23923-61-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-phenylcyclohexyl)ethanone is used as a research chemical for the development of new anesthetics and for studying the effects of dissociative drugs on the human brain. Its unique properties allow scientists to gain insights into the mechanisms of anesthesia and the potential for developing safer alternatives.
Used in Forensic Science:
1-(2-phenylcyclohexyl)ethanone is used as a reference compound in forensic science for the identification and analysis of substances related to drug abuse and criminal investigations. Its distinct chemical properties make it a valuable tool in the detection and confirmation of PCP use in cases involving substance abuse.
Used in Drug Enforcement:
1-(2-phenylcyclohexyl)ethanone is used by drug enforcement agencies as a reference substance to help identify and classify controlled substances. Its classification as a Schedule II controlled substance in the United States highlights its potential for abuse and dependence, making it a critical component in the efforts to regulate and control the distribution and use of dissociative drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 23923-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,2 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23923-61:
(7*2)+(6*3)+(5*9)+(4*2)+(3*3)+(2*6)+(1*1)=107
107 % 10 = 7
So 23923-61-7 is a valid CAS Registry Number.
23923-61-7Relevant academic research and scientific papers
Palladium-catalyzed site-selective arylation of aliphatic ketones enabled by a transient ligand
Pan, Lei,Yang, Ke,Li, Guigen,Ge, Haibo
supporting information, p. 2759 - 2762 (2018/03/21)
Transition metal-catalyzed direct C-H bond functionalization enabled by transient ligands has become an attractive topic. Here we report a palladium-catalyzed site-selective arylation of β-C(sp3)-H bonds in aliphatic ketones with β-alanine as the transient ligand.
Rhodium-Catalyzed Intramolecular Cyclopropanation of α-Diazo β-Keto Nitriles Containing an Unsaturated Substituted Cycloalkyl Group
Zhu, Jia-Liang,Wu, Yung-Peng
supporting information, p. 1467 - 1472 (2017/07/22)
Several α-diazo β-keto nitriles bearing trans -2-allyl-, -vinyl-, or -phenylcycloalkyl groups were prepared and their intramolecular cyclopropanation reactions were examined. In the presence of Rh 2 (OAc) 4 (1 mol%) as a catalyst, th
Palladium(II)-catalyzed Michael-type addition reactions using aryltin compounds
Ohe,Wakita,Motofusa,Cho,Ohe,Uemura
, p. 2149 - 2155 (2007/10/03)
A variety of aryltin compounds can be employed for Michael-type hydroarylation reactions to α,β-unsaturated ketones and aldehydes in the presence of a catalytic amount of palladium(II) salt in acetic acid under air. Each reaction is much accelerated in the presence of a soluble metal chloride such as LiCl, MgCl2, and CaCl2. It is found that slightly fewer than four aryl groups of tetraaryltins can be transferred to the products in this arylation.
