26477-34-9 Usage
Uses
Used in Pharmaceutical Synthesis:
2-methyl-3-nitro-1H-pyrrole is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with specific therapeutic properties.
Used in Organic Compounds Synthesis:
2-methyl-3-nitro-1H-pyrrole is also employed in the synthesis of a range of organic compounds, contributing to the diversity of chemical products and materials.
Used in Dye and Pigment Production:
2-methyl-3-nitro-1H-pyrrole serves as a precursor in the production of dyes and pigments, playing a crucial role in the coloration of various materials and products.
Used in Medicinal Chemistry Research:
Due to its potential biological activity, 2-methyl-3-nitro-1H-pyrrole is a subject of interest in medicinal chemistry research. It is studied for its possible applications in the development of new therapeutic agents and understanding its interaction with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 26477-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,7 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26477-34:
(7*2)+(6*6)+(5*4)+(4*7)+(3*7)+(2*3)+(1*4)=129
129 % 10 = 9
So 26477-34-9 is a valid CAS Registry Number.
26477-34-9Relevant academic research and scientific papers
Synthesis and nucleophilic properties of 1,2 -dialkyl-3-nitropyrroles and 1,5-dialkyl-4-nitropyrrole-2-carboxylic acid derivatives
Molins-Pujol, Antoni M.,Moranta, Concepcio,Arroyo, Carmina,Rodriguez, M. Teresa,Meca, M. Carmen,Pujol, M. Dolors,Bonal, Joaquim
, p. 2277 - 2289 (2007/10/03)
1,2-Dialkyl-3-nitropyrroles 1 are versatile synthetic tools for obtaining substituted pyrrolidines or fused ring heterocycles such as pyrrolopyridines, pyrrolopyrimidines or pyrroloazepines. We have established a method for obtaining compounds related to structure 1 and studied the reactivity as a nucleophile of the benzylic type moiety in the alkyl residue bound to position 2.
