140848-06-2

Basic information

• Product Name: 2-Cyclohexene-1-methanol, 6-(4-methoxy-4-methylpentyl)-2,6-dimethyl-
• Synonyms: 2-Cyclohexene-1-methanol,6-(4-methoxy-4-methylpentyl)-2,6-dimethyl;1,3-dimethyl-2-(hydroxymethyl)-1-(4'-methoxy-4'-methylpentyl)cyclohex-3-ene;2,4-dimethyl-3-hydroxymethyl-4-(4-methoxy-4-methylpentyl)-cyclohex-1-ene
• CAS NO: 140848-06-2
• Molecular Formula: C16H30O2
• Molecular Weight: 254.413
• Mol File: 140848-06-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexene-1-methanol, 6-(4-methoxy-4-methylpentyl)-2,6-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexene-1-methanol, 6-(4-methoxy-4-methylpentyl)-2,6-dimethyl-(140848-06-2)
• EPA Substance Registry System: 2-Cyclohexene-1-methanol, 6-(4-methoxy-4-methylpentyl)-2,6-dimethyl-(140848-06-2)

Safety Data

• Hazardous Substances Data: 140848-06-2(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 106-28-5 Farnesol 

Relevant articles and documents

Cyclization and Rearrangements of Farnesol and Nerolidol Stereoisomers in Superacids

Acid-catalyzed cyclization of 2,3-trans- and 2,3-cis-farnesol proceeds regioselectively and stereospecifically, yielding drimenol and epi-drimenol, respectively.The trans and cis isomers of nerolidol undergo carbo- and heterocyclization reactions.The trans isomer gives tricyclic caged hydrocarbons with new skeletal types, while the rearrangements of the cis isomer produce derivatives of 2-oxabicyclodecane.The ICAR computer program was used to derive reasonable mechanisms for the acid-catalyzed transformations of nerolidol, and the probability of the mechanisms was evaluated by the molecular mechanics method.