1-(Ethenyloxy)-3-nitrobenzene

Base Information

Chemical Name:1-(Ethenyloxy)-3-nitrobenzene
CAS No.:1441-07-2
Molecular Formula:C8H7NO3
Molecular Weight:165.148
Hs Code.:
DSSTox Substance ID:DTXSID50560402
Nikkaji Number:J799.342K
Wikidata:Q82443539

Synonyms:1441-07-2;1-(Ethenyloxy)-3-nitrobenzene;vinyl m-nitrophenyl ether;1-Nitro-3-vinyloxy-benzene;SCHEMBL3392074;DTXSID50560402;AKOS015711535

Suppliers and Price of 1-(Ethenyloxy)-3-nitrobenzene

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of 1-(Ethenyloxy)-3-nitrobenzene

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:165.042593085
Heavy Atom Count:12
Complexity:176

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=COC1=CC=CC(=C1)[N+](=O)[O-]

Technology Process of 1-(Ethenyloxy)-3-nitrobenzene

There total 4 articles about 1-(Ethenyloxy)-3-nitrobenzene 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: 78.0%

: C₁₃H₁₈N₂O₄

: 1441-07-2
p-Nitrophenylvinylether

Guidance literature:: With N,O-bis-(trimethylsilyl)-acetamide; In toluene; for 0.416667h; Reflux;
DOI:10.1016/j.tet.2021.132108

Reference yield:

: 891855-93-9
1-(2-(3-nitrophenoxy)ethyl)piperidine

: 1441-07-2
p-Nitrophenylvinylether

Guidance literature:: Multi-step reaction with 2 steps

1: peracetic acid; acetic acid / dichloromethane / 0.08 h

2: N,O-bis-(trimethylsilyl)-acetamide / toluene / 0.42 h / Reflux

With peracetic acid; N,O-bis-(trimethylsilyl)-acetamide; acetic acid; In dichloromethane; toluene; 2: |Cope Elimination;
DOI:10.1016/j.tet.2021.132108