65712-49-4 Usage
Uses
Used in Pharmaceutical Research:
2,4-bis(2-methylphenyl)-3-azabicyclo[3.3.1]nonan-9-one is used as a research compound for studying the effects of dopamine reuptake inhibition on the central nervous system. Its psychoactive properties make it a valuable tool in understanding the mechanisms of action and potential therapeutic applications in the treatment of neurological and psychiatric disorders.
Used in Controlled Substances Regulation:
Due to its high potential for abuse and associated adverse effects, 2,4-bis(2-methylphenyl)-3-azabicyclo[3.3.1]nonan-9-one is used as a reference substance in the development and enforcement of controlled substance regulations. Its classification as a controlled substance helps to prevent illegal manufacture, possession, and distribution, protecting public health and safety.
Used in Toxicology and Addiction Studies:
2,4-bis(2-methylphenyl)-3-azabicyclo[3.3.1]nonan-9-one is used as a model compound in toxicology and addiction research to investigate the adverse effects of psychoactive substances on the human body. Its association with addiction, cardiovascular complications, and psychiatric disturbances provides valuable insights into the risks and consequences of substance abuse.
Used in Forensic Analysis:
In forensic science, 2,4-bis(2-methylphenyl)-3-azabicyclo[3.3.1]nonan-9-one is used as a target analyte in the detection and analysis of controlled substances. Its identification in biological samples or seized materials can provide crucial evidence in criminal investigations related to drug trafficking and substance abuse.
Check Digit Verification of cas no
The CAS Registry Mumber 65712-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,1 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65712-49:
(7*6)+(6*5)+(5*7)+(4*1)+(3*2)+(2*4)+(1*9)=134
134 % 10 = 4
So 65712-49-4 is a valid CAS Registry Number.
65712-49-4Relevant academic research and scientific papers
Spontaneous generation of chirality and chiroptical spectra of N-nitroso-2,4-diaryl-3-azabicyclo[3.3.1]nonanes
Olszewska, Teresa,Milewska, Maria J.,Gdaniec, Maria,Polonski, Tadeusz
experimental part, p. 278 - 283 (2012/06/15)
The crystal structures of several bicyclic N-nitrosamines indicate that they crystallize in the chiral (Sohncke) space group P212 121 as conglomerates. This allows the resolution of these compounds by manual picking of the
Synthesis, complete NMR spectral assignments, and antifungal screening of new 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-one oxime derivatives
Parthiban, Paramasivam,Rathika, Paramasivam,Park, Keun Soo,Jeong, Yeon Tae
experimental part, p. 79 - 93 (2010/07/10)
A series of differently substituted 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9- one oximes have been synthesized and their 1H and 13C NMR chemical shifts have been unambiguously assigned using H,H-COSY, NOESY, HSQC, and HMBC spectral data
2,4-Bis(o-tolyl)-3-azabicyclo[3.3.1]nonan-9-one
Vijayalakshmi,Parthasarathi,Venkatraj,Jeyaraman
, p. 1240 - 1241 (2007/10/03)
The crystal structure of 2,4-bis(o-tolyl)-3-azabicyclo[3.3.1]-nonan-9-one shows that the bicyclic ring system adopts the chair-chair conformation. The phenyl rings are equatorially disposed with respect to the bicyclic ring. A slight deviation is seen from the chair conformation in the case of cyclohexane ring. A mixture of cyclohexanone, o-tolualdehyde and ethanol was added to a warm solution of ammonium acetate in absolute ethanol. Crystals of the ketone were separated out and were washed.
