124549-80-0

Basic information

• Product Name: 2β-Hydroxy-4,6,6-trimethylcyclohex-3-ene-1β-carboxylate
• CAS NO: 124549-80-0
• Molecular Weight: 184.235
• Mol File: 124549-80-0.mol

Chemical Properties

• CAS DataBase Reference: 2β-Hydroxy-4,6,6-trimethylcyclohex-3-ene-1β-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 2β-Hydroxy-4,6,6-trimethylcyclohex-3-ene-1β-carboxylate(124549-80-0)
• EPA Substance Registry System: 2β-Hydroxy-4,6,6-trimethylcyclohex-3-ene-1β-carboxylate(124549-80-0)

Safety Data

• Hazardous Substances Data: 124549-80-0(Hazardous Substances Data)

Upstream product

• 78-59-1 3,5,5-Trimethylcyclohex-2-en-1-one 
• 124-38-9 carbon dioxide 

Downstream Products

• 96624-37-2 6a-epi-Yuehchukene 
• 124549-83-3 (1S,4S)-4-(1H-Indol-3-yl)-4,6,6-trimethyl-cyclohex-2-enecarboxylic acid 
• 124549-83-3 (1R,4S)-4-(1H-Indol-3-yl)-4,6,6-trimethyl-cyclohex-2-enecarboxylic acid 
• 135630-41-0 10bα-(3-Indolyl)-5-(p-toluenesulfonyl)-7,7,9-trimethyl-5,6aα,7,8,10aβ,10bα-hexahydroindeno-<2,1-b>indole 
• 124568-68-9 5-Benzoyl-6β-(3-indolyl)-7,7,9-trimethyl-5,6β,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole 
• 124568-69-0 Indoline 
• 135630-40-9 6α-Acetoxy-5-(p-toluenesulfonyl)-7,7,9-trimethyl-5,6α,6aα,7,8,10aβ-hexahydroindeno-<2,1-b>indole 
• 124549-88-8 ((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 
• 135630-37-4 5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole 
• 135630-39-6 6α-Hydroxy-5-(p-toluenesulfonyl)-7,7,9-trimethyl-5,6α,6aα,7,8,10aβ-hexahydroindeno-<2,1-b>indole 
• 135630-38-5 6-Oxo-5-(p-toluenesulfonyl)-7,7,9-trimethyl-5,6,6aα,7,8,10aβ-hexahydroindeno-<2,1-b>indole 
• 124549-82-2 2α-(3-Indolyl)-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic acid 
• 124549-85-5 (1S,2R)-2-(1H-Indol-3-yl)-4,6,6-trimethyl-cyclohex-3-enecarbonyl chloride 
• 96624-37-2 (+/-)-yuehchukene 

Relevant articles and documents

A general approach to the total synthesis of yuehchukene and its analogues. A novel anti-implantation agent

A versatile synthetic strategy has been developed for the synthesis of the interesting dimeric indole natural product yuehchukene (17) and its epimer, 6a-epi-yuehchukene (22). Due to the anti-implantation activity associated with 17, it is important to develop a synthetic route not only to 17, but to a family of yuehchukene analogues with better chemical stability and/or elevated biological activity. The strategy described here and which utilizes the readily available and inexpensive isophorone (1) satisfies these requirements.