I+/--Acetyl-N-(3-ethylphenyl)-4-nitrobenzenepropanamide

Base Information

Chemical Name:I+/--Acetyl-N-(3-ethylphenyl)-4-nitrobenzenepropanamide
CAS No.:152456-68-3
Molecular Formula:C₁₉H₂₀N₂O₄
Molecular Weight:340.379
Hs Code.:
DSSTox Substance ID:DTXSID601221227

Synonyms:SCHEMBL9309184;DTXSID601221227;152456-68-3;I+/--Acetyl-N-(3-ethylphenyl)-4-nitrobenzenepropanamide

Suppliers and Price of I+/--Acetyl-N-(3-ethylphenyl)-4-nitrobenzenepropanamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of I+/--Acetyl-N-(3-ethylphenyl)-4-nitrobenzenepropanamide

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:340.14230712
Heavy Atom Count:25
Complexity:480

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1=CC(=CC=C1)NC(=O)C(CC2=CC=C(C=C2)[N+](=O)[O-])C(=O)C

Technology Process of I+/--Acetyl-N-(3-ethylphenyl)-4-nitrobenzenepropanamide

There total 3 articles about I+/--Acetyl-N-(3-ethylphenyl)-4-nitrobenzenepropanamide 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: 75.0%

: 152456-66-1
N-(3-ethylphenyl)-3-oxobutyramide

: 152456-68-3
N-(3-ethylphenyl)-2-(4-nitrobenzyl)-3-oxobutyramide

Guidance literature:: With potassium tert-butylate; In N,N-dimethyl-formamide; for 5h; Ambient temperature;

Reference yield:

: 587-02-0
m-ethylaniline

: 152456-68-3
N-(3-ethylphenyl)-2-(4-nitrobenzyl)-3-oxobutyramide

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / xylene / 0.5 h / 120 °C

2: 75 percent / t-BuOK / dimethylformamide / 5 h / Ambient temperature

With potassium tert-butylate; In N,N-dimethyl-formamide; xylene;