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PHENYLSULFONYLMETHYL ISOCYANIDE

Base Information Edit
  • Chemical Name:PHENYLSULFONYLMETHYL ISOCYANIDE
  • CAS No.:36635-63-9
  • Molecular Formula:C8H7 N O2 S
  • Molecular Weight:181.215
  • Hs Code.:2926909090
  • Mol file:36635-63-9.mol
PHENYLSULFONYLMETHYL ISOCYANIDE

Synonyms:Phenylsulfonylmethylisocyanide

Suppliers and Price of PHENYLSULFONYLMETHYL ISOCYANIDE
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
Total 2 raw suppliers
Chemical Property of PHENYLSULFONYLMETHYL ISOCYANIDE Edit
Chemical Property:
  • PSA:42.52000 
  • LogP:1.64860 
Purity/Quality:

98% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of PHENYLSULFONYLMETHYL ISOCYANIDE

There total 5 articles about PHENYLSULFONYLMETHYL ISOCYANIDE 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 diisopropylamine; trichlorophosphate; In tetrahydrofuran; acetonitrile; at -20 - 5 ℃; for 1h; Inert atmosphere;
DOI:10.1002/ejoc.201403615
Guidance literature:
Multi-step reaction with 2 steps
1: formic acid; toluene / 3 h / 100 °C / Inert atmosphere; Microwave irradiation
2: diisopropylamine; trichlorophosphate / tetrahydrofuran; acetonitrile / 1 h / -20 - 5 °C / Inert atmosphere
With diisopropylamine; trichlorophosphate; In tetrahydrofuran; formic acid; toluene; acetonitrile;
DOI:10.1002/ejoc.201403615
Guidance literature:
Multi-step reaction with 3 steps
1: N-Bromosuccinimide / dichloromethane / 1 h / 0 °C
2: formic acid; toluene / 3 h / 100 °C / Inert atmosphere; Microwave irradiation
3: diisopropylamine; trichlorophosphate / tetrahydrofuran; acetonitrile / 1 h / -20 - 5 °C / Inert atmosphere
With N-Bromosuccinimide; diisopropylamine; trichlorophosphate; In tetrahydrofuran; formic acid; dichloromethane; toluene; acetonitrile;
DOI:10.1002/ejoc.201403615
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