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Jungianol

Base Information Edit
  • Chemical Name:Jungianol
  • CAS No.:62885-78-3
  • Molecular Formula:C15H20O
  • Molecular Weight:216.32
  • Hs Code.:
  • Mol file:62885-78-3.mol
Jungianol

Synonyms:(1S,3S)-1,5-Dimethyl-3-(2-methyl-propenyl)-indan-4-ol;Jungianol;

Suppliers and Price of Jungianol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Jungianol Edit
Chemical Property:
  • PSA:20.23000 
  • LogP:4.25760 
Purity/Quality:
Safty Information:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

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Technology Process of Jungianol

There total 6 articles about Jungianol 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 sodium hydride; ethanethiol; In N,N-dimethyl-formamide; at 130 ℃; for 5h; Inert atmosphere;
DOI:10.1021/acs.joc.5b01071
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium hydroxide / ethanol / 20 °C
2.1: iodine; magnesium / diethyl ether
2.2: 2 h / 20 °C
3.1: triethylamine; methanesulfonyl chloride / tetrahydrofuran / 6 h / 0 - 20 °C
4.1: lithium; ammonia / tetrahydrofuran / 0.17 h / -78 °C
5.1: sodium hydride; ethanethiol / N,N-dimethyl-formamide / 5 h / 130 °C / Inert atmosphere
With ammonia; iodine; lithium; sodium hydride; magnesium; methanesulfonyl chloride; triethylamine; ethanethiol; sodium hydroxide; In tetrahydrofuran; diethyl ether; ethanol; N,N-dimethyl-formamide; 1.1: |Aldol Condensation;
DOI:10.1021/acs.joc.5b01071
Guidance literature:
Multi-step reaction with 3 steps
1: triethylamine; methanesulfonyl chloride / tetrahydrofuran / 6 h / 0 - 20 °C
2: lithium; ammonia / tetrahydrofuran / 0.17 h / -78 °C
3: sodium hydride; ethanethiol / N,N-dimethyl-formamide / 5 h / 130 °C / Inert atmosphere
With ammonia; lithium; sodium hydride; methanesulfonyl chloride; triethylamine; ethanethiol; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/acs.joc.5b01071
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