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(1S,3aS,4S,7aS)-(+)-1-acetoxy-7a-ethyl-3a,4,5,6,7,7a-hexahydro-4-phenylsulfonylmethyl-indan-5-one

Base Information
  • Chemical Name:(1S,3aS,4S,7aS)-(+)-1-acetoxy-7a-ethyl-3a,4,5,6,7,7a-hexahydro-4-phenylsulfonylmethyl-indan-5-one
  • CAS No.:101750-96-3
  • Molecular Formula:C20H26O5S
  • Molecular Weight:378.489
  • Hs Code.:
(1S,3aS,4S,7aS)-(+)-1-acetoxy-7a-ethyl-3a,4,5,6,7,7a-hexahydro-4-phenylsulfonylmethyl-indan-5-one

Synonyms:(1S,3aS,4S,7aS)-(+)-1-acetoxy-7a-ethyl-3a,4,5,6,7,7a-hexahydro-4-phenylsulfonylmethyl-indan-5-one

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Chemical Property of (1S,3aS,4S,7aS)-(+)-1-acetoxy-7a-ethyl-3a,4,5,6,7,7a-hexahydro-4-phenylsulfonylmethyl-indan-5-one
Chemical Property:
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Technology Process of (1S,3aS,4S,7aS)-(+)-1-acetoxy-7a-ethyl-3a,4,5,6,7,7a-hexahydro-4-phenylsulfonylmethyl-indan-5-one

There total 10 articles about (1S,3aS,4S,7aS)-(+)-1-acetoxy-7a-ethyl-3a,4,5,6,7,7a-hexahydro-4-phenylsulfonylmethyl-indan-5-one 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 hydrogenchloride; hydrogen; palladium on activated charcoal; In ethanol; under 760 Torr; Ambient temperature;
DOI:10.1016/S0040-4020(01)82341-3
Guidance literature:
Multi-step reaction with 9 steps
1: 1.) n-butyllithium / 1.) tetrahydrofuran/hexane, -78 deg C, then to -35 deg C, 1.5 h, 2.) -70 deg C, then 10 deg C, 2 d
2: 65 percent / mercury(II) chloride, calcium carbonate / acetonitrile; H2O / 9 h / Heating
3: 85 percent / pyridine / CH2Cl2 / 2 h / 20 °C
4: 75 percent / triethylamine, hydroquinone / tetrahydrofuran / 14 h / Heating
5: 53 percent / saccharomyces cerevisiae (2.346), glucose, corn starch, K2HPO4, NaNO3, KH2PO4, MgSO4, KCl, FeSO4, 6 N aq. sodium hydroxide, toween 80 / ethanol / 25 h / 30 °C / pH= 6.7-7.0
6: 55 mg / pyridine / 1 h / 100 °C
7: 110 mg / m-chloroperbenzoic acid / CH2Cl2 / 2 h / 15 °C
8: 63 percent / p-toluenesulfonic acid monohydrate / benzene / 40 h / 90 - 100 °C
9: 70 percent / H2, 1 N HCl / 10 percent Pd-C / ethanol / 760 Torr / Ambient temperature
With pyridine; hydrogenchloride; sodium hydroxide; sodium nitrate; dipotassium hydrogenphosphate; potassium dihydrogenphosphate; n-butyllithium; D-glucose; saccharomyces cerevisiae (2.346); toween 80; potassium chloride; hydrogen; magnesium sulfate; toluene-4-sulfonic acid; iron(II) sulfate; triethylamine; hydroquinone; 3-chloro-benzenecarboperoxoic acid; calcium carbonate; mercury dichloride; corn starch; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile; benzene;
DOI:10.1016/S0040-4020(01)82341-3
Guidance literature:
Multi-step reaction with 7 steps
1: 85 percent / pyridine / CH2Cl2 / 2 h / 20 °C
2: 75 percent / triethylamine, hydroquinone / tetrahydrofuran / 14 h / Heating
3: 53 percent / saccharomyces cerevisiae (2.346), glucose, corn starch, K2HPO4, NaNO3, KH2PO4, MgSO4, KCl, FeSO4, 6 N aq. sodium hydroxide, toween 80 / ethanol / 25 h / 30 °C / pH= 6.7-7.0
4: 55 mg / pyridine / 1 h / 100 °C
5: 110 mg / m-chloroperbenzoic acid / CH2Cl2 / 2 h / 15 °C
6: 63 percent / p-toluenesulfonic acid monohydrate / benzene / 40 h / 90 - 100 °C
7: 70 percent / H2, 1 N HCl / 10 percent Pd-C / ethanol / 760 Torr / Ambient temperature
With pyridine; hydrogenchloride; sodium hydroxide; sodium nitrate; dipotassium hydrogenphosphate; potassium dihydrogenphosphate; D-glucose; saccharomyces cerevisiae (2.346); toween 80; potassium chloride; hydrogen; magnesium sulfate; toluene-4-sulfonic acid; iron(II) sulfate; triethylamine; hydroquinone; 3-chloro-benzenecarboperoxoic acid; corn starch; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; benzene;
DOI:10.1016/S0040-4020(01)82341-3
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