1214747-73-5

Basic information

• Product Name: (2R,5S)-2,5-diisopropylcyclohexanone
• Synonyms: (2R,5S)-2,5-diisopropylcyclohexanone
• CAS NO: 1214747-73-5
• Molecular Weight: 182.306
• Mol File: 1214747-73-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,5S)-2,5-diisopropylcyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,5S)-2,5-diisopropylcyclohexanone(1214747-73-5)
• EPA Substance Registry System: (2R,5S)-2,5-diisopropylcyclohexanone(1214747-73-5)

Safety Data

• Hazardous Substances Data: 1214747-73-5(Hazardous Substances Data)

Upstream product

• 4789-29-1 trans-1,4-diisopropylcyclohexane 
• 114300-89-9 1,4-diisopropyl-1,4-cyclohexadiene 
• 1214747-79-1 (2R,5S)-2-isopropyl-5-(propen-2-yl)-cyclohexanone 

Relevant articles and documents

SYNTHESIS AND APPLICATION OF CHIRAL SUBSTITUTED POLYVINYLPYRROLIDINONES

Chiral polyvinylpyrrolidinone (CSPVP), complexes of CSPVP with a core species, such as a metallic nanocluster catalyst, and enantioselective oxidation reactions utilizing such complexes are disclosed. The CSPVP complexes can be used in asymmetric oxidation of diols, enantioselective oxidation of alkenes, and carbon-carbon bond forming reactions, for example. The CSPVP can also be complexed with biomolecules such as proteins, DNA, and RNA, and used as nanocarriers for siRNA or dsRNA delivery.

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.