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(3S,4R)-allyl 3-(tert-butyldimethylsiloxy)-4-{(S)-2-[(R)-2-[(S,E)-3-(4-methoxybenzyloxy)-7-(tritylthio)hept-4-enoylamino]propionylamino]-3-tritylthio(propionylamino)}-6-methylheptanoate

Base Information
  • Chemical Name:(3S,4R)-allyl 3-(tert-butyldimethylsiloxy)-4-{(S)-2-[(R)-2-[(S,E)-3-(4-methoxybenzyloxy)-7-(tritylthio)hept-4-enoylamino]propionylamino]-3-tritylthio(propionylamino)}-6-methylheptanoate
  • CAS No.:1426828-70-7
  • Molecular Formula:C76H91N3O8S2Si
  • Molecular Weight:1266.79
  • Hs Code.:
(3S,4R)-allyl 3-(tert-butyldimethylsiloxy)-4-{(S)-2-[(R)-2-[(S,E)-3-(4-methoxybenzyloxy)-7-(tritylthio)hept-4-enoylamino]propionylamino]-3-tritylthio(propionylamino)}-6-methylheptanoate

Synonyms:(3S,4R)-allyl 3-(tert-butyldimethylsiloxy)-4-{(S)-2-[(R)-2-[(S,E)-3-(4-methoxybenzyloxy)-7-(tritylthio)hept-4-enoylamino]propionylamino]-3-tritylthio(propionylamino)}-6-methylheptanoate

Suppliers and Price of (3S,4R)-allyl 3-(tert-butyldimethylsiloxy)-4-{(S)-2-[(R)-2-[(S,E)-3-(4-methoxybenzyloxy)-7-(tritylthio)hept-4-enoylamino]propionylamino]-3-tritylthio(propionylamino)}-6-methylheptanoate
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Chemical Property of (3S,4R)-allyl 3-(tert-butyldimethylsiloxy)-4-{(S)-2-[(R)-2-[(S,E)-3-(4-methoxybenzyloxy)-7-(tritylthio)hept-4-enoylamino]propionylamino]-3-tritylthio(propionylamino)}-6-methylheptanoate
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Technology Process of (3S,4R)-allyl 3-(tert-butyldimethylsiloxy)-4-{(S)-2-[(R)-2-[(S,E)-3-(4-methoxybenzyloxy)-7-(tritylthio)hept-4-enoylamino]propionylamino]-3-tritylthio(propionylamino)}-6-methylheptanoate

There total 10 articles about (3S,4R)-allyl 3-(tert-butyldimethylsiloxy)-4-{(S)-2-[(R)-2-[(S,E)-3-(4-methoxybenzyloxy)-7-(tritylthio)hept-4-enoylamino]propionylamino]-3-tritylthio(propionylamino)}-6-methylheptanoate 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 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; at -30 ℃; for 3h; Inert atmosphere;
DOI:10.1016/j.ejmech.2012.12.023
Guidance literature:
Multi-step reaction with 7 steps
1.1: lithium diisopropyl amide / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere
1.2: 0.67 h / -78 °C / Inert atmosphere
2.1: 1H-imidazole / N,N-dimethyl-formamide / 24 h / 20 °C
3.1: sodium hydroxide / ethanol / 6 h / 20 °C
4.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 20 °C
5.1: trimethylsilyl trifluoromethanesulfonate; 2,6-dimethylpyridine / dichloromethane / 1 h / 20 °C
5.2: 1 h / 0 - 20 °C
6.1: trimethylsilyl trifluoromethanesulfonate; 2,6-dimethylpyridine / dichloromethane / 1 h / 20 °C
6.2: 1 h / 0 - 20 °C
7.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; 1-hydroxy-7-aza-benzotriazole / dichloromethane / 3 h / -30 °C / Inert atmosphere
With 1H-imidazole; 2,6-dimethylpyridine; 1-hydroxy-7-aza-benzotriazole; trimethylsilyl trifluoromethanesulfonate; potassium carbonate; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.12.023
Guidance literature:
Multi-step reaction with 7 steps
1.1: potassium borohydride / methanol / 5 h / -40 °C
2.1: 1H-imidazole / N,N-dimethyl-formamide / 24 h / 20 °C
3.1: sodium hydroxide / ethanol / 6 h / 20 °C
4.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 20 °C
5.1: trimethylsilyl trifluoromethanesulfonate; 2,6-dimethylpyridine / dichloromethane / 1 h / 20 °C
5.2: 1 h / 0 - 20 °C
6.1: trimethylsilyl trifluoromethanesulfonate; 2,6-dimethylpyridine / dichloromethane / 1 h / 20 °C
6.2: 1 h / 0 - 20 °C
7.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; 1-hydroxy-7-aza-benzotriazole / dichloromethane / 3 h / -30 °C / Inert atmosphere
With 1H-imidazole; 2,6-dimethylpyridine; 1-hydroxy-7-aza-benzotriazole; potassium borohydride; trimethylsilyl trifluoromethanesulfonate; potassium carbonate; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium hydroxide; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.12.023
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