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Thiophene, 3,3'-thiobis-

Base Information
  • Chemical Name:Thiophene, 3,3'-thiobis-
  • CAS No.:3807-38-3
  • Molecular Formula:C8H6S3
  • Molecular Weight:198.334
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70191479
  • Nikkaji Number:J1.853.680C
  • Wikidata:Q83064000
  • Mol file:3807-38-3.mol
Thiophene, 3,3'-thiobis-

Synonyms:Thiophene, 3,3'-thiobis-;3807-38-3;Di(thiophen-3-yl)sulfane;3-thiophen-3-ylsulfanylthiophene;Di-(3-thienyl)sulfide;Thiophene,3,3'-thiobis-;di(3-thienyl)sulfide;3,3'-Thiobisthiophene;SCHEMBL6665571;3-(3-Thienylsulfanyl)thiophene;DTXSID70191479;3-(3-Thienylsulfanyl)thiophene #

Suppliers and Price of Thiophene, 3,3'-thiobis-
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 3 raw suppliers
Chemical Property of Thiophene, 3,3'-thiobis-
Chemical Property:
  • Boiling Point:315°Cat760mmHg 
  • Flash Point:144.3°C 
  • Density:1.37g/cm3 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:197.96316371
  • Heavy Atom Count:11
  • Complexity:113
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CSC=C1SC2=CSC=C2
Technology Process of Thiophene, 3,3'-thiobis-

There total 1 articles about Thiophene, 3,3'-thiobis- 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 dimethylselenide; hydrogen sulfide; In gas; at 500 ℃; Product distribution; Mechanism; effect of dimethyl selenide on reaction; various temperatures;
Guidance literature:
sulfure de dithienyle-3,3'; With n-butyllithium; In diethyl ether; hexane; at -3 - 40 ℃; for 2.5h; Inert atmosphere;
dimethoxy(mesityl)borane; In diethyl ether; hexane;
Guidance literature:
Multi-step reaction with 4 steps
1.1: n-butyllithium / diethyl ether / 1 h / 0 - 40 °C / Inert atmosphere
1.2: 0 °C / Inert atmosphere
2.1: acetic acid; N-Bromosuccinimide / chloroform / 3 h / 0 - 20 °C
3.1: n-butyllithium; N-ethyl-N,N-diisopropylamine; lithium diisopropyl amide / tetrahydrofuran / 2 h / -78 - 20 °C / Inert atmosphere
4.1: n-butyllithium / diethyl ether / 0.5 h / -78 °C / Inert atmosphere
4.2: -78 - 20 °C / Inert atmosphere
With N-Bromosuccinimide; n-butyllithium; acetic acid; N-ethyl-N,N-diisopropylamine; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; chloroform;
DOI:10.1002/anie.201410970
upstream raw materials:

2-thienyl chloride

Downstream raw materials:

2,6-dibromodithieno[3,2-b:2',3'-d]thiophene

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