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2,3-Dimethyldibenzothiophene

Base Information
  • Chemical Name:2,3-Dimethyldibenzothiophene
  • CAS No.:31317-17-6
  • Molecular Formula:C14H12 S
  • Molecular Weight:212.315
  • Hs Code.:2934999090
  • DSSTox Substance ID:DTXSID40424044
  • Nikkaji Number:J570.937G
  • Wikidata:Q82236456
  • Mol file:31317-17-6.mol
2,3-Dimethyldibenzothiophene

Synonyms:2,3-dimethyldibenzothiophene;31317-17-6;2,3-dimethyl-dibenzothiophene;SCHEMBL12925865;DTXSID40424044;KEIKATUAMBEIQN-UHFFFAOYSA-N;2,3-Dimethyldibenzo[b,d]thiophene;FT-0709942;6-Chloro-N-(2,6-difluorophenyl)-4-(trifluoromethyl)nicotinamide

Suppliers and Price of 2,3-Dimethyldibenzothiophene
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
  • 2,3-DIMETHYLDIBENZOTHIOPHENE 98.00%
  • 5MG
  • $ 497.13
Total 3 raw suppliers
Chemical Property of 2,3-Dimethyldibenzothiophene
Chemical Property:
  • Boiling Point:369.4±11.0 °C(Predicted) 
  • PSA:28.24000 
  • Density:1.181±0.06 g/cm3(Predicted) 
  • LogP:4.67130 
  • XLogP3:5.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:212.06597156
  • Heavy Atom Count:15
  • Complexity:238
Purity/Quality:

99% *data from raw suppliers

2,3-DIMETHYLDIBENZOTHIOPHENE 98.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC2=C(C=C1C)SC3=CC=CC=C32
Technology Process of 2,3-Dimethyldibenzothiophene

There total 8 articles about 2,3-Dimethyldibenzothiophene 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:
Multi-step reaction with 4 steps
1: 1. conc. hydrochloric acid, NaNO2; / 1. 0 degC, 30min.; 2. 40 - 45 degC
2: 95 percent / LiAlH4 / diethyl ether / 3 h / Heating
3: 81 percent / NaOH / aq. ethanol / r.t., 30min., then reflux, 4h
4: 1. polyphosphoric acid; 2. Se powder / 1. 190-200 degC, 1.5h; 2. 300 degC, 8h
With hydrogenchloride; sodium hydroxide; selenium; lithium aluminium tetrahydride; PPA; sodium nitrite; In diethyl ether; ethanol;
Guidance literature:
Multi-step reaction with 2 steps
1: 81 percent / NaOH / aq. ethanol / r.t., 30min., then reflux, 4h
2: 1. polyphosphoric acid; 2. Se powder / 1. 190-200 degC, 1.5h; 2. 300 degC, 8h
With sodium hydroxide; selenium; PPA; In ethanol;
Guidance literature:
Multi-step reaction with 2 steps
1: 81 percent / NaOH / aq. ethanol / r.t., 30min., then reflux, 4h
2: 1. polyphosphoric acid; 2. Se powder / 1. 190-200 degC, 1.5h; 2. 300 degC, 8h
With sodium hydroxide; selenium; PPA; In ethanol;
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