2818-08-8 Usage
Uses
Used in Pharmaceutical Industry:
1H-Pyrrole-2,3-dicarboxylic acid dimethyl ester serves as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
As a building block in organic synthesis, 1H-Pyrrole-2,3-dicarboxylic acid dimethyl ester is utilized for the preparation of a wide range of bioactive compounds. Its versatility in chemical reactions enables the creation of diverse molecules with potential applications in various fields.
Used in Material Science:
1H-Pyrrole-2,3-dicarboxylic acid dimethyl ester has been studied for its potential use in the development of new materials. Its unique chemical properties make it a promising candidate for the creation of innovative materials with specific properties for various applications.
Used in Research and Development:
Due to its unique chemical properties, 1H-Pyrrole-2,3-dicarboxylic acid dimethyl ester is a valuable compound in research and development. It is used to explore new chemical reactions, synthesis pathways, and potential applications in various industries, including pharmaceuticals, materials science, and beyond.
Check Digit Verification of cas no
The CAS Registry Mumber 2818-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2818-08:
(6*2)+(5*8)+(4*1)+(3*8)+(2*0)+(1*8)=88
88 % 10 = 8
So 2818-08-8 is a valid CAS Registry Number.
2818-08-8Relevant academic research and scientific papers
Budzianowski, Jaromir
, p. 3299 - 3301 (1990)
A methanolic extract from leaves and flowers of Parietaria officinalis afforded three acids, namely caffeoylmalic, 1H-pyrrole-2,3-dicarboxylic and 1--1H-pyrrole-2,3,5-tricarboxylic.
Lithiations of 1-Trialkylsilylpyrroles: N to C Silyl Group Rearrangement
Chadwick, Derek J.,Hodgson, Simon T.
, p. 1833 - 1836 (2007/10/02)
The sites of metallation with alkyl-lithium reagents of 1-trimethylsilyl- and 1-triethylsilyl-pyrroles have been explored under a variety of conditions.With short reaction times, BunLi reacts with 1-trimethylsilylpyrrole in hexane predominantly at the 2-position though with ButLi in pentane the unusual 3-metallated product is preferred.During prolonged reaction of 1-trimethylsilyl- and 1-triethylsilyl-pyrroles with ButLi, the 2-monolithio- and the 2,4- and 2,5-dilithio-intermediates are formed, in which, unexpectedly, the silyl groups migrate to the pyrrole 2-position.Under conditions favouring enhanced ionicity, BunLi cleaves the N-SiMe3 bond in preference to ring metallation.
