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3,4-Dimethoxybenzenethiolate

Base Information Edit
  • Chemical Name:3,4-Dimethoxybenzenethiolate
  • CAS No.:19689-66-8
  • Molecular Formula:C8H10O2S
  • Molecular Weight:170.232
  • Hs Code.:2930909090
  • DSSTox Substance ID:DTXSID00941449
  • Nikkaji Number:J2.302.867K
  • Wikidata:Q82918292
  • Mol file:19689-66-8.mol
3,4-Dimethoxybenzenethiolate

Synonyms:3,4-dimethoxybenzenethiolate;3,4-Dimethoxybenzene-1-thiolate;DTXSID00941449

Suppliers and Price of 3,4-Dimethoxybenzenethiolate
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
  • 3,5-Dimethoxythiophenol
  • 1g
  • $ 165.00
  • Rieke Metals
  • 3,5-DIMETHOXYBENZENETHIOL
  • 5g
  • $ 1943.00
  • Rieke Metals
  • 3,5-DIMETHOXYBENZENETHIOL
  • 1g
  • $ 809.00
  • American Custom Chemicals Corporation
  • 3,5-DIMETHOXYTHIOPHENOL 95.00%
  • 5MG
  • $ 498.66
Total 10 raw suppliers
Chemical Property of 3,4-Dimethoxybenzenethiolate Edit
Chemical Property:
  • Vapor Pressure:0.0173mmHg at 25°C 
  • Refractive Index:1.5090 (estimate) 
  • Boiling Point:262.9 °C at 760 mmHg 
  • PKA:6.14±0.11(Predicted) 
  • Flash Point:112.8 °C 
  • PSA:57.26000 
  • Density:1.134 g/cm3 
  • LogP:1.99250 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:169.03232570
  • Heavy Atom Count:11
  • Complexity:119
Purity/Quality:

98%min *data from raw suppliers

3,5-Dimethoxythiophenol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=C(C=C(C=C1)[S-])OC
  • Uses 3,5-Dimethoxythiophenol is used in the synthesis of arylthioindoles as potent inhibitors of tubulin polymerization.
Technology Process of 3,4-Dimethoxybenzenethiolate

There total 8 articles about 3,4-Dimethoxybenzenethiolate 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 potassium hydroxide; In methanol; for 2h; Reflux;
Guidance literature:
C11H14O3S2; With potassium hydroxide; In ethanol; at 80 ℃; for 16h;
With hydrogenchloride; In water; pH=1;
With lithium aluminium tetrahydride; In diethyl ether; at 0 - 25 ℃; for 2h; Inert atmosphere;
DOI:10.1021/acs.macromol.6b00629
Guidance literature:
Multi-step reaction with 3 steps
1.1: NaH / dimethylformamide
1.2: 47 percent / dimethylformamide / Heating
2.1: 100 percent / 6 h / 285 °C
3.1: 99 percent / KOH / methanol / Heating
With potassium hydroxide; sodium hydride; In methanol; N,N-dimethyl-formamide; 2.1: Newman-Kwart rearrangement;
DOI:10.1021/jm0493109
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