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(1R,3aR,4S,7aR)-4-benzenesulfonyl-7a-methyl-1-<(1R,4S)-1,4,5-trimethyl-hexyl>-octahydroindene

Base Information Edit
  • Chemical Name:(1R,3aR,4S,7aR)-4-benzenesulfonyl-7a-methyl-1-<(1R,4S)-1,4,5-trimethyl-hexyl>-octahydroindene
  • CAS No.:71830-70-1
  • Molecular Formula:C25H40O2S
  • Molecular Weight:404.657
  • Hs Code.:
  • Mol file:71830-70-1.mol
(1R,3aR,4S,7aR)-4-benzenesulfonyl-7a-methyl-1-<(1R,4S)-1,4,5-trimethyl-hexyl>-octahydroindene

Synonyms:(1R,3aR,4S,7aR)-4-benzenesulfonyl-7a-methyl-1-<(1R,4S)-1,4,5-trimethyl-hexyl>-octahydroindene

Suppliers and Price of (1R,3aR,4S,7aR)-4-benzenesulfonyl-7a-methyl-1-<(1R,4S)-1,4,5-trimethyl-hexyl>-octahydroindene
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (1R,3aR,4S,7aR)-4-benzenesulfonyl-7a-methyl-1-<(1R,4S)-1,4,5-trimethyl-hexyl>-octahydroindene Edit
Chemical Property:
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MSDS Files:

SDS file from LookChem

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Technology Process of (1R,3aR,4S,7aR)-4-benzenesulfonyl-7a-methyl-1-<(1R,4S)-1,4,5-trimethyl-hexyl>-octahydroindene

There total 11 articles about (1R,3aR,4S,7aR)-4-benzenesulfonyl-7a-methyl-1-<(1R,4S)-1,4,5-trimethyl-hexyl>-octahydroindene 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: KMnO4
3: 1.) Pb(OAc)4, pyridine, 2.) NaBH4, CeCl3*7H2O / 1.) CH2Cl2, 0 deg C, 10 min, 2.) CH3OH, 0 deg C, 3 h
4: 1.80 g / H2 / Pd/C / methanol / 16 h
5: Jones reagent / acetone
6: BF3*2H2O / CH2Cl2 / 16 h / 0 °C
7: 1.51 g / m-CPBA / CH2Cl2 / 3 h / 0 °C
8: 66 percent / LiAlH4 / tetrahydrofuran / 0.33 h / Heating
With pyridine; lead(IV) acetate; sodium tetrahydroborate; potassium permanganate; lithium aluminium tetrahydride; jones reagent; cerium(III) chloride; boron trifluoride; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; acetone;
Guidance literature:
Multi-step reaction with 5 steps
1: 1.80 g / H2 / Pd/C / methanol / 16 h
2: Jones reagent / acetone
3: BF3*2H2O / CH2Cl2 / 16 h / 0 °C
4: 1.51 g / m-CPBA / CH2Cl2 / 3 h / 0 °C
5: 66 percent / LiAlH4 / tetrahydrofuran / 0.33 h / Heating
With lithium aluminium tetrahydride; jones reagent; boron trifluoride; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; acetone;
Guidance literature:
Multi-step reaction with 7 steps
2: 1.) Pb(OAc)4, pyridine, 2.) NaBH4, CeCl3*7H2O / 1.) CH2Cl2, 0 deg C, 10 min, 2.) CH3OH, 0 deg C, 3 h
3: 1.80 g / H2 / Pd/C / methanol / 16 h
4: Jones reagent / acetone
5: BF3*2H2O / CH2Cl2 / 16 h / 0 °C
6: 1.51 g / m-CPBA / CH2Cl2 / 3 h / 0 °C
7: 66 percent / LiAlH4 / tetrahydrofuran / 0.33 h / Heating
With pyridine; lead(IV) acetate; sodium tetrahydroborate; lithium aluminium tetrahydride; jones reagent; cerium(III) chloride; boron trifluoride; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; acetone;
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