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methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate

Base Information Edit
  • Chemical Name:methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate
  • CAS No.:220652-54-0
  • Molecular Formula:C21H21NO5
  • Molecular Weight:367.401
  • Hs Code.:
  • Mol file:220652-54-0.mol
methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate

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Suppliers and Price of methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate Edit
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Technology Process of methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate

There total 5 articles about methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate 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: 1.) n-BuLi, 3.) (+)-(camphorsulfonyloxaziridine / 1.) hexane, -78 deg C, 1 h, 2.) THF, -78 deg C, 1 h, 3.) -78 deg C, 6 h; warm to room temperature
2: 93 percent / Pd(PPh3)4, N,N'-dimethylbarbituric acid / CH2Cl2 / Ambient temperature
3: 201 g / Et3N / tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, overnight
4: 98 percent formic acid / 3 h / 60 °C
5: SOCl2, Et3N / 2.5 h / Heating
With tetrakis(triphenylphosphine) palladium(0); n-butyllithium; formic acid; thionyl chloride; 1,3-dimethylbarbituric acid; (1S)-(+)-(10-camphorsulfonyl)-oxaziridine; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(98)01051-5
Guidance literature:
Multi-step reaction with 3 steps
1: 201 g / Et3N / tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, overnight
2: 98 percent formic acid / 3 h / 60 °C
3: SOCl2, Et3N / 2.5 h / Heating
With formic acid; thionyl chloride; triethylamine; In tetrahydrofuran;
DOI:10.1016/S0040-4020(98)01051-5
Guidance literature:
Multi-step reaction with 4 steps
1: 93 percent / Pd(PPh3)4, N,N'-dimethylbarbituric acid / CH2Cl2 / Ambient temperature
2: 201 g / Et3N / tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, overnight
3: 98 percent formic acid / 3 h / 60 °C
4: SOCl2, Et3N / 2.5 h / Heating
With tetrakis(triphenylphosphine) palladium(0); formic acid; thionyl chloride; 1,3-dimethylbarbituric acid; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(98)01051-5
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