124499-29-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-PHENETHYL-PHENYL)-ETHYLAMINE HYDROCHLORIDE is used as a therapeutic agent for its potential role in the treatment of attention deficit hyperactivity disorder (ADHD) and mood disorders. Its influence on neurotransmitter release is believed to contribute to improvements in attention, focus, and emotional regulation.
Used in Neurological Research:
In the field of neuroscience, 2-(4-PHENETHYL-PHENYL)-ETHYLAMINE HYDROCHLORIDE serves as a research tool to better understand the mechanisms underlying mood regulation, attention, and sensory perception. Studying its effects on neurotransmitter release can provide insights into the development of novel treatments for neurological and psychiatric conditions.
Used in Dietary Supplements:
2-(4-PHENETHYL-PHENYL)-ETHYLAMINE HYDROCHLORIDE is utilized as an ingredient in dietary supplements, marketed to support cognitive function, mood enhancement, and increased energy levels. Its purported benefits are attributed to its influence on neurotransmitter release and potential impact on brain chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 124499-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,9 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124499-29:
(8*1)+(7*2)+(6*4)+(5*4)+(4*9)+(3*9)+(2*2)+(1*9)=142
142 % 10 = 2
So 124499-29-2 is a valid CAS Registry Number.
124499-29-2Relevant academic research and scientific papers
Highly Selective Adenosine A2 Receptor Agonists in a Series of N-Alkylated 2-Aminoadenosines
Francis, John E.,Webb, Randy L.,Ghai, Geetha R.,Hutchison, Alan J.,Moskal, Michael A.,et al.
, p. 2570 - 2579 (2007/10/02)
A wide variety of 2-substituted aminoadenosines were prepared for comparison with the moderately A2 receptor selective adenosine agonist 2-anilinoadenosine (CV-1808).High selectivity combined with significant affinity at the A2 receptor in rat membranes was observed for those amines bearing a two-carbon chain to which was attached an aryl, heteroaryl, or alicyclic moiety. 2-(2-Phenethylamino)adenosine (3d), a 14-fold A2 selective compound, was modified by introduction of a variety of substituents in the benzene ring and the side chain.Some of these changes led to improved A2 affinity and increased selectivity.Replacement of the phenyl moiety by cyclohexenyl produced a 210-fold selective agonist 3ag (CGS 22989) whereas the cyclohexanyl analogue 3af (CGS 22492) was 530-fold selective at the A2 site.These compounds showed hypotensive activity in rat models over a range of doses without the bradycardia observed with less selective agonists.
