41683-99-2 Usage
Classification
Psychoactive drug
Belongs to the amphetamine class of compounds
Chemical structure
Derivative of amphetamine
Features a chlorinated phenethylamine structure
Mechanism of action
Serotonin-norepinephrine-dopamine releasing agent
Acts as a releasing agent for these neurotransmitters
Effects
Stimulant and entactogenic
Produces feelings of increased energy, euphoria, and empathy
Adverse effects
Potential risks
Increased heart rate
Elevated blood pressure
Neurotoxicity when taken in high doses
Legal status
Controlled substance
Considered a controlled substance in many countries due to its psychoactive properties and potential for harm
Check Digit Verification of cas no
The CAS Registry Mumber 41683-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,8 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41683-99:
(7*4)+(6*1)+(5*6)+(4*8)+(3*3)+(2*9)+(1*9)=132
132 % 10 = 2
So 41683-99-2 is a valid CAS Registry Number.
41683-99-2Relevant academic research and scientific papers
Ind2TiMe2-catalyzed addition of methyl- and ethylamine to alkynes
Marcsekova, Klaudia,Wegener, Bernd,Doye, Sven
, p. 4843 - 4851 (2007/10/03)
We describe a very simple hydrogenation-like experimental protocol for the addition of gaseous methyl- and ethylamine to alkynes in the presence of Ind2TiMe2 as the catalyst. For efficient hydroamination reactions it is sufficient to stir a mixture of the alkyne and the catalyst in toluene at temperatures between 80°C (terminal alkynes) and 105°C (internal alkynes) under a constant pressure of 1 atm of the corresponding amine. After subsequent reduction of the initially formed imines, methyl- and ethylamine derivatives are the final products of the described one-pot reaction sequences. In the case of 2-alkyl-1-phenylalkynes as starting materials, biologically interesting 2-phenylethylamine derivatives possessing a small methyl or ethyl substituent at the N atom are easily accessible by the new reaction protocol. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.
