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2-BROMO-4-METHYLTHIOBENZAMIDE

Base Information
  • Chemical Name:2-BROMO-4-METHYLTHIOBENZAMIDE
  • CAS No.:1208076-70-3
  • Molecular Formula:C8H8BrNS
  • Molecular Weight:230.128
  • Hs Code.:
  • Mol file:1208076-70-3.mol
2-BROMO-4-METHYLTHIOBENZAMIDE

Synonyms:C8H8BrNS

Suppliers and Price of 2-BROMO-4-METHYLTHIOBENZAMIDE
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
  • SynQuest Laboratories
  • 2-Bromo-4-methylthiobenzamide 98%
  • 1 g
  • $ 69.00
  • SynQuest Laboratories
  • 2-Bromo-4-methylthiobenzamide 98%
  • 5 g
  • $ 276.00
  • Matrix Scientific
  • 2-Bromo-4-methylthiobenzamide 98%
  • 5g
  • $ 235.00
  • Matrix Scientific
  • 2-Bromo-4-methylthiobenzamide 98%
  • 1g
  • $ 67.00
  • Crysdot
  • 2-Bromo-4-Methylbenzothioamide 95+%
  • 10g
  • $ 329.00
  • AK Scientific
  • 2-Bromo-4-methylthiobenzamide
  • 2.5g
  • $ 326.00
Total 7 raw suppliers
Chemical Property of 2-BROMO-4-METHYLTHIOBENZAMIDE
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

2-Bromo-4-methylthiobenzamide 98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-BROMO-4-METHYLTHIOBENZAMIDE

There total 2 articles about 2-BROMO-4-METHYLTHIOBENZAMIDE 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:

Reference yield: 95.5%

Guidance literature:
With sodium hydrogen sulfide; carbon dioxide; In N,N-dimethyl-formamide; at 25 ℃; under 7500.75 Torr; Autoclave;
Guidance literature:
With Lawessons reagent; In tetrahydrofuran; at 23 ℃; for 1h;
DOI:10.1016/j.bmc.2011.09.031
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