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Carbobenzyloxy-L-seryl-L-alanine benzyl ester

Base Information
  • Chemical Name:Carbobenzyloxy-L-seryl-L-alanine benzyl ester
  • CAS No.:6402-95-5
  • Molecular Formula:C21H24N2O6
  • Molecular Weight:400.431
  • Hs Code.:
  • European Community (EC) Number:667-955-9
  • Wikidata:Q76423161
Carbobenzyloxy-L-seryl-L-alanine benzyl ester

Synonyms:CARBOBENZYLOXY-L-SERYL-L-ALANINE BENZYL ESTER;AKOS024432443

Suppliers and Price of Carbobenzyloxy-L-seryl-L-alanine benzyl ester
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
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of Carbobenzyloxy-L-seryl-L-alanine benzyl ester
Chemical Property:
  • XLogP3:2
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:11
  • Exact Mass:400.16343649
  • Heavy Atom Count:29
  • Complexity:529
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C(=O)OCC1=CC=CC=C1)NC(=O)C(CO)NC(=O)OCC2=CC=CC=C2
  • Isomeric SMILES:C[C@@H](C(=O)OCC1=CC=CC=C1)NC(=O)[C@H](CO)NC(=O)OCC2=CC=CC=C2
Technology Process of Carbobenzyloxy-L-seryl-L-alanine benzyl ester

There total 3 articles about Carbobenzyloxy-L-seryl-L-alanine benzyl 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:
With 4-methyl-morpholine; In dichloromethane; at -15 ℃; for 1h;
DOI:10.1039/b509920j
Guidance literature:
Multi-step reaction with 2 steps
1: N-methyl morpholine / CH2Cl2 / 0.33 h / -15 °C
2: N-methyl morpholine / CH2Cl2 / -15 - 20 °C
With 4-methyl-morpholine; In dichloromethane;
DOI:10.1039/b515880j
Guidance literature:
With triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; acetonitrile;
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