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ethyl (1S,2S,3R,4S)-2-benzamido-3,4-dihydroxycyclopentanecarboxylate

Base Information Edit
  • Chemical Name:ethyl (1S,2S,3R,4S)-2-benzamido-3,4-dihydroxycyclopentanecarboxylate
  • CAS No.:1607805-68-4
  • Molecular Formula:C15H19NO5
  • Molecular Weight:293.32
  • Hs Code.:
  • Mol file:1607805-68-4.mol
ethyl (1S,2S,3R,4S)-2-benzamido-3,4-dihydroxycyclopentanecarboxylate

Synonyms:ethyl (1S,2S,3R,4S)-2-benzamido-3,4-dihydroxycyclopentanecarboxylate

Suppliers and Price of ethyl (1S,2S,3R,4S)-2-benzamido-3,4-dihydroxycyclopentanecarboxylate
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of ethyl (1S,2S,3R,4S)-2-benzamido-3,4-dihydroxycyclopentanecarboxylate Edit
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Technology Process of ethyl (1S,2S,3R,4S)-2-benzamido-3,4-dihydroxycyclopentanecarboxylate

There total 5 articles about ethyl (1S,2S,3R,4S)-2-benzamido-3,4-dihydroxycyclopentanecarboxylate 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 osmium(VIII) oxide; 4-methylmorpholine N-oxide; In acetone; at 20 ℃; for 8h;
DOI:10.1002/ejoc.201301281
Guidance literature:
Multi-step reaction with 4 steps
1: Candida antarctica lipase B; water / tert-butyl methyl ether / 4.5 h / 80 °C / Resolution of racemate; Enzymatic reaction
2: hydrogenchloride / 1 h / 0 °C
3: water; sodium hydroxide / toluene / 1 h / 0 °C
4: osmium(VIII) oxide; 4-methylmorpholine N-oxide / acetone / 8 h / 20 °C
With hydrogenchloride; Candida antarctica lipase B; osmium(VIII) oxide; water; 4-methylmorpholine N-oxide; sodium hydroxide; In tert-butyl methyl ether; acetone; toluene;
DOI:10.1002/ejoc.201301281
Guidance literature:
Multi-step reaction with 3 steps
1: hydrogenchloride / 1 h / 0 °C
2: water; sodium hydroxide / toluene / 1 h / 0 °C
3: osmium(VIII) oxide; 4-methylmorpholine N-oxide / acetone / 8 h / 20 °C
With hydrogenchloride; osmium(VIII) oxide; water; 4-methylmorpholine N-oxide; sodium hydroxide; In acetone; toluene;
DOI:10.1002/ejoc.201301281
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