7,7,9-Trimethyl-5,6,6a,7,8,10a-hexahydroindeno[2,1-b]indol-6-ol

Base Information

• Chemical Name: 7,7,9-Trimethyl-5,6,6a,7,8,10a-hexahydroindeno[2,1-b]indol-6-ol
• CAS No.: 143615-53-6
• Molecular Formula: C₁₈H₂₁NO
• Molecular Weight: 267.371
• DSSTox Substance ID: DTXSID90555594
• Mol file: 143615-53-6.mol

Synonyms:143615-53-6;7,7,9-Trimethyl-5,6,6a,7,8,10a-hexahydroindeno[2,1-b]indol-6-ol;DTXSID90555594

Chemical Property of 7,7,9-Trimethyl-5,6,6a,7,8,10a-hexahydroindeno[2,1-b]indol-6-ol

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 267.162314293
• Heavy Atom Count: 20
• Complexity: 441

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC2C(C(C3=C2C4=CC=CC=C4N3)O)C(C1)(C)C

Technology Process of 7,7,9-Trimethyl-5,6,6a,7,8,10a-hexahydroindeno[2,1-b]indol-6-ol

There total 1 articles about 7,7,9-Trimethyl-5,6,6a,7,8,10a-hexahydroindeno[2,1-b]indol-6-ol 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:

Reference yield: 16.0%

(1S,2R)-2-(1-Benzoyl-1H-indol-3-yl)-4,6,6-trimethyl-cyclohex-3-enecarbaldehyde → 6α-Hydroxy-7,7,9-trimethyl-5,6α,6aα,7,8,10aβ-hexahydroindeno-<2,1-b>indole (120094-32-8,124600-45-9,135683-71-5,143615-53-6) + (1S,2R)-2-(1H-Indol-3-yl)-4,6,6-trimethyl-cyclohex-3-enecarbaldehyde

Guidance literature:

With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃;

DOI:10.1039/c39930000510

Reference yield: 97.0%

indole (120-72-9) + 6α-Hydroxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole (120094-32-8,124600-45-9,135683-71-5,143615-53-6) → (+/-)-yuehchukene (96624-37-2,124600-46-0,139241-53-5,139241-58-0)

Guidance literature:

With lithium perchlorate; In diethyl ether; for 0.5h; Ambient temperature;

DOI:10.1039/c39930000510

Reference yield: 86.0%

indole (120-72-9) + 6β-Hydroxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole (120094-32-8,124600-45-9,135683-71-5,143615-53-6) → (+/-)-yuehchukene (96624-37-2,124600-46-0,139241-53-5,139241-58-0)

Guidance literature:

With lithium perchlorate; In diethyl ether; for 3h; Ambient temperature;

DOI:10.1039/c39930000510

Downstream raw materials:

(+/-)-yuehchukene

5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

((6R,6aR,10aR)-6-Indol-1-yl-7,7,9-trimethyl-6a,7,8,10a-tetrahydro-6H-indeno[2,1-b]indol-5-yl)-phenyl-methanone

Indoline

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