4-Nitrophenyl 2-ethoxyprop-2-enoate

Base Information

Chemical Name:4-Nitrophenyl 2-ethoxyprop-2-enoate
CAS No.:108818-44-6
Molecular Formula:C₁₁H₁₁NO₅
Molecular Weight:237.212
Hs Code.:
DSSTox Substance ID:DTXSID90550089
Wikidata:Q82429304
Mol file:108818-44-6.mol

Synonyms:108818-44-6;4-Nitrophenyl 2-ethoxyprop-2-enoate;DTXSID90550089

Suppliers and Price of 4-Nitrophenyl 2-ethoxyprop-2-enoate

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 4-Nitrophenyl 2-ethoxyprop-2-enoate

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:237.06372245
Heavy Atom Count:17
Complexity:302

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=C)C(=O)OC1=CC=C(C=C1)[N+](=O)[O-]

Technology Process of 4-Nitrophenyl 2-ethoxyprop-2-enoate

There total 2 articles about 4-Nitrophenyl 2-ethoxyprop-2-enoate 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: 82.0%

: 658-78-6
1-nitro-4-trifluoroacetoxy-benzene

: 32821-76-4
α-Ethoxyacrylic acid

: 108818-44-6
p-nitrophenyl 2-ethoxypropenoate

Guidance literature:: With pyridine; for 24h; Ambient temperature;
DOI:10.1021/jo00391a068

Reference yield:

: 25741-02-0
2,2-diethoxypropionic acid

: 108818-44-6
p-nitrophenyl 2-ethoxypropenoate

Guidance literature:: Multi-step reaction with 2 steps

1: 40 percent / 100 °C / 1.5 Torr

2: 82 percent / pyridine / 24 h / Ambient temperature

With pyridine;
DOI:10.1021/jo00391a068