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(2S,6S)-2,6-diphenyltetrahydro-2H-thiopyran

Base Information Edit
  • Chemical Name:(2S,6S)-2,6-diphenyltetrahydro-2H-thiopyran
  • CAS No.:1438891-78-1
  • Molecular Formula:C17H18S
  • Molecular Weight:254.396
  • Hs Code.:
  • Mol file:1438891-78-1.mol
(2S,6S)-2,6-diphenyltetrahydro-2H-thiopyran

Synonyms:(2S,6S)-2,6-diphenyltetrahydro-2H-thiopyran

Suppliers and Price of (2S,6S)-2,6-diphenyltetrahydro-2H-thiopyran
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (2S,6S)-2,6-diphenyltetrahydro-2H-thiopyran Edit
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Technology Process of (2S,6S)-2,6-diphenyltetrahydro-2H-thiopyran

There total 5 articles about (2S,6S)-2,6-diphenyltetrahydro-2H-thiopyran 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 sodiumsulfide nonahydrate; In dimethyl sulfoxide; at 25 ℃; for 36h;
DOI:10.1016/j.tetasy.2013.03.021
Guidance literature:
Multi-step reaction with 5 steps
1: phosphorus pentachloride / 24 h / Reflux
2: aluminum (III) chloride
3: borane-THF; (S)-diphenylprolinol; Trimethyl borate
4: triethylamine / dichloromethane
5: sodiumsulfide nonahydrate / dimethyl sulfoxide / 36 h / 25 °C
With aluminum (III) chloride; borane-THF; sodiumsulfide nonahydrate; Trimethyl borate; (S)-diphenylprolinol; phosphorus pentachloride; triethylamine; In dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.tetasy.2013.03.021
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine / dichloromethane
2: sodiumsulfide nonahydrate / dimethyl sulfoxide / 36 h / 25 °C
With sodiumsulfide nonahydrate; triethylamine; In dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.tetasy.2013.03.021
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