Acetamide, N-(2-nitrophenyl)-N-2-propenyl-

Base Information

Chemical Name:Acetamide, N-(2-nitrophenyl)-N-2-propenyl-
CAS No.:107616-24-0
Molecular Formula:C11H12N2O3
Molecular Weight:220.228
Hs Code.:
DSSTox Substance ID:DTXSID60445392
Nikkaji Number:J2.033.789C
Wikidata:Q82263769
Mol file:107616-24-0.mol

Synonyms:107616-24-0;Acetamide, N-(2-nitrophenyl)-N-2-propenyl-;o-nitro-N-allylacetanilide;DTXSID60445392;ADAL1242929;N-Allyl-N-(2-nitrophenyl)acetamide;N-(2-NITROPHENYL)-N-(PROP-2-EN-1-YL)ACETAMIDE

Suppliers and Price of Acetamide, N-(2-nitrophenyl)-N-2-propenyl-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Acetamide, N-(2-nitrophenyl)-N-2-propenyl-

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:220.08479225
Heavy Atom Count:16
Complexity:285

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Acetamide, N-(2-nitrophenyl)-N-2-propenyl-

There total 2 articles about Acetamide, N-(2-nitrophenyl)-N-2-propenyl- 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: 88.0%

: 552-32-9
o-nitroacetanilide

: 106-95-6
allyl bromide

: 107616-24-0
N-(2-nitrophenyl)-N-(2-propenyl)acetamide

Guidance literature:: With potassium hydroxide; In acetone; for 0.05h; Heating;
DOI:10.1021/jo00386a007

Reference yield:

: 88-74-4
2-nitro-aniline

: 107616-24-0
N-(2-nitrophenyl)-N-(2-propenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 94.5 percent / conc. H₂SO₄ / benzene / 4 h / Heating

2: 68 percent / NaH / tetrahydrofuran / 1.) 0.5 h, 2.) 12 h

With sulfuric acid; sodium hydride; In tetrahydrofuran; benzene;
DOI:10.1039/a607060d