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Carbamic acid, [(4-methylphenyl)sulfonyl]-, 2-propynyl ester

Base Information
  • Chemical Name:Carbamic acid, [(4-methylphenyl)sulfonyl]-, 2-propynyl ester
  • CAS No.:63924-66-3
  • Molecular Formula:C11H11NO4S
  • Molecular Weight:253.279
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50453542
  • Nikkaji Number:J1.403.672E
  • Wikidata:Q82274698
Carbamic acid, [(4-methylphenyl)sulfonyl]-, 2-propynyl ester

Synonyms:63924-66-3;Carbamic acid, [(4-methylphenyl)sulfonyl]-, 2-propynyl ester;DTXSID50453542;Tosylcarbamic acid propargyl ester

Suppliers and Price of Carbamic acid, [(4-methylphenyl)sulfonyl]-, 2-propynyl ester
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Chemical Property of Carbamic acid, [(4-methylphenyl)sulfonyl]-, 2-propynyl ester
Chemical Property:
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:253.04087901
  • Heavy Atom Count:17
  • Complexity:407
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC(=O)OCC#C
Technology Process of Carbamic acid, [(4-methylphenyl)sulfonyl]-, 2-propynyl ester

There total 2 articles about Carbamic acid, [(4-methylphenyl)sulfonyl]-, 2-propynyl ester 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:
In tetrahydrofuran; at 20 ℃; for 0.166667h;
DOI:10.1021/jo070681h
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium dichloride; at 75 ℃; for 20h;
DOI:10.1021/acs.joc.5b02755
Guidance literature:
With sodium acetate; In acetone; at 20 ℃; for 0.333333h; Reagent/catalyst; Solvent; Catalytic behavior;
DOI:10.1002/chem.201900678
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