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L-Glutamic acid, N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-, 1-[(2,6-dichlorophenyl)methyl] 5-hexadecyl ester

Base Information
  • Chemical Name:L-Glutamic acid, N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-, 1-[(2,6-dichlorophenyl)methyl] 5-hexadecyl ester
  • CAS No.:88887-48-3
  • Molecular Formula:C43H58Cl2N8O5
  • Molecular Weight:837.89
  • Hs Code.:
L-Glutamic acid,
N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-,
1-[(2,6-dichlorophenyl)methyl] 5-hexadecyl ester

Synonyms:

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Chemical Property of L-Glutamic acid, N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-, 1-[(2,6-dichlorophenyl)methyl] 5-hexadecyl ester
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of L-Glutamic acid, N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-, 1-[(2,6-dichlorophenyl)methyl] 5-hexadecyl ester

There total 9 articles about L-Glutamic acid, N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-, 1-[(2,6-dichlorophenyl)methyl] 5-hexadecyl 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:
Multi-step reaction with 7 steps
1: 96 percent / Cs2CO2 / dimethylformamide / 60 h / Ambient temperature
2: 92 percent / H2 / 5percent Pd/C / propan-2-ol / 1520 - 2280 Torr / Ambient temperature
3: 100 percent / DCC, pyridine / acetonitrile; dimethylformamide / 1 h / 0 °C
4: 100 percent / benzene / 1 h / Heating
5: 1.) diethyl phosphorocyanidate, Et3N / 1.) DMF, 80 deg C, 2 min, 2.) DMF, 80 deg C, 2 h
6: 53 percent / tetrabutylammonium chloride, KF*2H2O / acetonitrile; dimethylformamide / 48 h / 48 °C
7: 18 percent / Na2CO3 / dimethylformamide / 2.5 h / Ambient temperature
With pyridine; potassium fluoride; diethyl cyanophosphonate; tetrabutyl-ammonium chloride; hydrogen; sodium carbonate; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In N,N-dimethyl-formamide; isopropyl alcohol; acetonitrile; benzene;
DOI:10.1021/jm00371a009
Guidance literature:
Multi-step reaction with 7 steps
1: 96 percent / Cs2CO2 / dimethylformamide / 60 h / Ambient temperature
2: 92 percent / H2 / 5percent Pd/C / propan-2-ol / 1520 - 2280 Torr / Ambient temperature
3: 100 percent / DCC, pyridine / acetonitrile; dimethylformamide / 1 h / 0 °C
4: 100 percent / benzene / 1 h / Heating
5: 1.) diethyl phosphorocyanidate, Et3N / 1.) DMF, 80 deg C, 2 min, 2.) DMF, 80 deg C, 2 h
6: 53 percent / tetrabutylammonium chloride, KF*2H2O / acetonitrile; dimethylformamide / 48 h / 48 °C
7: 18 percent / Na2CO3 / dimethylformamide / 2.5 h / Ambient temperature
With pyridine; potassium fluoride; diethyl cyanophosphonate; tetrabutyl-ammonium chloride; hydrogen; sodium carbonate; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In N,N-dimethyl-formamide; isopropyl alcohol; acetonitrile; benzene;
DOI:10.1021/jm00371a009
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