52448-15-4 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-2-AMINO-3-(5-CHLORO-1H-INDOL-3-YL)-PROPIONIC ACID is used as a key building block for the synthesis of peptide-based drugs and pharmaceuticals, leveraging its ability to modulate specific receptors and enzymes in the central nervous system.
Used in Neuroscience Research:
In the field of neuroscience, (S)-2-AMINO-3-(5-CHLORO-1H-INDOL-3-YL)-PROPIONIC ACID is utilized as a research compound to explore its interactions with the central nervous system, potentially leading to advancements in understanding and treating neurological conditions.
Used in Medicinal Chemistry:
(S)-2-AMINO-3-(5-CHLORO-1H-INDOL-3-YL)-PROPIONIC ACID is employed as a chiral compound in medicinal chemistry for the development of new therapeutic agents targeting the central nervous system, given its potential to modulate specific receptors and enzymes.
Used in Neurodegenerative Disease Treatment:
In the medical field, (S)-2-AMINO-3-(5-CHLORO-1H-INDOL-3-YL)-PROPIONIC ACID is being investigated for its potential use in the treatment of neurodegenerative diseases, due to its ability to modulate relevant biological targets and pathways.
Used in Mood Disorder Treatment:
(S)-2-AMINO-3-(5-CHLORO-1H-INDOL-3-YL)-PROPIONIC ACID is also being explored for its potential therapeutic effects in mood disorders, as its modulation of central nervous system receptors and enzymes may contribute to the management of such conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 52448-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,4 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52448-15:
(7*5)+(6*2)+(5*4)+(4*4)+(3*8)+(2*1)+(1*5)=114
114 % 10 = 4
So 52448-15-4 is a valid CAS Registry Number.
52448-15-4Relevant academic research and scientific papers
Syntheses of Substituted L- and D-Tryptophans
Irie, Kunihiko,Ishida, Akihiko,Nakamura, Tohru,Oh-ishi, Tokuro
, p. 2126 - 2139 (2007/10/02)
Several 5-substituted nb-methoxycarbonyl-L- and -D-tryptophan derivatives were synthesized from proline by a new route involving electrochemical oxidation, as well as by the known procedures.Removal of the Nb-methoxycarbonyl group was accomplished by treatment with Me3SiI in refluxing chloroform, then alkaline hydrolysis of the methyl esters afforded 5-substituted L- and D-tryptophans with high optical purities.Keywords - L-tryptophan 5-substituted; D-tryptophan 5-substituted; anodic oxidation; N-methoxycarbonyl group deprotection; Fischer indole synthesis; iodotrimethylsilane
