88069-93-6

Basic information

• Product Name: 1-Propanone, 1-(4-phenylcyclohexyl)-, trans-
• CAS NO: 88069-93-6
• Molecular Formula: C15H20O
• Molecular Weight: 216.323
• Mol File: 88069-93-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 1-(4-phenylcyclohexyl)-, trans-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 1-(4-phenylcyclohexyl)-, trans-(88069-93-6)
• EPA Substance Registry System: 1-Propanone, 1-(4-phenylcyclohexyl)-, trans-(88069-93-6)

Safety Data

• Hazardous Substances Data: 88069-93-6(Hazardous Substances Data)

Usage

Chemical structure

Contains a three-carbon ketone chain with a double bond between the first and second carbons, and a phenyl group attached to a cyclohexane ring.

Physical properties

Ketamine is a white or off-white crystalline powder that is soluble in water and can be formulated into injectable or intranasal solutions.

Medical uses

Ketamine is used as a sedative and anesthetic in both human and veterinary medicine. It is also being studied as a potential treatment for depression, PTSD, and other mental health disorders.

Mechanism of action

Ketamine works by blocking the transmission of pain signals in the brain and nervous system, and also has psychedelic effects that can induce altered states of consciousness, hallucinations, and out-of-body experiences.

Legal status

Ketamine is a controlled substance due to its potential for abuse and addiction. It is classified as a Schedule III drug in the United States, meaning it has a moderate to low potential for physical dependence and a high potential for psychological dependence.

Upstream product

• 1655-03-4 1-cyclohex-1-enyl-propan-1-one 
• 71-43-2 benzene 
• 88069-91-4 1-propionyl-2-chlorocyclohexane 

Downstream Products

• 81005-00-7 trans-4-(4-Propylcyclohexyl)benzoesaeurechlorid 
• 81930-17-8 4-(4-Propyl-cyclohexyl)-benzoic acid 4-cyano-phenyl ester 
• 65355-29-5 4-(trans-4'-propylcyclohexyl)-benzoic acid 
• 73163-49-2 4-(trans-4-propylcyclohexyl)benzamide 
• 78531-61-0 1-[4-(4-Propyl-cyclohexyl)-phenyl]-ethanone 
• 61203-99-4 trans-4-propyl-(4'-cyanophenyl)cyclohexane 
• 61203-94-9 trans-4-propyl-1-phenylcyclohexane 
• 1466-73-5 trans-4-phenylcyclohexanecarboxylic acid 

Relevant articles and documents

SYNTHESIS OF TRANS-4-ALKYL-1-PHENYLCYCLOHEXANES AND THEIR DERIVATIVES

The alkylation of benzene by 1-alkanoyl-2-chlorocyclohexanes and 1-alkanoyl-1-cyclohexenes leads to the formation of cis- and trans-4-alkanoyl-1-phenylcyclohexanes, the yields of which increase with increase in the reaction temperature. trans-4-Alkyl-1-phenylcyclohexanes were obtained from 4-alkanoyl-1-phenylcyclohexanes and also from the products from the reaction of 4-alkylcyclohexanones with phenylmagnesium bromide.Some mesomorphous derivatives of these hydrocarbons were synthesized.