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(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R,3E,5S)-5-methylhept-3-en-2-yl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol (non-preferred name)

Base Information
  • Chemical Name:(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R,3E,5S)-5-methylhept-3-en-2-yl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol (non-preferred name)
  • CAS No.:54278-89-6
  • Molecular Formula:C27H44O
  • Molecular Weight:384.6377
  • Hs Code.:
(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R,3E,5S)-5-methylhept-3-en-2-yl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol (non-preferred name)

Synonyms:

Suppliers and Price of (3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R,3E,5S)-5-methylhept-3-en-2-yl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol (non-preferred name)
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of (3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R,3E,5S)-5-methylhept-3-en-2-yl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol (non-preferred name)
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:479.884°C at 760 mmHg 
  • Flash Point:208.3°C 
  • Density:1g/cm3 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of (3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R,3E,5S)-5-methylhept-3-en-2-yl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol (non-preferred name)

There total 18 articles about (3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R,3E,5S)-5-methylhept-3-en-2-yl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol (non-preferred name) 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 7 steps
2: 885 mg / sodium bis(2-methoxyethoxy)aluminum hydride (Red-Al, 70percent in toluene) / diethyl ether / 48 h / Heating
3: 774 mg / propionic acid / xylene / 2 h / 130 °C
4: 503 mg / lithium aluminum hydride / diethyl ether / 1 h / Heating
5: 521 mg / pyridine / Ambient temperature; overnight
6: 290 mg / lithium aluminum hydride / tetrahydrofuran / 1 h / Heating
7: 216 mg / p-toluenesulfonic acid / dioxane; H2O / 1 h / Heating
With lithium aluminium tetrahydride; toluene-4-sulfonic acid; propionic acid; sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran; 1,4-dioxane; pyridine; diethyl ether; water; xylene;
DOI:10.1021/jo00133a036
Guidance literature:
Multi-step reaction with 6 steps
1: 0.969 g / H2, quinoline / Lindlar catalyst / hexane / 3 h / Ambient temperature
2: 481 mg / propionic acid / xylene / 2 h / 130 °C
3: 503 mg / lithium aluminum hydride / diethyl ether / 1 h / Heating
4: 521 mg / pyridine / Ambient temperature; overnight
5: 290 mg / lithium aluminum hydride / tetrahydrofuran / 1 h / Heating
6: 216 mg / p-toluenesulfonic acid / dioxane; H2O / 1 h / Heating
With quinoline; lithium aluminium tetrahydride; hydrogen; toluene-4-sulfonic acid; propionic acid; Lindlar's catalyst; In tetrahydrofuran; 1,4-dioxane; pyridine; diethyl ether; hexane; water; xylene;
DOI:10.1021/jo00133a036
Guidance literature:
Multi-step reaction with 7 steps
2: 90 percent / quinoline / Lindlar catalyst
3: 65 percent / propionic acid / toluene / Heating
4: LiAlH4
5: triethylamine
6: LiAlH4
7: H(1+)
With quinoline; lithium aluminium tetrahydride; hydrogen cation; propionic acid; triethylamine; Lindlar's catalyst; In toluene;
DOI:10.1016/S0040-4039(01)90046-2
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