100073-44-7 Usage
Uses
Used in Pharmaceutical Industry:
2-[(1-methylethyl)amino]-1-naphthalen-2-ylpropan-1-one hydrochloride is used as a key intermediate in the synthesis of various medications for its dopamine reuptake inhibitory properties.
Used in Treatment of ADHD:
2-[(1-methylethyl)amino]-1-naphthalen-2-ylpropan-1-one hydrochloride is used as a therapeutic agent for the treatment of attention deficit hyperactivity disorder (ADHD) due to its ability to inhibit dopamine reuptake, thereby increasing dopamine levels in the brain.
Used in Treatment of Narcolepsy:
2-[(1-methylethyl)amino]-1-naphthalen-2-ylpropan-1-one hydrochloride is used as a potential treatment for narcolepsy, a sleep disorder characterized by excessive daytime sleepiness and sudden loss of muscle tone, leveraging its dopamine reuptake inhibitory effects.
Used in Analgesic Applications:
2-[(1-methylethyl)amino]-1-naphthalen-2-ylpropan-1-one hydrochloride may be used as an analgesic agent due to its potential ability to inhibit the reuptake of norepinephrine and serotonin, contributing to pain relief.
Used in Regulatory Measures:
2-[(1-methylethyl)amino]-1-naphthalen-2-ylpropan-1-one hydrochloride is subject to careful regulation and control in its use and distribution due to its psychoactive properties and potential for misuse and abuse.
Check Digit Verification of cas no
The CAS Registry Mumber 100073-44-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,7 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100073-44:
(8*1)+(7*0)+(6*0)+(5*0)+(4*7)+(3*3)+(2*4)+(1*4)=57
57 % 10 = 7
So 100073-44-7 is a valid CAS Registry Number.
100073-44-7Relevant academic research and scientific papers
REDUCTION OF 1-(2-NAPHTHYL)-2-ALKYLAMINO-1-PROPANONES. I. HYDROGENATION OF THE NAPHTHALENE RING
Dumpis, M. A.,Kudryashova, N. I.,Khromov-Borisov, N. V.
, p. 893 - 899 (2007/10/02)
The catalytic hydrogenation of 1-(2-naphthyl)-2-alkylamino-1-propanones was investigated.During the hydrogenation of 1-(2-naphthyl)-2-alkylamino-1-propanones under pressure the unsubstituted naphthalene ring becomes saturated.
