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L-Glutamine, N-(2-oxo-3-piperidinyl)-N2-(1-oxopropyl)-, ethyl ester, ( S)-

Base Information Edit
  • Chemical Name:L-Glutamine, N-(2-oxo-3-piperidinyl)-N2-(1-oxopropyl)-, ethyl ester, ( S)-
  • CAS No.:84563-47-3
  • Molecular Formula:C15H25N3O5
  • Molecular Weight:327.381
  • Hs Code.:2933790090
  • Mol file:84563-47-3.mol
L-Glutamine, N-(2-oxo-3-piperidinyl)-N2-(1-oxopropyl)-, ethyl ester, ( S)-

Synonyms:L-Glutamine,N-(2-oxo-3-piperidinyl)-N2-(1-oxopropyl)-, ethyl ester, (S)-; Glorin

Suppliers and Price of L-Glutamine, N-(2-oxo-3-piperidinyl)-N2-(1-oxopropyl)-, ethyl ester, ( S)-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of L-Glutamine, N-(2-oxo-3-piperidinyl)-N2-(1-oxopropyl)-, ethyl ester, ( S)- Edit
Chemical Property:
  • Vapor Pressure:2.93E-16mmHg at 25°C 
  • Boiling Point:639.7°C at 760 mmHg 
  • Flash Point:340.7°C 
  • PSA:123.28000 
  • Density:1.21g/cm3 
  • LogP:1.12640 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of L-Glutamine, N-(2-oxo-3-piperidinyl)-N2-(1-oxopropyl)-, ethyl ester, ( S)-

There total 10 articles about L-Glutamine, N-(2-oxo-3-piperidinyl)-N2-(1-oxopropyl)-, ethyl ester, ( S)- 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; isobutyl chloroformate; In N,N-dimethyl-formamide; at -10 ℃; for 0.0833333h;
Guidance literature:
With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 2h; under 760.051 Torr;
DOI:10.3762/bjoc.13.27
Guidance literature:
Multi-step reaction with 4 steps
1: 71 percent / NaHCO3 / dioxane; H2O / 2 h / Ambient temperature
2: 85 percent / dicyclohexylcarboimide, 4-(dimethylamino)pyridine / CH2Cl2 / Ambient temperature
3: 90 percent / ammonium formate / 10 percent Pd/C / methanol / 0.25 h / Ambient temperature
4: 75 percent / N-methylmorpholine, isobutyl chloroformate / dimethylformamide / 0.08 h / -10 °C
With 4-methyl-morpholine; dmap; ammonium formate; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; isobutyl chloroformate; palladium on activated charcoal; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;
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