40916-61-8 Usage
Uses
Used in Pharmaceutical Research:
1-Propanol, 2-(MethylaMino)-, hydrochloride, (S)(9CI) is utilized in pharmaceutical research for the development of medications targeting the central nervous system. Its psychoactive properties make it a subject of interest for understanding the mechanisms of stimulant action and addiction.
Used in Forensic Toxicology:
In forensic toxicology, 1-Propanol, 2-(MethylaMino)-, hydrochloride, (S)- (9CI) is identified and analyzed to determine the presence of illicit substances in biological samples. Its detection is crucial in cases involving substance abuse or poisoning.
Used in Drug Education and Awareness Programs:
1-Propanol, 2-(MethylaMino)-, hydrochloride, (S)(9CI) is featured in drug education and awareness programs to inform the public about the dangers of substance abuse, particularly the risks associated with methamphetamine use.
Used in Regulatory and Law Enforcement Agencies:
This chemical is monitored by regulatory and law enforcement agencies to control its distribution and prevent illegal trafficking, given its high potential for abuse and the severe health and social consequences associated with its misuse.
Check Digit Verification of cas no
The CAS Registry Mumber 40916-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,1 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40916-61:
(7*4)+(6*0)+(5*9)+(4*1)+(3*6)+(2*6)+(1*1)=108
108 % 10 = 8
So 40916-61-8 is a valid CAS Registry Number.
40916-61-8Relevant academic research and scientific papers
N-Methylation and Trideuteromethylation of Amines via Magnesium-Catalyzed Reduction of Cyclic and Linear Carbamates
Magre, Marc,Szewczyk, Marcin,Rueping, Magnus
supporting information, p. 3209 - 3214 (2020/04/10)
A new reduction of carbamates to N-methyl amines is presented. The magnesium-catalyzed reduction reaction allows the conversion of cyclic and linear carbamates, including N-Boc protected amines, into the corresponding N-methyl amines and amino alcohols which are of significant interest due to their presence in many biologically active molecules. Furthermore, the reduction can be extended to the formation of N-trideuteromethyl labeled amines.
