10509-87-2 Usage
Uses
Used in Pharmaceutical Research:
α,α'-Dimethyldiphenethylamine Hydrochloride is used as a research compound for studying its psychostimulatory effects and potential applications in the development of medications targeting the central nervous system. Its structural similarity to amphetamines allows researchers to explore its interactions with neurotransmitters and receptors, which could lead to the discovery of new therapeutic agents.
Used in Neuropharmacology:
In the field of neuropharmacology, α,α'-Dimethyldiphenethylamine Hydrochloride is utilized as a tool to investigate the mechanisms of action of psychostimulant drugs. Understanding its effects on neurotransmitter release and uptake can provide insights into the development of treatments for various neurological and psychiatric disorders.
Used in Drug Development:
α,α'-Dimethyldiphenethylamine Hydrochloride is used as a lead compound in the development of new psychoactive substances. Its potential psychostimulatory effects make it a candidate for further research and optimization to create safer and more effective medications for the treatment of attention deficit hyperactivity disorder (ADHD), narcolepsy, and other conditions that may benefit from stimulant therapy.
Check Digit Verification of cas no
The CAS Registry Mumber 10509-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,0 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10509-87:
(7*1)+(6*0)+(5*5)+(4*0)+(3*9)+(2*8)+(1*7)=82
82 % 10 = 2
So 10509-87-2 is a valid CAS Registry Number.
10509-87-2Relevant academic research and scientific papers
REDUCTION OF ARYLALKYLAZOMETHINES WITH SODIUM BOROHYDRIDE
Dumpis, M. A.,Kudryashova, N. I.,Veresova, M. A.
, p. 1332 - 1337 (2007/10/02)
The secondary amines R1R2C6H3CH2CH(CH3)NHCHR5CHR6(CH2)nC6H3R3R4 were synthesized by the reduction of the respective azomethines with sodium borohydride.The reaction was conducted in anhydrous methanol in the presence of hydrogen chloride with the azomethine and hydrogen chloride in a molar ratio of 1:1.The yield was 50-90percent.The erythro and threo isomers were isolated, and the data from the IR spectra of the isomers are given.
