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N-{N-[(3S)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl}-L-serine benzyl ester

Base Information
  • Chemical Name:N-{N-[(3S)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl}-L-serine benzyl ester
  • CAS No.:214406-40-3
  • Molecular Formula:C44H76N2O7
  • Molecular Weight:745.097
  • Hs Code.:
N-{N-[(3S)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl}-L-serine benzyl ester

Synonyms:N-{N-[(3S)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl}-L-serine benzyl ester

Suppliers and Price of N-{N-[(3S)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl}-L-serine benzyl ester
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-{N-[(3S)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl}-L-serine benzyl ester
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

Safty Information:
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MSDS Files:
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Technology Process of N-{N-[(3S)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl}-L-serine benzyl ester

There total 11 articles about N-{N-[(3S)-15-methyl-3-(13-methyltetradecanoyloxy)hexadecanoyl]glycyl}-L-serine 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:
Multi-step reaction with 4 steps
1: oxalyl chloride / CH2Cl2 / 1 h / Ambient temperature
2: Et3N / CH2Cl2 / 1 h / 0 - 5 °C
3: 94 percent / H2 / Pd/C / ethyl acetate / 2 h / Ambient temperature
4: 76 percent / DCC / CH2Cl2 / 2 h / Ambient temperature
With oxalyl dichloride; hydrogen; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1016/S0040-4020(98)83044-5
Guidance literature:
Multi-step reaction with 3 steps
1: Et3N / CH2Cl2 / 1 h / 0 - 5 °C
2: 94 percent / H2 / Pd/C / ethyl acetate / 2 h / Ambient temperature
3: 76 percent / DCC / CH2Cl2 / 2 h / Ambient temperature
With hydrogen; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1016/S0040-4020(98)83044-5
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