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2-<3-benzyl-6-oxo-2-thia-4,7-diaza-(1R,5R)-bicyclo-<3.2.0>-hept-3-en-7-yl>-mono-benzhydryl malonate

Base Information Edit
  • Chemical Name:2-<3-benzyl-6-oxo-2-thia-4,7-diaza-(1R,5R)-bicyclo-<3.2.0>-hept-3-en-7-yl>-mono-benzhydryl malonate
  • CAS No.:78815-19-7
  • Molecular Formula:C27H22N2O5S
  • Molecular Weight:486.548
  • Hs Code.:
  • Mol file:78815-19-7.mol
2-<3-benzyl-6-oxo-2-thia-4,7-diaza-(1R,5R)-bicyclo-<3.2.0>-hept-3-en-7-yl>-mono-benzhydryl malonate

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-<3-benzyl-6-oxo-2-thia-4,7-diaza-(1R,5R)-bicyclo-<3.2.0>-hept-3-en-7-yl>-mono-benzhydryl malonate Edit
Chemical Property:
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Technology Process of 2-<3-benzyl-6-oxo-2-thia-4,7-diaza-(1R,5R)-bicyclo-<3.2.0>-hept-3-en-7-yl>-mono-benzhydryl malonate

There total 5 articles about 2-<3-benzyl-6-oxo-2-thia-4,7-diaza-(1R,5R)-bicyclo-<3.2.0>-hept-3-en-7-yl>-mono-benzhydryl malonate 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) NaIO4 / 1) H2O; 2) NEt3, DMF, 20 deg C
2: 65 percent Chromat. / MgSO4, (CH3O)3P / benzene / 40 h / Heating
3: 74 percent / KMnO4, MgSO4 / H2O; ethanol / 15 - 20 °C
4: 1) Triton B / 1) DMF, CH3OH, -30 deg C, 15 min; 0 deg C, 15 min; 2) DMF, 15 min, -30 deg C; 1 h, 0 deg C; 2 h, r. t.
5: 1) lithium hexamethyldisilazide-ether 1:1 complex / 1) THF, -60 deg C, 30 min; 2) -60 deg C, 30 min, without cooling, 1 h
With potassium permanganate; sodium periodate; N-benzyl-trimethylammonium hydroxide; magnesium sulfate; lithium hexamethyldisilazane; phosphorous acid trimethyl ester; In ethanol; water; benzene;
DOI:10.1016/S0040-4020(01)92143-X
Guidance literature:
Multi-step reaction with 4 steps
1: 65 percent Chromat. / MgSO4, (CH3O)3P / benzene / 40 h / Heating
2: 74 percent / KMnO4, MgSO4 / H2O; ethanol / 15 - 20 °C
3: 1) Triton B / 1) DMF, CH3OH, -30 deg C, 15 min; 0 deg C, 15 min; 2) DMF, 15 min, -30 deg C; 1 h, 0 deg C; 2 h, r. t.
4: 1) lithium hexamethyldisilazide-ether 1:1 complex / 1) THF, -60 deg C, 30 min; 2) -60 deg C, 30 min, without cooling, 1 h
With potassium permanganate; N-benzyl-trimethylammonium hydroxide; magnesium sulfate; lithium hexamethyldisilazane; phosphorous acid trimethyl ester; In ethanol; water; benzene;
DOI:10.1016/S0040-4020(01)92143-X
Guidance literature:
Multi-step reaction with 3 steps
1: 74 percent / KMnO4, MgSO4 / H2O; ethanol / 15 - 20 °C
2: 1) Triton B / 1) DMF, CH3OH, -30 deg C, 15 min; 0 deg C, 15 min; 2) DMF, 15 min, -30 deg C; 1 h, 0 deg C; 2 h, r. t.
3: 1) lithium hexamethyldisilazide-ether 1:1 complex / 1) THF, -60 deg C, 30 min; 2) -60 deg C, 30 min, without cooling, 1 h
With potassium permanganate; N-benzyl-trimethylammonium hydroxide; magnesium sulfate; lithium hexamethyldisilazane; In ethanol; water;
DOI:10.1016/S0040-4020(01)92143-X
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