13315-77-0 Usage
Molecular Structure
The compound consists of a pyrrole ring with two carboxylic acid groups at the 3 and 4 positions, as well as three phenyl groups at the 1, 2, and 5 positions, and a diethyl ester group.
Esterification
The compound is formed by the esterification of 1,2,5-triphenylpyrrole-3,4-dicarboxylic acid with diethyl alcohol.
Usage
It is commonly used in organic synthesis and pharmaceutical research due to its potential biological activities.
Biological Activities
It has been studied for its antioxidant, anti-inflammatory, and anticancer properties.
Potential in Neurodegenerative Diseases
The compound has shown potential in the treatment of neurodegenerative diseases.
Further Research
Further research is needed to better understand its full range of applications and potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 13315-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,1 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13315-77:
(7*1)+(6*3)+(5*3)+(4*1)+(3*5)+(2*7)+(1*7)=80
80 % 10 = 0
So 13315-77-0 is a valid CAS Registry Number.
13315-77-0Relevant academic research and scientific papers
Chuang, Che-Ping,Wu, Yi-Lung
, p. 1841 - 1847 (2004)
Oxidative free radical reactions of enamino esters are described. Electrophilic carbon-centered radicals produced by the cerium(IV) ammonium nitrate (CAN) oxidation of β-dicarbonyl compounds undergo efficient addition to the C-C double bond of enamino est
Electrochemical Oxidative Cyclization: Synthesis of Polysubstituted Pyrrole from Enamines
Chen, Zhiwei,Shi, Guang,Tang, Wei,Sun, Jie,Wang, Wenxing
, p. 951 - 955 (2021/02/03)
A conceptually novel method for the preparation of pyrrole is described by electrochemical-oxidation-induced intermolecular annulation via enamines. In a simple undivided cell, based on a sodium acetate-facilitated, polysubstituted pyrrole derivations has been facilely synthesized under external oxidant-free condition. This electrosynthetic approach providing an environmentally benign protocol for C?C bond cross-coupling and oxidative annulation, which features unparalleled broad scope of substrates and practicality.
