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Ethyl 2-phenylprop-2-en-1-yl carbonate

Base Information
  • Chemical Name:Ethyl 2-phenylprop-2-en-1-yl carbonate
  • CAS No.:86537-63-5
  • Molecular Formula:C12H14O3
  • Molecular Weight:206.241
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20524091
  • Wikidata:Q82390703
Ethyl 2-phenylprop-2-en-1-yl carbonate

Synonyms:86537-63-5;Ethyl 2-phenylprop-2-en-1-yl carbonate;DTXSID20524091

Suppliers and Price of Ethyl 2-phenylprop-2-en-1-yl carbonate
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Ethyl 2-phenylprop-2-en-1-yl carbonate
Chemical Property:
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:6
  • Exact Mass:206.094294304
  • Heavy Atom Count:15
  • Complexity:217
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)OCC(=C)C1=CC=CC=C1
Technology Process of Ethyl 2-phenylprop-2-en-1-yl carbonate

There total 1 articles about Ethyl 2-phenylprop-2-en-1-yl carbonate 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 pyridine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/acs.orglett.9b01497
Guidance literature:
tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine; In tetrahydrofuran; at 50 ℃; for 2h; further Pd catalyst;
DOI:10.1016/0040-4039(90)87025-U
Guidance literature:
tert-butyl ((S)-2-hydroxy-3-phenylpropionylamino)acetate; With triisopropoxytitanium(IV) chloride; In tetrahydrofuran; hexane; at 20 ℃; for 0.333333h; Schlenk technique;
With n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; at -78 - 20 ℃; Schlenk technique;
Ethyl 2-Phenyl-2-propenyl carbonate; With bis(η3-allyl-μ-chloropalladium(II)); triphenylphosphine; In tetrahydrofuran; at -78 - 20 ℃; stereoselective reaction; Schlenk technique;
DOI:10.1021/acs.orglett.9b01497
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