1-ethoxy-2,4-dinitronaphthalene

Base Information

• Chemical Name: 1-ethoxy-2,4-dinitronaphthalene
• CAS No.: 15352-94-0
• Molecular Formula: C12H10 N2 O5
• Molecular Weight: 262.222
• Mol file: 15352-94-0.mol

Synonyms:1-Ethoxy-2,4-dinitronaphthalene;2,4-Dinitro-1-naphthyl ethyl ether; NSC 298144

Chemical Property of 1-ethoxy-2,4-dinitronaphthalene

Chemical Property:

• Vapor Pressure: 8.75E-08mmHg at 25°C
• Boiling Point: 447.6°C at 760 mmHg
• Flash Point: 210°C
• Density: 1.396g/cm³

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 1-ethoxy-2,4-dinitronaphthalene

There total 2 articles about 1-ethoxy-2,4-dinitronaphthalene 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:

C16H18N3O5(1-) → pyrrolidine (123-75-1) + ethyl ether of 2,4-dinitro-1-naphthol (15352-94-0)

Guidance literature:

In dimethyl sulfoxide; at 25 ℃; Equilibrium constant; kinetic of reactions of cyclic secondary amines (pyrrolidine, piperidine) with 2,4-dinitro-1-naphthyl ethyl ether in DMSO; stage I kinetics and equilibrium (with pyrrolidine);

DOI:10.1021/ja00406a032

Reference yield:

C17H20N3O5(1-) (53359-90-3) → piperidine (110-89-4) + ethyl ether of 2,4-dinitro-1-naphthol (15352-94-0)

Guidance literature:

In dimethyl sulfoxide; at 25 ℃; Rate constant; Equilibrium constant; Mechanism; kinetic of reactions of cyclic secondary amines (pyrrolidine, piperidine) with 2,4-dinitro-1-naphthyl ethyl ether in DMSO; stage I kinetics and equilibrium (with piperidine);

DOI:10.1021/ja00406a032

Reference yield:

pyrrolidine (123-75-1) + ethyl ether of 2,4-dinitro-1-naphthol (15352-94-0) → ethanol (64-17-5) + 1-(pyrrolidinyl)-2,4-dinitronaphthalene (78521-30-9)

Guidance literature:

In dimethyl sulfoxide; at 25 ℃; Rate constant; Mechanism; kinetic of reactions of cyclic secondary amines (pyrrolidine, piperidine) with 2,4-dinitro-1-naphthyl ethyl ether in DMSO; stage I and II kinetics (with pyrrolidine); reaction in the presence of pyrrolidinium and N,N-dimethylpyrrolidinium chlorides;

DOI:10.1021/ja00406a032

upstream raw materials:

C₁₇H₂₀N₃O₅^(1-)

Downstream raw materials:

ethanol

1-(pyrrolidinyl)-2,4-dinitronaphthalene

2,4-dinitro-1-(1-piperidyl)naphthalene