65423-11-2 Usage
Uses
Used in Medicinal Chemistry:
2-(4-butoxyphenyl)ethanamine is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new medications.
Used in Drug Development:
2-(4-butoxyphenyl)ethanamine serves as a building block in the creation of psychoactive substances, playing a crucial role in advancing our understanding of their effects on the human body.
Used in Neuroscience Research:
2-(4-butoxyphenyl)ethanamine is utilized as a research tool to study the central nervous system, potentially leading to breakthroughs in the treatment of neurological disorders.
Used in Pharmacology Research:
2-(4-butoxyphenyl)ethanamine is employed in pharmacological studies to investigate its interactions with the body's physiological processes, which may help in designing more effective therapeutic strategies.
It is essential to handle 2-(4-butoxyphenyl)ethanamine with care and adhere to safety protocols and regulations to ensure safe usage in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 65423-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,2 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65423-11:
(7*6)+(6*5)+(5*4)+(4*2)+(3*3)+(2*1)+(1*1)=112
112 % 10 = 2
So 65423-11-2 is a valid CAS Registry Number.
65423-11-2Relevant academic research and scientific papers
Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties
Freudenreich, Charles,Samama, Jean-Pierre,Biellmann, Jean-Francois
, p. 3344 - 3353 (2007/10/02)
Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.
