100692-55-5

Basic information

• Product Name: 1-Cyclohexene-1-methanol, 4-(1-methylethyl)-, (S)-
• CAS NO: 100692-55-5
• Molecular Formula: C10H18O
• Molecular Weight: 154.252
• Mol File: 100692-55-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Cyclohexene-1-methanol, 4-(1-methylethyl)-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Cyclohexene-1-methanol, 4-(1-methylethyl)-, (S)-(100692-55-5)
• EPA Substance Registry System: 1-Cyclohexene-1-methanol, 4-(1-methylethyl)-, (S)-(100692-55-5)

Safety Data

• Hazardous Substances Data: 100692-55-5(Hazardous Substances Data)

Upstream product

• 57717-97-2 (R)-Perillyl alcohol 
• 67-56-1 methanol 
• 56246-58-3 β-pinene oxide 
• 23963-70-4 (S)-4-Isopropyl-cyclohex-1-enecarbaldehyde 
• 555-31-7 aluminum isopropoxide 
• 536-59-4 (-)-perillyl alcohol 

Downstream Products

• 19876-47-2 (-)-O-(3.5-dinitro-benzoyl)-phellandrol 
• 211797-34-1 (2R,5S)-5-isopropyl-2-{[(triisopropylsilyl)oxy]methyl}cyclohexanone 
• 211797-32-9 (4S)-4-isopropyl-2-(pent-4-enyl)cyclohex-1-en-1-ylmethyl acetate 
• 211797-36-3 (4S)-4-isopropyl-2-(pent-4-enyl)cyclohex-1-en-1-carboxaldehyde 
• 211797-35-2 (1R,2R,5S)-2-(hydroxymethyl)-5-isopropyl-1-(pent-4-enyl)cyclohexanol 
• 441332-60-1 ((S)-4-Isopropyl-2-pent-4-enyl-cyclohex-1-enyl)-methanol 
• 1026837-87-5 (5S)-5-isopropyl-2-methylene-1-(4-pentenyl)-1-phenylsulfonylcyclohexane 
• 936031-86-6 C₁₇H₂₅NO₃S 
• 1027081-47-5 ((S)-5-Isopropyl-2-methylene-cyclohexanesulfinyl)-benzene 
• 211797-33-0 triisopropyl {[(4S)-4-isopropylcyclohex-1-enyl]methoxy}silane 

Relevant articles and documents

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Synthesis and AChE inhibitory activity of new chiral tetrahydroacridine analogues from terpenic cyclanones

This work describes the enantioselective synthesis of a new series of terpenic chiral 9-aminotetrahydroacridine analogues. Several chiral ketones were synthesized from natural monoterpenes in an optically active form and subjected to the cyclodehydration reactions with anthranilonitrile in the presence of BF3·Et2O as catalyst. The 9-aminotetrahydroacridine analogues were tested as acetylcholinesterase (AChE) inhibitors. Based on qualitative structure-activity relationship some trends are suggested.

Allyl sulfones as precursors to allylzincs in the palladium-catalyzed zinc-ene cyclization: Highly efficient synthesis of enantiopure (-)-erythrodiene

(Chemical Equation Presented) Easily prepared allyl phenyl sulfones, capable of introduction of the alkene by electrophilic α-substitution, are superior to allyl acetates as substrates for Pd-catalyzed Zn-ene cyclizations, providing C5 or C4N r