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(S)-2-Benzyloxycarbonylamino-2-methyl-3-trityloxy-propionic acid methyl ester

Base Information
  • Chemical Name:(S)-2-Benzyloxycarbonylamino-2-methyl-3-trityloxy-propionic acid methyl ester
  • CAS No.:858132-50-0
  • Molecular Formula:C32H31NO5
  • Molecular Weight:509.602
  • Hs Code.:
(S)-2-Benzyloxycarbonylamino-2-methyl-3-trityloxy-propionic acid methyl ester

Synonyms:(S)-2-Benzyloxycarbonylamino-2-methyl-3-trityloxy-propionic acid methyl ester

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Chemical Property of (S)-2-Benzyloxycarbonylamino-2-methyl-3-trityloxy-propionic acid methyl ester
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Technology Process of (S)-2-Benzyloxycarbonylamino-2-methyl-3-trityloxy-propionic acid methyl ester

There total 8 articles about (S)-2-Benzyloxycarbonylamino-2-methyl-3-trityloxy-propionic acid 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:
With tert-butyl methyl ether; potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 4h;
DOI:10.1021/jo050407s
Guidance literature:
Multi-step reaction with 7 steps
1.1: dichloromethane / 0.5 h / 0 °C
2.1: carbon tetrabromide; triethylamine; triphenylphosphine / dichloromethane / 30 h / -10 °C
3.1: sodium hydride
3.2: molecular sieves 4 Angstroem / 13 / 1 h / 20 °C
4.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / methanol; acetone; tert-butyl alcohol / 3 h / 20 °C
5.1: sodium periodate / tetrahydrofuran; water / 2 h / 20 °C
6.1: sodium chlorite; potassium dihydrogenphosphate; 2-methyl-but-2-ene / water; tert-butyl alcohol / 0.5 h / 20 °C
7.1: tert-butyl methyl ether; potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C
With sodium chlorite; sodium periodate; potassium dihydrogenphosphate; osmium(VIII) oxide; 2-methyl-but-2-ene; tert-butyl methyl ether; carbon tetrabromide; sodium hydride; potassium carbonate; 4-methylmorpholine N-oxide; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; tert-butyl alcohol;
DOI:10.1021/jo050407s
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium hydride
1.2: molecular sieves 4 Angstroem / 13 / 1 h / 20 °C
2.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide / methanol; acetone; tert-butyl alcohol / 3 h / 20 °C
3.1: sodium periodate / tetrahydrofuran; water / 2 h / 20 °C
4.1: sodium chlorite; potassium dihydrogenphosphate; 2-methyl-but-2-ene / water; tert-butyl alcohol / 0.5 h / 20 °C
5.1: tert-butyl methyl ether; potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C
With sodium chlorite; sodium periodate; potassium dihydrogenphosphate; osmium(VIII) oxide; 2-methyl-but-2-ene; tert-butyl methyl ether; sodium hydride; potassium carbonate; 4-methylmorpholine N-oxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetone; tert-butyl alcohol;
DOI:10.1021/jo050407s
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