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L-Isoleucine, N-[N-[1-[1-[N-[1-[N-[N-[(phenylmethoxy)carbonyl]-L-valyl]-L-tyrosyl]-L-prol yl]-L-phenylalanyl]-L-prolyl]-L-prolyl]glycyl]-, phenylmethyl ester

Base Information Edit
  • Chemical Name:L-Isoleucine, N-[N-[1-[1-[N-[1-[N-[N-[(phenylmethoxy)carbonyl]-L-valyl]-L-tyrosyl]-L-prol yl]-L-phenylalanyl]-L-prolyl]-L-prolyl]glycyl]-, phenylmethyl ester
  • CAS No.:90315-58-5
  • Molecular Formula:C61H76N8O12
  • Molecular Weight:1113.32
  • Hs Code.:
  • Mol file:90315-58-5.mol
L-Isoleucine,
N-[N-[1-[1-[N-[1-[N-[N-[(phenylmethoxy)carbonyl]-L-valyl]-L-tyrosyl]-L-prol
yl]-L-phenylalanyl]-L-prolyl]-L-prolyl]glycyl]-, phenylmethyl ester

Synonyms:

Suppliers and Price of L-Isoleucine, N-[N-[1-[1-[N-[1-[N-[N-[(phenylmethoxy)carbonyl]-L-valyl]-L-tyrosyl]-L-prol yl]-L-phenylalanyl]-L-prolyl]-L-prolyl]glycyl]-, phenylmethyl ester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of L-Isoleucine, N-[N-[1-[1-[N-[1-[N-[N-[(phenylmethoxy)carbonyl]-L-valyl]-L-tyrosyl]-L-prol yl]-L-phenylalanyl]-L-prolyl]-L-prolyl]glycyl]-, phenylmethyl ester Edit
Chemical Property:
Purity/Quality:
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Technology Process of L-Isoleucine, N-[N-[1-[1-[N-[1-[N-[N-[(phenylmethoxy)carbonyl]-L-valyl]-L-tyrosyl]-L-prol yl]-L-phenylalanyl]-L-prolyl]-L-prolyl]glycyl]-, phenylmethyl ester

There total 13 articles about L-Isoleucine, N-[N-[1-[1-[N-[1-[N-[N-[(phenylmethoxy)carbonyl]-L-valyl]-L-tyrosyl]-L-prol yl]-L-phenylalanyl]-L-prolyl]-L-prolyl]glycyl]-, phenylmethyl 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 5 steps
1: NMM, DCC / acetonitrile, 0 deg C, overnight
2: 60 percent / H2 / Pd black / methanol
3: 1) NMM, ECF, 2) NMM
4: 83 percent / 4 M hydrogen chloride / dioxane
5: DCC, NMM, HOBt
With 4-methyl-morpholine; hydrogenchloride; hydrogen; chloroformic acid ethyl ester; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium; In 1,4-dioxane; methanol;
DOI:10.1246/bcsj.57.97
Guidance literature:
Multi-step reaction with 5 steps
1: NMM, DCC / acetonitrile, 0 deg C, overnight
2: 60 percent / H2 / Pd black / methanol
3: 1) NMM, ECF, 2) NMM
4: 83 percent / 4 M hydrogen chloride / dioxane
5: DCC, NMM, HOBt
With 4-methyl-morpholine; hydrogenchloride; hydrogen; chloroformic acid ethyl ester; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium; In 1,4-dioxane; methanol;
DOI:10.1246/bcsj.57.97
Guidance literature:
Multi-step reaction with 4 steps
1: 94 percent / H2, 0.3 M hydrogen chloride / Pd black / methanol
2: NMM, HOBt, DCC / THF, 0 deg C, overnight
3: 70 percent / 2 m NaOH / methanol
4: DCC, NMM, HOBt
With 4-methyl-morpholine; hydrogenchloride; sodium hydroxide; hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium; In methanol;
DOI:10.1246/bcsj.57.97
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