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cis-4-Mononitrostilbene

Base Information
  • Chemical Name:cis-4-Mononitrostilbene
  • CAS No.:6624-53-9
  • Molecular Formula:C14H11NO2
  • Molecular Weight:225.247
  • Hs Code.:
  • Nikkaji Number:J995.370A
cis-4-Mononitrostilbene

Synonyms:cis-4-Mononitrostilbene;6624-53-9;cis-4-Nitrostilbene;(Z)-4-Nitrostilbene;1-nitro-4-[(Z)-2-phenylethenyl]benzene;(Z)-1-Nitro-4-styrylbenzene;4-Nitro-trans-stilbene;Stilbene, 4-nitro-, (Z)-;4-nitro-cis-stilbene;p-Nitro-trans-stilbene;Benzene, 1-nitro-4-(2-phenylethenyl)-, (Z)-;BDBM175266;BAA69420;NSC 53390;Trans-1-Nitro-4-styrylbenzene (5);AS-78166;N1085;T72796

Suppliers and Price of cis-4-Mononitrostilbene
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 7 raw suppliers
Chemical Property of cis-4-Mononitrostilbene
Chemical Property:
  • Vapor Pressure:0.000145mmHg at 25°C 
  • Boiling Point:342.8°C at 760 mmHg 
  • Flash Point:153.5°C 
  • Density:1.22g/cm3 
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:225.078978594
  • Heavy Atom Count:17
  • Complexity:268
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C=CC2=CC=C(C=C2)[N+](=O)[O-]
  • Isomeric SMILES:C1=CC=C(C=C1)/C=C\C2=CC=C(C=C2)[N+](=O)[O-]
Technology Process of cis-4-Mononitrostilbene

There total 164 articles about cis-4-Mononitrostilbene 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:
Guidance literature:
With potassium carbonate; In ethanol; water; at 90 ℃; for 10h; Green chemistry;
DOI:10.1016/j.apcata.2014.02.002
Guidance literature:
With triethylamine; In water; acetonitrile; at 60 ℃; for 2h;
DOI:10.1080/00958972.2019.1687890
Guidance literature:
With dibutyl telluride; triethylamine; In acetonitrile; for 2h; Ambient temperature;
DOI:10.1080/00304949609355916
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