1-(3-Chloro-propenyl)-3-nitro-benzene

Base Information

Chemical Name:1-(3-Chloro-propenyl)-3-nitro-benzene
CAS No.:2016-83-3
Molecular Formula:C9H8ClNO2
Molecular Weight:197.621
Hs Code.:
European Community (EC) Number:654-603-4

Synonyms:m-nitrocinnamyl chloride;3-nitro-cinnamyl chloride;VYHWMGGPQOROGN-UHFFFAOYSA-N;AKOS017517959;1-(3-CHLORO-PROPENYL)-3-NITRO-BENZENE

Suppliers and Price of 1-(3-Chloro-propenyl)-3-nitro-benzene

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 1 raw suppliers

Chemical Property of 1-(3-Chloro-propenyl)-3-nitro-benzene

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:197.0243562
Heavy Atom Count:13
Complexity:200

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 1-(3-Chloro-propenyl)-3-nitro-benzene

There total 4 articles about 1-(3-Chloro-propenyl)-3-nitro-benzene 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: 68.0%

: 1504-64-9
(E)-3-(3-nitrophenyl)prop-2-en-1-ol

: 2016-83-3
(E)-(3-chloroprop-1-enyl)-3-nitrobenzene

Guidance literature:: With thionyl chloride; In diethyl ether; at 0 - 20 ℃;
DOI:10.1002/ardp.200700062

Reference yield:

: 1504-64-9
3-(3-nitrophenyl)prop-2-en-1-ol

: 2016-83-3
3-Chlor-1-(3-nitro-phenyl)-prop-1-en

Guidance literature:: With hydrogenchloride;
DOI:10.1021/jm00327a010

Reference yield:

: 1504-76-3
3-nitrocinnamaldehyde

: 2016-83-3
3-Chlor-1-(3-nitro-phenyl)-prop-1-en

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄

2: aq. HCl

With hydrogenchloride; sodium tetrahydroborate;
DOI:10.1021/jm00327a010