6525-46-8 Usage
Uses
Used in Pharmaceutical Research and Development:
5-NITRO-DL-TRYPTOPHAN is used as a key intermediate in the synthesis of various pharmaceutical compounds for the development of antibiotics and anti-tumor agents. Its unique properties allow for the creation of novel drug candidates with potential therapeutic benefits.
Used in Neuroscience Research:
In the field of neuroscience, 5-NITRO-DL-TRYPTOPHAN is utilized as a research tool to study its effects on neurotransmitter levels in the brain. This can contribute to a better understanding of neurological disorders and the development of new treatments for such conditions.
Used in Chemical Synthesis:
5-NITRO-DL-TRYPTOPHAN serves as a building block in the synthesis of complex organic compounds, which can be applied in various chemical and industrial processes. Its unique structure makes it a valuable component in the creation of new chemical entities with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6525-46-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,2 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6525-46:
(6*6)+(5*5)+(4*2)+(3*5)+(2*4)+(1*6)=98
98 % 10 = 8
So 6525-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3O4/c12-9(11(15)16)3-6-5-13-10-2-1-7(14(17)18)4-8(6)10/h1-2,4-5,9,13H,3,12H2,(H,15,16)
6525-46-8Relevant 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
