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indol-5-ylsulfonyl chloride

Base Information Edit
  • Chemical Name:indol-5-ylsulfonyl chloride
  • CAS No.:1094209-33-2
  • Molecular Formula:C8H6ClNO2S
  • Molecular Weight:215.66
  • Hs Code.:
  • Mol file:1094209-33-2.mol
indol-5-ylsulfonyl chloride

Synonyms:indol-5-ylsulfonyl chloride;1H‐indole‐5‐sulfonyl chloride

Suppliers and Price of indol-5-ylsulfonyl chloride
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
  • TRC
  • 1H-Indole-5-sulfonylChloride
  • 250mg
  • $ 220.00
  • Crysdot
  • 1H-Indole-5-sulfonylchloride 95+%
  • 1g
  • $ 766.00
  • Crysdot
  • 1H-Indole-5-sulfonylchloride 95+%
  • 5g
  • $ 2306.00
  • Chemenu
  • 1H-Indole-5-sulfonylchloride 95%
  • 5g
  • $ 2173.00
  • Chemenu
  • 1H-Indole-5-sulfonylchloride 95%
  • 1g
  • $ 724.00
  • ACHEMBLOCK
  • 1H-Indole-5-sulfonylchloride 97%
  • 250MG
  • $ 298.00
Total 14 raw suppliers
Chemical Property of indol-5-ylsulfonyl chloride Edit
Chemical Property:
  • PSA:58.31000 
  • LogP:3.17620 
Purity/Quality:

97% *data from raw suppliers

1H-Indole-5-sulfonylChloride *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 1H-Indole-5-sulfonyl Chloride is being used as a reagent in the preparation of sulphonamide derivatives of benzylamine for the treatment of CNS diseases.
Technology Process of indol-5-ylsulfonyl chloride

There total 1 articles about indol-5-ylsulfonyl 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-bromo-1H-indole; With n-butyllithium; In diethyl ether; at -78 ℃; for 0.666667h;
With sulfur dioxide; In diethyl ether; at -78 - 20 ℃;
With N-chloro-succinimide; In diethyl ether; at 20 ℃; for 1.5h;
Guidance literature:
With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; for 16h; Inert atmosphere;
upstream raw materials:

5-bromo-1H-indole

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