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Thieno[3,2-b:4,5-b']bis[1]benzothiophene

Base Information
  • Chemical Name:Thieno[3,2-b:4,5-b']bis[1]benzothiophene
  • CAS No.:241-13-4
  • Molecular Formula:C16H8S3
  • Molecular Weight:296.438
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40571582
  • Nikkaji Number:J2.248.910K,J2.062.666F
  • Wikidata:Q82459710
  • Mol file:241-13-4.mol
Thieno[3,2-b:4,5-b']bis[1]benzothiophene

Synonyms:Thieno[3,2-b:4,5-b']bis[1]benzothiophene;241-13-4;3,11,19-trithiapentacyclo[10.7.0.02,10.04,9.013,18]nonadeca-1(12),2(10),4,6,8,13,15,17-octaene;SCHEMBL349784;YSCK0015;DTXSID40571582;10.14272/PDGITMHDEWXSAM-UHFFFAOYSA-N;doi:10.14272/PDGITMHDEWXSAM-UHFFFAOYSA-N;[1]Benzothieno[2',3':4,5]thieno[3,2-b][1]benzothiophene

Suppliers and Price of Thieno[3,2-b:4,5-b']bis[1]benzothiophene
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
  • Crysdot
  • Thieno[3,2-b:4,5-b']bis[1]benzothiophene 95+%
  • 1g
  • $ 1353.00
  • Alichem
  • Thieno[3,2-b:4,5-b']bis[1]benzothiophene
  • 1g
  • $ 1083.06
Total 17 raw suppliers
Chemical Property of Thieno[3,2-b:4,5-b']bis[1]benzothiophene
Chemical Property:
  • PSA:84.72000 
  • LogP:6.48390 
  • XLogP3:6.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:295.97881378
  • Heavy Atom Count:19
  • Complexity:337
Purity/Quality:

99%, *data from raw suppliers

Thieno[3,2-b:4,5-b']bis[1]benzothiophene 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C3=C(S2)C4=C(S3)C5=CC=CC=C5S4
Technology Process of Thieno[3,2-b:4,5-b']bis[1]benzothiophene

There total 27 articles about Thieno[3,2-b:4,5-b']bis[1]benzothiophene 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:
3,4-bis(methylthio)-2,5-diphenylthiophene; With dihydrogen peroxide; acetic acid; for 12h; Heating;
With trifluorormethanesulfonic acid; In dichloromethane; at 20 ℃; for 24h;
With pyridine; In dichloromethane; water; for 0.5h; Reflux;
DOI:10.1002/adsc.201401159
Guidance literature:
With trifluorormethanesulfonic acid; In dichloromethane; at 0 - 20 ℃; for 12h; Inert atmosphere;
DOI:10.1021/ol501006t
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