124499-27-0 Usage
Uses
Used in Research and Pharmaceutical Applications:
2-(4-STYRYL-PHENYL)-ETHYLAMINE HYDROCHLORIDE is used as a research chemical for the synthesis of organic compounds and the development of new drugs. Its unique structure and properties make it a valuable tool in the advancement of pharmaceutical research.
Used in Chemical Reactions:
In the Chemical Industry, 2-(4-STYRYL-PHENYL)-ETHYLAMINE HYDROCHLORIDE is used as a reagent in various chemical reactions. Its ability to participate in a range of reactions contributes to the synthesis of new compounds and the modification of existing ones.
Used in Organic Chemistry:
2-(4-STYRYL-PHENYL)-ETHYLAMINE HYDROCHLORIDE serves as a building block in organic chemistry, enabling the creation of complex molecular structures. Its versatility in forming different types of chemical bonds makes it an essential component in the design and synthesis of novel organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 124499-27-0 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 124499-27:
(8*1)+(7*2)+(6*4)+(5*4)+(4*9)+(3*9)+(2*2)+(1*7)=140
140 % 10 = 0
So 124499-27-0 is a valid CAS Registry Number.
124499-27-0Relevant 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.
