184476-69-5 Usage
Complex structure
The compound has a multi-layered structure featuring an indole ring, two acetyl groups, a substituted pyridine ring, and a phenylmethyl group.
Indole derivative
It is a modified version of the 1H-Indole core structure, with additional functional groups attached to it.
药理研究常用
Commonly used in pharmaceutical research and drug development due to its potential as a therapeutic agent.
独特结构
The unique structure of the compound makes it a promising candidate for the development of new drugs and treatments.
生物学性质尚在研究
Its specific pharmacological and biological properties are still being studied, indicating that more research is needed to fully understand its potential applications in the field of medicine.
乙酰基团
The presence of two acetyl groups in the structure may contribute to its biological activity and potential therapeutic applications.
吡啶环取代
The compound features a substituted pyridine ring, which may influence its binding affinity and selectivity for various biological targets.
苯甲基基团
The phenylmethyl group attached to the compound may contribute to its lipophilicity and ability to cross cell membranes, potentially affecting its pharmacokinetic and pharmacodynamic properties.
药物开发潜力
The compound's potential applications in the field of medicine are still being explored, and further research is needed to fully understand its capabilities as a therapeutic agent.
Check Digit Verification of cas no
The CAS Registry Mumber 184476-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,4,7 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 184476-69:
(8*1)+(7*8)+(6*4)+(5*4)+(4*7)+(3*6)+(2*6)+(1*9)=175
175 % 10 = 5
So 184476-69-5 is a valid CAS Registry Number.
184476-69-5Relevant academic research and scientific papers
Bennasar, M.-Lluisa,Jimenez, Juan-Miguel,Sufi, Bilal A.,Bosch, Joan
, p. 7653 - 7656 (1996)
1,4-Dihydropyridines 3 resulting from the addition of the enolate derived from 1-acetylindole (1) to pyridinium salts 2 do not undergo cyclization under the usual acidic conditions, but do satisfactorily cyclize to the tetracyclic derivatives 4 by treatment with TsOH in the presence of lithium iodide.
