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Tert-butyl phenylsulfonylcarbamate

Base Information Edit
  • Chemical Name:Tert-butyl phenylsulfonylcarbamate
  • CAS No.:2845-66-1
  • Molecular Formula:C11H15NO4S
  • Molecular Weight:257.31
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80477993
  • Nikkaji Number:J3.445.117F
  • Mol file:2845-66-1.mol
Tert-butyl phenylsulfonylcarbamate

Synonyms:2845-66-1;tert-butyl phenylsulfonylcarbamate;SCHEMBL5394506;DTXSID80477993;tert-Butyl (benzenesulfonyl)carbamate;TERT-BUTYL N-(BENZENESULFONYL)CARBAMATE;EN300-12463991;Z1508686583

Suppliers and Price of Tert-butyl phenylsulfonylcarbamate
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 7 raw suppliers
Chemical Property of Tert-butyl phenylsulfonylcarbamate Edit
Chemical Property:
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:257.07217913
  • Heavy Atom Count:17
  • Complexity:358
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NS(=O)(=O)C1=CC=CC=C1
Technology Process of Tert-butyl phenylsulfonylcarbamate

There total 5 articles about Tert-butyl phenylsulfonylcarbamate 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 dmap; triethylamine; In dichloromethane; at 20 ℃; for 3h; under 760.051 Torr;
DOI:10.1021/acs.orglett.7b00879
Guidance literature:
In tetrahydrofuran; at 0 ℃; Inert atmosphere;
DOI:10.1021/acs.joc.5b01287
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