86504-35-0

Basic information

• Product Name: 3-(4-methylcyclohexan-3-onyl)butanal
• Synonyms: 3-(4-methylcyclohexan-3-onyl)butanal
• CAS NO: 86504-35-0
• Molecular Weight: 182.263
• Mol File: 86504-35-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3-(4-methylcyclohexan-3-onyl)butanal(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methylcyclohexan-3-onyl)butanal(86504-35-0)
• EPA Substance Registry System: 3-(4-methylcyclohexan-3-onyl)butanal(86504-35-0)

Safety Data

• Hazardous Substances Data: 86504-35-0(Hazardous Substances Data)

Upstream product

• 131569-57-8 (E)-3-[(1R,4R)-4-Methyl-3-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-but-2-enoic acid methyl ester 
• 131569-58-9 3-[(1R,4R)-4-Methyl-3-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-butyric acid methyl ester 
• 38049-24-0 1-[(1R,4R)-4-Methyl-3-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-ethanone 
• 38049-25-1 2-((2R,5R)-5-Isopropenyl-2-methyl-cyclohexyloxy)-tetrahydro-pyran 
• 131569-59-0 3-[(1R,4R)-4-Methyl-3-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-butan-1-ol 
• 6485-40-1 (R)-Carvone 
• 5524-05-0 (2R,5R)-5-isopropenyl-2-methylcyclohexanone 
• 201230-82-2 carbon monoxide 
• 3792-53-8 2-methyl-5-(prop-1-en-2-yl)cyclohexanone 
• 5524-05-0 (+)-dihydrocarvone 

Relevant articles and documents

Rh-catalyzed selective synthesis of 1,5-dimethylhexahydro-1H-inden-4(2H)-one via hydroformylation of (R)-carvone

This work reports domino hydroformylation, hydrogenation and intramolecular keto-aldol condensation reactions for the selective synthesis of 1,5-dimethylhexahydro-1H-inden-4(2H)-one obtained from (R)-carvone and dihydrocarvone under homogeneous hydroformy

Studies on the Liverwort Sesquiterpene Alcohol Tamariscol. Synthesis and Absolute Configuration

The relative configuration of the liverwort sesquiterpene alcohol (-)-tamariscol 1 has been confirmed by total synthesis and the absolute configuration has been established from the CD spectrum of the hydrindanone degradation product from (-)-1.

Hydroformylation of chiral terpenes with PtCl(SnCl3)-(bis-phosphine) as catalyst

(+)-R-Limonene and (-)-R-carvone undergo hydroformylation in the presence of catalytic Pt-bisphosphine-SnCl2 systems to yield exclusively the linear products.The internal double bond and the carbonyl group remain intact in both substrates during the react