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Z-LYS(Z)-GLY-OH

Base Information
  • Chemical Name:Z-LYS(Z)-GLY-OH
  • CAS No.:37941-54-1
  • Molecular Formula:C24H29 N3 O7
  • Molecular Weight:471.5
  • Hs Code.:2924299090
  • Mol file:37941-54-1.mol
Z-LYS(Z)-GLY-OH

Synonyms:Glycine,N-(N2,N6-dicarboxy-L-lysyl)-, N2,N6-dibenzyl ester (6CI); Na,Ne-Dibenzyloxycarbonyl-L-lysylglycine

Suppliers and Price of Z-LYS(Z)-GLY-OH
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
  • TRC
  • Nα,Nε-Dibenzyloxycarbonyl-L-lysylglycine
  • 100mg
  • $ 1160.00
  • TRC
  • Nα,Nε-Dibenzyloxycarbonyl-L-lysylglycine
  • 50mg
  • $ 645.00
  • American Custom Chemicals Corporation
  • Z-LYS(Z)-GLY-OH 95.00%
  • 5MG
  • $ 499.73
Total 2 raw suppliers
Chemical Property of Z-LYS(Z)-GLY-OH
Chemical Property:
  • Melting Point:158-159 °C 
  • Boiling Point:780.2±60.0 °C(Predicted) 
  • PKA:3.41±0.10(Predicted) 
  • PSA:153.53000 
  • Density:1.262±0.06 g/cm3(Predicted) 
  • LogP:3.82800 
  • Storage Temp.:Store at 0°C 
  • Solubility.:DCM 
Purity/Quality:

98%Min *data from raw suppliers

Nα,Nε-Dibenzyloxycarbonyl-L-lysylglycine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Nα,Nε-Dibenzyloxycarbonyl-L-lysylglycine intermediate in the synthesis of Avizfone (A794685), the prodrug to Diazepam (D416855), a compound used to treat organophosphate poisoning.
Technology Process of Z-LYS(Z)-GLY-OH

There total 7 articles about Z-LYS(Z)-GLY-OH 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 sodium hydroxide; In methanol; at 0 ℃; for 4h;
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) N-methylmorpholine, ethyl chloroformate, 2.) N-methylmorpholine / 1.) THF, -15 deg C, 15 min, 2.) THF, CHCl3, 0 deg C, 1 h; room temp., overnight
2: 90 percent / 1 N NaOH / methanol / 4 h / 0 °C
With 4-methyl-morpholine; sodium hydroxide; chloroformic acid ethyl ester; In methanol;
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