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(1R,5R)-9-benzyloxycarbonylamino-2-oxo-1-oxabicyclo[3.3.1]nonane

Base Information
  • Chemical Name:(1R,5R)-9-benzyloxycarbonylamino-2-oxo-1-oxabicyclo[3.3.1]nonane
  • CAS No.:1369774-33-3
  • Molecular Formula:C15H17NO4
  • Molecular Weight:275.304
  • Hs Code.:
(1R,5R)-9-benzyloxycarbonylamino-2-oxo-1-oxabicyclo[3.3.1]nonane

Synonyms:(1R,5R)-9-benzyloxycarbonylamino-2-oxo-1-oxabicyclo[3.3.1]nonane

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Chemical Property of (1R,5R)-9-benzyloxycarbonylamino-2-oxo-1-oxabicyclo[3.3.1]nonane
Chemical Property:
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Technology Process of (1R,5R)-9-benzyloxycarbonylamino-2-oxo-1-oxabicyclo[3.3.1]nonane

There total 7 articles about (1R,5R)-9-benzyloxycarbonylamino-2-oxo-1-oxabicyclo[3.3.1]nonane 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 2 steps
1: sodium hypochlorite; 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hydrogencarbonate; potassium bromide / water; acetone / 2.08 h / Cooling with ice
2: disodium hydrogenphosphate; 3-chloro-benzenecarboperoxoic acid / dichloromethane / 12 h / 20 °C
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; disodium hydrogenphosphate; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; potassium bromide; In dichloromethane; water; acetone; 2: Bayer-Villiger oxidation;
DOI:10.1039/c2ob06984a
Guidance literature:
Multi-step reaction with 5 steps
1: methanol / 20 °C
2: sodium hydroxide / dichloromethane; water
3: potassium carbonate / tetrahydrofuran / 16 h / 20 °C
4: sodium hypochlorite; 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hydrogencarbonate; potassium bromide / water; acetone / 2.08 h / Cooling with ice
5: disodium hydrogenphosphate; 3-chloro-benzenecarboperoxoic acid / dichloromethane / 12 h / 20 °C
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; disodium hydrogenphosphate; sodium hydrogencarbonate; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; potassium bromide; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; acetone; 5: Bayer-Villiger oxidation;
DOI:10.1039/c2ob06984a
Guidance literature:
Multi-step reaction with 4 steps
1: sodium hydroxide / dichloromethane; water
2: potassium carbonate / tetrahydrofuran / 16 h / 20 °C
3: sodium hypochlorite; 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hydrogencarbonate; potassium bromide / water; acetone / 2.08 h / Cooling with ice
4: disodium hydrogenphosphate; 3-chloro-benzenecarboperoxoic acid / dichloromethane / 12 h / 20 °C
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; disodium hydrogenphosphate; sodium hydrogencarbonate; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; potassium bromide; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; acetone; 4: Bayer-Villiger oxidation;
DOI:10.1039/c2ob06984a
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