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3-NITRODIBENZOTHIOPHENE

Base Information
  • Chemical Name:3-NITRODIBENZOTHIOPHENE
  • CAS No.:94764-55-3
  • Molecular Formula:C12H7NO2S
  • Molecular Weight:229.259
  • Hs Code.:2934999090
  • Mol file:94764-55-3.mol
3-NITRODIBENZOTHIOPHENE

Synonyms:3-Nitrodibenzothiophene

Suppliers and Price of 3-NITRODIBENZOTHIOPHENE
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
  • American Custom Chemicals Corporation
  • 3-NITRODIBENZOTHIOPHENE 95.00%
  • 5MG
  • $ 499.22
Total 8 raw suppliers
Chemical Property of 3-NITRODIBENZOTHIOPHENE
Chemical Property:
  • Vapor Pressure:5.88E-07mmHg at 25°C 
  • Boiling Point:422.5°C at 760 mmHg 
  • Flash Point:209.3°C 
  • PSA:74.06000 
  • Density:1.441g/cm3 
  • LogP:4.48590 
Purity/Quality:

99% *data from raw suppliers

3-NITRODIBENZOTHIOPHENE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 3-NITRODIBENZOTHIOPHENE

There total 12 articles about 3-NITRODIBENZOTHIOPHENE 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 hydrogen bromide; In water; acetic acid;
DOI:10.1021/jm900809r
Guidance literature:
With palladium dichloride; In dimethyl sulfoxide; at 140 ℃; for 12h; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.orglett.8b02347
Guidance literature:
With triethylammonium N-benzyldithiocarbamate; copper(II) sulfate; In acetonitrile; at 40 ℃; for 5h; Sealed tube; Inert atmosphere;
DOI:10.1002/adsc.201600405
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