247259-31-0 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 2-(piperidin-3-yl)acetate hydrochloride is used as a research chemical for the development of new drugs and therapies. Its structural similarity to Methylphenidate, a known CNS stimulant, makes it a valuable compound for studying the effects of stimulants on the central nervous system and potentially developing new treatments for conditions such as attention deficit hyperactivity disorder (ADHD) and narcolepsy.
Used in Research and Development:
Methyl 2-(piperidin-3-yl)acetate hydrochloride is used as a research tool in the field of medicinal chemistry and neuroscience. Its unique structure allows scientists to investigate the mechanisms of action of CNS stimulants and explore the potential for developing new drugs with improved efficacy and reduced side effects.
Used in Drug Synthesis:
Methyl 2-(piperidin-3-yl)acetate hydrochloride can be used as an intermediate in the synthesis of other pharmaceutical compounds. Its functional groups and structural features make it a versatile building block for the development of new drugs with potential applications in various therapeutic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 247259-31-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,2,5 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 247259-31:
(8*2)+(7*4)+(6*7)+(5*2)+(4*5)+(3*9)+(2*3)+(1*1)=150
150 % 10 = 0
So 247259-31-0 is a valid CAS Registry Number.
InChI:InChI=1S/C8H15NO2.ClH/c1-11-8(10)5-7-3-2-4-9-6-7;/h7,9H,2-6H2,1H3;1H
247259-31-0Relevant articles and documents
Synthesis and Pharmacology of Site-Specific Cocaine Abuse Treatment Agents: The Role of the Phenyl Group in Highly Modified Methylphenidate analogs as Dopamine Uptake Inhibitors
Deutsch, Howard M.,Dunn, Travis,Ye, Xiaocong,Schweri, Margaret M.
, p. 213 - 222 (2007/10/03)
A series of modified methylphenidate derivatives was synthesized and tested for inhibitory potency in [3H]WIN 35,428 binding and [3H]dopamine uptake assays using rat striatal tissue. In these compounds the role of the phenyl ring was investigated by its r