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L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-(4-methyl-5-oxo-2-thioxo-1-imid azolidinyl)-, methyl ester

Base Information Edit
  • Chemical Name:L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-(4-methyl-5-oxo-2-thioxo-1-imid azolidinyl)-, methyl ester
  • CAS No.:95753-62-1
  • Molecular Formula:C29H27N3O5S
  • Molecular Weight:529.616
  • Hs Code.:
  • Mol file:95753-62-1.mol
L-Phenylalanine,
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-(4-methyl-5-oxo-2-thioxo-1-imid
azolidinyl)-, methyl ester

Synonyms:

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Chemical Property of L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-(4-methyl-5-oxo-2-thioxo-1-imid azolidinyl)-, methyl ester Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
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MSDS Files:
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Technology Process of L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-(4-methyl-5-oxo-2-thioxo-1-imid azolidinyl)-, methyl ester

There total 9 articles about L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-(4-methyl-5-oxo-2-thioxo-1-imid azolidinyl)-, methyl 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: 90 percent / H2 / 10percent Pd-C / dioxane / 1 h / Ambient temperature
2: SOCl2
3: 79 percent / 1 M NaHCO3 / CHCl3; H2O / 2 h / Ambient temperature
4: 1.) Et3N / 1.) pyridine, dioxane, H2O, 40 deg C, 2 h; 2.) trifluoroacetic acid, Rt, 30 min
With thionyl chloride; hydrogen; sodium hydrogencarbonate; triethylamine; palladium on activated charcoal; In 1,4-dioxane; chloroform; water;
DOI:10.1039/P29840001723
Guidance literature:
Multi-step reaction with 4 steps
1: 90 percent / H2 / 10percent Pd-C / dioxane / 1 h / Ambient temperature
2: SOCl2
3: 79 percent / 1 M NaHCO3 / CHCl3; H2O / 2 h / Ambient temperature
4: 1.) NaHCO3 / 1.) pyridine, dioxan, H2O, Rt, 1 h; 2.) trifluoroacetic acid, Rt, 1 h
With thionyl chloride; hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In 1,4-dioxane; chloroform; water;
DOI:10.1039/P29840001723
Guidance literature:
Multi-step reaction with 3 steps
1: SOCl2
2: 79 percent / 1 M NaHCO3 / CHCl3; H2O / 2 h / Ambient temperature
3: 1.) Et3N / 1.) pyridine, dioxane, H2O, 40 deg C, 2 h; 2.) trifluoroacetic acid, Rt, 30 min
With thionyl chloride; sodium hydrogencarbonate; triethylamine; In chloroform; water;
DOI:10.1039/P29840001723
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