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4-Bromo-2-ethylthiophene

Base Information Edit
  • Chemical Name:4-Bromo-2-ethylthiophene
  • CAS No.:83663-40-5
  • Molecular Formula:C6H7BrS
  • Molecular Weight:191.092
  • Hs Code.:
  • Mol file:83663-40-5.mol
4-Bromo-2-ethylthiophene

Synonyms:4-Bromo-2-ethylthiophene

Suppliers and Price of 4-Bromo-2-ethylthiophene
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
  • CHESS?
  • KK002213:4-bromo-2-ethylthiophene 98
  • 1 g
  • $ 234.00
  • CHESS?
  • KK002213:4-bromo-2-ethylthiophene 98
  • 5 g
  • $ 720.00
  • Arctom
  • 4-Bromo-2-ethylthiophene 95%
  • 5g
  • $ 627.00
  • Arctom
  • 4-Bromo-2-ethylthiophene 95%
  • 1g
  • $ 341.00
Total 3 raw suppliers
Chemical Property of 4-Bromo-2-ethylthiophene Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

KK002213:4-bromo-2-ethylthiophene 98 *data from reagent suppliers

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

There total 5 articles about 4-Bromo-2-ethylthiophene 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:
2-bromo-5-ethylthiophene; With lithium diisopropyl amide; In tetrahydrofuran; at -70 ℃; for 2h; Inert atmosphere;
With methanol; In tetrahydrofuran; at -70 - 20 ℃; Inert atmosphere;
DOI:10.1039/c6md00128a
Guidance literature:
With potassium salt of hydrazide; hydrazine hydrate; In ethylene glycol; 1) 160 deg C, 0.5 h, 2) 160 deg C, 1 h.;
Guidance literature:
Multi-step reaction with 2 steps
1.1: acetic acid; N-Bromosuccinimide / chloroform / 3 h / 0 °C
2.1: lithium diisopropyl amide / tetrahydrofuran / 2 h / -70 °C / Inert atmosphere
2.2: 2 h / -70 °C
With N-Bromosuccinimide; acetic acid; lithium diisopropyl amide; In tetrahydrofuran; chloroform;
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