2-[2-(2-Nitrophenyl)ethenyl]aniline

Base Information

• Chemical Name: 2-[2-(2-Nitrophenyl)ethenyl]aniline
• CAS No.: 69395-24-0
• Molecular Formula: C14H12N2O2
• Molecular Weight: 0
• DSSTox Substance ID: DTXSID50702961
• Mol file: 69395-24-0.mol

Synonyms:Benzenamine, 2-[2-(2-nitrophenyl)ethenyl]-;DTXSID50702961;69395-24-0;2-[2-(2-Nitrophenyl)ethenyl]aniline

Chemical Property of 2-[2-(2-Nitrophenyl)ethenyl]aniline

Chemical Property:

• PSA: 71.84000
• LogP: 4.45180
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 240.089877630
• Heavy Atom Count: 18
• Complexity: 311

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)C=CC2=CC=CC=C2[N+](=O)[O-])N

Technology Process of 2-[2-(2-Nitrophenyl)ethenyl]aniline

There total 15 articles about 2-[2-(2-Nitrophenyl)ethenyl]aniline 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: 92.0%

(Z)-2-amino-2'-nitrostilbene (251089-08-4) → (E)-2-amino-2'-nitrostilbene (69395-24-0)

Guidance literature:

With 2,2'-azobis(isobutyronitrile); thiophenol; In benzene; for 2h; Heating;

DOI:10.1016/S0040-4020(01)00597-X

Reference yield: 86.0%

C26H37N2O2P → (E)-2-amino-2'-nitrostilbene (69395-24-0) + (Z)-2-amino-2'-nitrostilbene (251089-08-4)

Guidance literature:

With hydrogenchloride; water; In tetrahydrofuran; at 20 ℃; for 24h;

DOI:10.1016/S0040-4020(01)00597-X

Reference yield:

(2-nitrobenzyl)triphenylphosphonium bromide (23308-83-0) → (E)-2-amino-2'-nitrostilbene (69395-24-0)

Guidance literature:

Multi-step reaction with 3 steps

1: 85 percent / K₂CO₃; dibenzo-18-crown-6 / CH₂Cl₂ / 16 h / 20 °C

2: tetrahydrofuran / 1 h / 20 °C

3: 14 percent / HCl; H₂O / tetrahydrofuran / 24 h / 20 °C

With hydrogenchloride; dibenzo-18-crown-6; water; potassium carbonate; In tetrahydrofuran; dichloromethane; 2: Staudinger reaction;

DOI:10.1016/S0040-4020(01)00597-X

upstream raw materials:

1,2-bis(o-nitrophenyl)ethylene

N-<(2'-nitrostilben-2-yl)phenyl>-tert-butylcarbamate

2,2'-dinitrostilbene

(Z)-2-amino-2'-nitrostilbene

Downstream raw materials:

N-<(2'-nitrostilben-2-yl)phenyl>-p-methoxyphenylcarbamate

C₁₅H₁₀N₂O₃

neocryptolepine

1-methyl-3-(o-aminophenyl)-1H-quinoline-2-one