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2,6-Naphthalenedithiol

Base Information Edit
  • Chemical Name:2,6-Naphthalenedithiol
  • CAS No.:96892-95-4
  • Molecular Formula:C10H8S2
  • Molecular Weight:192.306
  • Hs Code.:2930909090
  • Mol file:96892-95-4.mol
2,6-Naphthalenedithiol

Synonyms:2,6-Dithionaphthalene;Naphthalene-2,6-dithiol;

Suppliers and Price of 2,6-Naphthalenedithiol
Supply Marketing:Edit
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
  • TRC
  • Naphthalene-2,6-dithiol
  • 1mg
  • $ 45.00
  • Matrix Scientific
  • 2,6-Naphthalenedithiol 98%
  • 100mg
  • $ 121.00
  • Crysdot
  • Naphthalene-2,6-dithiol 97%
  • 100mg
  • $ 208.00
  • American Custom Chemicals Corporation
  • 2,6-NAPHTHALENEDITHIOL 95.00%
  • 100MG
  • $ 710.33
Total 55 raw suppliers
Chemical Property of 2,6-Naphthalenedithiol Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.747 
  • Boiling Point:353.7 ºC at 760 mmHg 
  • Flash Point:178.6 ºC 
  • PSA:77.60000 
  • Density:1.292 g/cm3 
  • LogP:3.41720 
Purity/Quality:

99% *data from raw suppliers

Naphthalene-2,6-dithiol *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Naphthalene-2,6-dithiol can be used in the preparation of polyaromatic ether. It can also be used to manufacture silicone rubber and in a cosmetic process for attenuating wrinkles.
Technology Process of 2,6-Naphthalenedithiol

There total 5 articles about 2,6-Naphthalenedithiol 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 hydrogenchloride; tin(ll) chloride; In acetic acid; at 90 ℃; for 2h;

Reference yield: 60.0%

Guidance literature:
Guidance literature:
Multi-step reaction with 2 steps
1: 71 percent / PCl5 / 4 h / 130 °C
2: 69 percent / SnCl2, HCl(g) / acetic acid / 2 h / 90 °C
With hydrogenchloride; phosphorus pentachloride; tin(ll) chloride; In acetic acid;
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