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Benzo[b]thiophen-5-ylmethanesulfonyl chloride

Base Information
  • Chemical Name:Benzo[b]thiophen-5-ylmethanesulfonyl chloride
  • CAS No.:128852-05-1
  • Molecular Formula:C8H5ClO2S2
  • Molecular Weight:232.711
  • Hs Code.:
  • Mol file:128852-05-1.mol
Benzo[b]thiophen-5-ylmethanesulfonyl chloride

Synonyms:BENZO[B]THIOPHEN-5-YLMETHANESULFONYL CHLORIDE;

Suppliers and Price of Benzo[b]thiophen-5-ylmethanesulfonyl chloride
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
  • Crysdot
  • Benzo[b]thiophene-5-sulfonylchloride 95+%
  • 1g
  • $ 510.00
  • Chemenu
  • benzo[b]thiophene-5-sulfonylchloride 95%
  • 1g
  • $ 482.00
  • American Custom Chemicals Corporation
  • BENZO[B]THIOPHENE-5-SULFONYL CHLORIDE 95.00%
  • 5MG
  • $ 504.83
  • Alichem
  • Benzo[b]thiophene-5-sulfonylchloride
  • 1g
  • $ 457.60
  • AK Scientific
  • Benzo[b]thiophene-5-sulfonylchloride
  • 1g
  • $ 728.00
Total 6 raw suppliers
Chemical Property of Benzo[b]thiophen-5-ylmethanesulfonyl chloride
Chemical Property:
  • PSA:70.76000 
  • LogP:4.05070 
  • Storage Temp.:2-8°C 
Purity/Quality:

97% *data from raw suppliers

Benzo[b]thiophene-5-sulfonylchloride 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Benzo[b]thiophen-5-ylmethanesulfonyl chloride

There total 1 articles about Benzo[b]thiophen-5-ylmethanesulfonyl chloride 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:
5-bromobenzo[b]thiophene; With tert.-butyl lithium; In diethyl ether; pentane; at -78 - 0 ℃;
With sulfur dioxide; In diethyl ether; pentane; at -78 - 20 ℃;
With N-chloro-succinimide; In diethyl ether; pentane;
DOI:10.1016/j.bmcl.2004.11.041
Guidance literature:
Multi-step reaction with 2 steps
1: aq. NH3 / acetone / 0 °C
2: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide*HCl; N,N-dimethylaminopyridine / CH2Cl2 / 20 °C
With dmap; ammonium hydroxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; acetone;
DOI:10.1016/j.bmcl.2004.11.041
Guidance literature:
Multi-step reaction with 4 steps
1: triethylamine / dichloromethane
2: potassium carbonate / N,N-dimethyl-formamide
3: hydrogenchloride; water / ethyl acetate
4: 4-methyl-morpholine; 2-chloro-1,3-dimethyl-2-imidazolinium hexafluorophosphate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane
With 4-methyl-morpholine; hydrogenchloride; water; potassium carbonate; 2-chloro-1,3-dimethyl-2-imidazolinium hexafluorophosphate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.08.087
upstream raw materials:

5-bromobenzo[b]thiophene

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