65712-49-4 Usage
General Description
2,4-bis(2-methylphenyl)-3-azabicyclo[3.3.1]nonan-9-one, also known as WIN 48,098, is a chemical compound with psychoactive properties. It belongs to the cathinone class of drugs, which are known for their stimulant effects on the central nervous system. This specific compound has been found to act as a dopamine reuptake inhibitor, meaning it increases the levels of dopamine in the brain, leading to feelings of euphoria and increased energy. Due to its psychoactive effects, WIN 48,098 has been classified as a controlled substance in many countries and is illegal to manufacture, possess, or distribute without proper authorization. Its use has been associated with a range of adverse effects, including addiction, cardiovascular complications, and psychiatric disturbances.
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 articles and documents
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
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.
