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5-Bromo-2-methylbenzenethiol

Base Information Edit
  • Chemical Name:5-Bromo-2-methylbenzenethiol
  • CAS No.:69321-55-7
  • Molecular Formula:C7H7BrS
  • Molecular Weight:203.103
  • Hs Code.:
  • European Community (EC) Number:865-668-5
  • Mol file:69321-55-7.mol
5-Bromo-2-methylbenzenethiol

Synonyms:5-Bromo-2-methylbenzenethiol;69321-55-7;5-Bromo-2-methylbenzene-1-thiol;SCHEMBL5424955;SFFDMQAUOUPZMM-UHFFFAOYSA-N;AT20875;CS-0257551;EN300-673792

Suppliers and Price of 5-Bromo-2-methylbenzenethiol
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
Total 1 raw suppliers
Chemical Property of 5-Bromo-2-methylbenzenethiol Edit
Chemical Property:
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:201.94518
  • Heavy Atom Count:9
  • Complexity:94.9
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1=C(C=C(C=C1)Br)S
Technology Process of 5-Bromo-2-methylbenzenethiol

There total 5 articles about 5-Bromo-2-methylbenzenethiol 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:
S-5-bromo-2-methylphenyl O-ethylcarbonodithioate; With potassium hydroxide; In ethanol; for 5h; Reflux;
With hydrogenchloride; In ethanol; water;
DOI:10.1039/c3ob40250a
Guidance literature:
5-bromo-2-methylaniline; With hydrogenchloride; sodium nitrite; In water; at -10 - -5 ℃; for 0.666667h;
With potassium ethyl xanthogenate; In water; at 65 ℃; for 0.833333h;
With potassium hydroxide; In ethanol; for 18h; Reflux;
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydrogenchloride; sodium nitrite / water / 2.5 h / 0 °C / Reflux
1.2: 1 h
2.1: potassium hydroxide / ethanol / 5 h / Reflux
With hydrogenchloride; potassium hydroxide; sodium nitrite; In ethanol; water;
DOI:10.1039/c3ob40250a
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