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[2S,5R,6R]-3,3-dimethyl-4,4,7-trioxo-6-[6-(4-methylphenylsulfonyl)-isoxazol-3-ylmethyl]-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid diphenylmethyl

Base Information
  • Chemical Name:[2S,5R,6R]-3,3-dimethyl-4,4,7-trioxo-6-[6-(4-methylphenylsulfonyl)-isoxazol-3-ylmethyl]-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid diphenylmethyl
  • CAS No.:305796-55-8
  • Molecular Formula:C32H30N2O8S2
  • Molecular Weight:634.731
  • Hs Code.:
[2S,5R,6R]-3,3-dimethyl-4,4,7-trioxo-6-[6-(4-methylphenylsulfonyl)-isoxazol-3-ylmethyl]-4λ<sup>6</sup>-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid diphenylmethyl

Synonyms:[2S,5R,6R]-3,3-dimethyl-4,4,7-trioxo-6-[6-(4-methylphenylsulfonyl)-isoxazol-3-ylmethyl]-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid diphenylmethyl

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Chemical Property of [2S,5R,6R]-3,3-dimethyl-4,4,7-trioxo-6-[6-(4-methylphenylsulfonyl)-isoxazol-3-ylmethyl]-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid diphenylmethyl
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Technology Process of [2S,5R,6R]-3,3-dimethyl-4,4,7-trioxo-6-[6-(4-methylphenylsulfonyl)-isoxazol-3-ylmethyl]-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid diphenylmethyl

There total 9 articles about [2S,5R,6R]-3,3-dimethyl-4,4,7-trioxo-6-[6-(4-methylphenylsulfonyl)-isoxazol-3-ylmethyl]-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid diphenylmethyl 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 8 steps
1: 95 percent / acetone / 2 h / 20 °C
2: 72 percent / AIBN / toluene / 6 h / Heating
3: 75 percent / tributyltin hydride; AIBN / toluene / 3 h / 20 °C
4: 85 percent / ozone; dimethyl sulfide / CH2Cl2 / 15 h / 20 °C
5: 90 percent / hydroxylamine hydrochloride; sodium acetate / ethanol; H2O / 5 h / 20 °C
6: 83 percent / N-chlorosuccinimide / dimethylformamide / 2 h / 20 °C
7: (Bu3Sn)2O / benzene
8: bis(tributyltin) oxide / benzene / 2 h / 20 °C
With N-chloro-succinimide; dimethylsulfide; 2,2'-azobis(isobutyronitrile); hydroxylamine hydrochloride; tri-n-butyl-tin hydride; sodium acetate; ozone; bis(tri-n-butyltin)oxide; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene; benzene; 1: Alkylation / 2: Substitution / 3: Substitution / 4: Oxidation / 5: oxime formation / 6: Chlorination / 7: Elimination / 8: Cycloaddition;
DOI:10.1021/ol006256r
Guidance literature:
Multi-step reaction with 7 steps
1: 72 percent / AIBN / toluene / 6 h / Heating
2: 75 percent / tributyltin hydride; AIBN / toluene / 3 h / 20 °C
3: 85 percent / ozone; dimethyl sulfide / CH2Cl2 / 15 h / 20 °C
4: 90 percent / hydroxylamine hydrochloride; sodium acetate / ethanol; H2O / 5 h / 20 °C
5: 83 percent / N-chlorosuccinimide / dimethylformamide / 2 h / 20 °C
6: (Bu3Sn)2O / benzene
7: bis(tributyltin) oxide / benzene / 2 h / 20 °C
With N-chloro-succinimide; dimethylsulfide; 2,2'-azobis(isobutyronitrile); hydroxylamine hydrochloride; tri-n-butyl-tin hydride; sodium acetate; ozone; bis(tri-n-butyltin)oxide; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; benzene; 1: Substitution / 2: Substitution / 3: Oxidation / 4: oxime formation / 5: Chlorination / 6: Elimination / 7: Cycloaddition;
DOI:10.1021/ol006256r
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