO-C6H4-CHO, p-H2N-C6H4-NO2;

upstream raw materials:

4-methoxy-benzaldehyde

4-nitro-aniline

4-Methoxybenzyl alcohol

Downstream raw materials:

diphenyl 1-(4-nitrophenylamino)-1-(4-methoxyphenyl)methanephosphonate

1-(p-nitrophenyl)-3-phenoxy-4-(p-methoxyphenyl)-azetidin-2-one

2-(4-methoxyphenyl)-1-(4-nitrophenyl)-2,3-dihydropyridin-4(1H)-one

4-(4-methoxyphenyl)-3-(4-nitrophenyl)-1,3-oxazetidin-2-one

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