97580-57-9 Usage
Description
1-(2-Chloro-pyridin-3-yl)-1H-pyrrole-2-carbaldehyde is a chemical compound characterized by the molecular formula C11H8ClNO. It is a derivative of pyrrole, featuring a pyridine ring with an attached chlorine atom and a carbaldehyde group. 1-(2-Chloro-pyridin-3-yl)-1H-pyrrole-2-carbaldehyde is recognized for its significance in organic synthesis and medicinal chemistry, where it serves as a fundamental building block for creating biologically active molecules and pharmaceutical drugs. Furthermore, it has garnered interest for its potential application as a fluorescent probe for detecting metal ions in biological systems, highlighting its utility in research and various industrial applications.
Uses
Used in Organic Synthesis:
1-(2-Chloro-pyridin-3-yl)-1H-pyrrole-2-carbaldehyde is utilized as a key intermediate in the synthesis of complex organic molecules. Its unique structural features, including the pyridine ring and the carbaldehyde group, enable the formation of a wide range of chemical products with diverse applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(2-Chloro-pyridin-3-yl)-1H-pyrrole-2-carbaldehyde is employed as a building block for the development of biologically active molecules and pharmaceutical drugs. Its structural versatility allows for the design and synthesis of novel compounds with potential therapeutic applications.
Used as a Fluorescent Probe in Biological Systems:
1-(2-Chloro-pyridin-3-yl)-1H-pyrrole-2-carbaldehyde has been investigated for its potential use as a fluorescent probe for detecting metal ions in biological systems. Its ability to interact with metal ions and exhibit fluorescence upon binding makes it a valuable tool for research in biochemistry and molecular biology.
Used in Research and Industrial Applications:
The chemical properties of 1-(2-Chloro-pyridin-3-yl)-1H-pyrrole-2-carbaldehyde make it suitable for various research and industrial applications. Its versatility in forming different chemical products and its potential as a fluorescent probe contribute to its wide-ranging utility in these domains.
Check Digit Verification of cas no
The CAS Registry Mumber 97580-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,8 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97580-57:
(7*9)+(6*7)+(5*5)+(4*8)+(3*0)+(2*5)+(1*7)=179
179 % 10 = 9
So 97580-57-9 is a valid CAS Registry Number.
