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7-broMo-5-Methylbenzo[b]thiophene

Base Information Edit
  • Chemical Name:7-broMo-5-Methylbenzo[b]thiophene
  • CAS No.:19076-19-8
  • Molecular Formula:C9H7BrS
  • Molecular Weight:227.12088
  • Hs Code.:
  • Mol file:19076-19-8.mol
7-broMo-5-Methylbenzo[b]thiophene

Synonyms:7-broMo-5-Methylbenzo[b]thiophene

Suppliers and Price of 7-broMo-5-Methylbenzo[b]thiophene
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
  • Matrix Scientific
  • 7-Bromo-5-methylbenzo[b]thiophene 95%
  • 5g
  • $ 1876.00
  • Matrix Scientific
  • 7-Bromo-5-methylbenzo[b]thiophene 95%
  • 1g
  • $ 626.00
Total 1 raw suppliers
Chemical Property of 7-broMo-5-Methylbenzo[b]thiophene Edit
Chemical Property:
  • PSA:28.24000 
  • LogP:3.97220 
Purity/Quality:

95% *data from raw suppliers

7-Bromo-5-methylbenzo[b]thiophene 95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 7-broMo-5-Methylbenzo[b]thiophene

There total 2 articles about 7-broMo-5-Methylbenzo[b]thiophene 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 quinoline; copper(l) iodide; at 200 ℃; for 0.5h;
Guidance literature:
Multi-step reaction with 2 steps
1: sodium hydroxide; water / methanol; tetrahydrofuran / 12 h / 20 °C
2: copper(l) iodide; quinoline / 0.5 h / 200 °C
With quinoline; copper(l) iodide; water; sodium hydroxide; In tetrahydrofuran; methanol;
Guidance literature:
Multi-step reaction with 3 steps
1: 2-Methyl-2-nitropropane; N-hydroxyphthalimide; palladium diacetate / acetonitrile / 48 h / 80 °C / Inert atmosphere
2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium carbonate / N,N-dimethyl-formamide; water / 0.5 h / 90 °C / Inert atmosphere
3: sodium hydroxide; water / methanol; tetrahydrofuran / 12 h / 20 °C
With N-hydroxyphthalimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; 2-Methyl-2-nitropropane; water; palladium diacetate; potassium carbonate; sodium hydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetonitrile; 2: |Suzuki Coupling;
Refernces Edit
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