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N-Benzyloxycarbonyl-L-glutamic anhydride

Base Information
  • Chemical Name:N-Benzyloxycarbonyl-L-glutamic anhydride
  • CAS No.:84668-91-7
  • Molecular Formula:C13H13NO5
  • Molecular Weight:263.24600
  • Hs Code.:
  • European Community (EC) Number:223-930-0,622-072-8
  • DSSTox Substance ID:DTXSID10961517
  • Mol file:84668-91-7.mol
N-Benzyloxycarbonyl-L-glutamic anhydride

Synonyms:N-Benzyloxycarbonyl-L-glutamic anhydride;benzyl N-(2,6-dioxooxan-3-yl)carbamate;4124-76-9;[(3R)-Tetrahydro-2,6-dioxo-2H-pyran-3-yl]-carbamic Acid Phenylmethyl;EINECS 223-930-0;SCHEMBL6794132;DTXSID10961517;carbobenzyloxy-l-glutamic anhydride;AKOS024332814;FT-0674994;Benzyl hydrogen (2,6-dioxooxan-3-yl)carbonimidate

Suppliers and Price of N-Benzyloxycarbonyl-L-glutamic anhydride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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  • price
Total 3 raw suppliers
Chemical Property of N-Benzyloxycarbonyl-L-glutamic anhydride
Chemical Property:
  • Melting Point:103 - 105 °C 
  • PSA:81.70000 
  • LogP:1.53590 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:263.07937252
  • Heavy Atom Count:19
  • Complexity:362
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CC(=O)OC(=O)C1NC(=O)OCC2=CC=CC=C2
Technology Process of N-Benzyloxycarbonyl-L-glutamic anhydride

There total 5 articles about N-Benzyloxycarbonyl-L-glutamic anhydride 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 dicyclohexyl-carbodiimide; In ethyl acetate; 1.) 1 h, 0 deg C, 2.) 24 h, r.t.;
DOI:10.1246/bcsj.62.2748
Guidance literature:
Multi-step reaction with 2 steps
1: 72 percent
2: 96 percent / dicyclohexylcarbodiimide / ethyl acetate / 1.) 1 h, 0 deg C, 2.) 24 h, r.t.
With dicyclohexyl-carbodiimide; In ethyl acetate;
DOI:10.1246/bcsj.62.2748
Guidance literature:
Multi-step reaction with 2 steps
1: 72 percent
2: 96 percent / dicyclohexylcarbodiimide / ethyl acetate / 1.) 1 h, 0 deg C, 2.) 24 h, r.t.
With dicyclohexyl-carbodiimide; In ethyl acetate;
DOI:10.1246/bcsj.62.2748
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