p-Nitrobenzylidene-p-chlorophenylacetonitrile

Base Information

Chemical Name:p-Nitrobenzylidene-p-chlorophenylacetonitrile
CAS No.:104089-73-8
Molecular Formula:C15H9 Cl N2 O2
Molecular Weight:0
Hs Code.:2926909090
Mol file:104089-73-8.mol

Synonyms:p-Nitrobenzylidene-p-chlorophenylacetonitrile;104089-73-8;(Z)-2-(4-chlorophenyl)-3-(4-nitrophenyl)prop-2-enenitrile;SCHEMBL10389792;AKOS003398990;(2Z)-2-(4-chlorophenyl)-3-(4-nitrophenyl)acrylonitrile

Suppliers and Price of p-Nitrobenzylidene-p-chlorophenylacetonitrile

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 p-Nitrobenzylidene-p-chlorophenylacetonitrile

Chemical Property:

Vapor Pressure:3.09E-07mmHg at 25°C
Boiling Point:419.2°Cat760mmHg
Flash Point:207.3°C
PSA：69.61000
Density:1.357g/cm³
LogP:4.83558
XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:284.0352552
Heavy Atom Count:20
Complexity:419

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C=C(C#N)C2=CC=C(C=C2)Cl)[N+](=O)[O-]
Isomeric SMILES:C1=CC(=CC=C1/C=C(\C#N)/C2=CC=C(C=C2)Cl)[N+](=O)[O-]

Technology Process of p-Nitrobenzylidene-p-chlorophenylacetonitrile

There total 3 articles about p-Nitrobenzylidene-p-chlorophenylacetonitrile 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: 85.0%

: 555-16-8
4-nitrobenzaldehdye

: 140-53-4
p-chlorobenzyl cyanide

: 104089-73-8
2-(4-chloro-phenyl)-3-(4-nitro-phenyl)-acrylonitrile

Guidance literature:: With 18-crown-6 ether; graphitic carbon nitride; In toluene; at 25 ℃; for 0.5h;
DOI:10.1039/c7ra03051g

Reference yield:

: 104-83-6
1-Chloro-4-(chloromethyl)benzene

: 104089-73-8
2-(4-chloro-phenyl)-3-(4-nitro-phenyl)-acrylonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: alcohol; water

2: alcohol; alkali

With ethanol; water;

Reference yield:

: 108-88-3,15644-74-3,16713-13-6
toluene

: 104089-73-8
2-(4-chloro-phenyl)-3-(4-nitro-phenyl)-acrylonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: durch Chlorieren

2: alcohol; water

3: alcohol; alkali

With ethanol; water;