56164-43-3 Usage
Uses
Used in Pharmaceutical and Medical Research:
2-forMyl-1H-Pyrrole-3-carbonitrile is used as a building block for synthesizing bioactive compounds and potential drugs due to its versatile nature and demonstrated biological activities.
Used in Anticancer Applications:
In the field of oncology, 2-forMyl-1H-Pyrrole-3-carbonitrile is utilized as an anticancer agent, contributing to the development of new therapeutic strategies against various types of cancer.
Used in Antibacterial Applications:
2-forMyl-1H-Pyrrole-3-carbonitrile is employed as an antibacterial agent, highlighting its potential in addressing bacterial infections and contributing to the discovery of new antimicrobial drugs.
Used in Antifungal Applications:
In the realm of antifungal therapy, 2-forMyl-1H-Pyrrole-3-carbonitrile is used to combat fungal infections, showcasing its broad-spectrum activity and potential in developing novel antifungal medications.
Used in Drug Development:
2-forMyl-1H-Pyrrole-3-carbonitrile is used as a subject of interest in drug development, given its potential therapeutic applications and the ongoing research into its properties and effects.
Used in Medicinal Chemistry Research:
2-forMyl-1H-Pyrrole-3-carbonitrile is also used in medicinal chemistry research to explore its chemical properties, mechanisms of action, and to identify new drug candidates based on its structure and activity.
Check Digit Verification of cas no
The CAS Registry Mumber 56164-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,6 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56164-43:
(7*5)+(6*6)+(5*1)+(4*6)+(3*4)+(2*4)+(1*3)=123
123 % 10 = 3
So 56164-43-3 is a valid CAS Registry Number.
56164-43-3Relevant academic research and scientific papers
Synthesis of 2,3-dicarbonylated pyrroles and furans via the three-component Hantzsch reaction
Moss, Thomas A.,Nowak, Thorsten
experimental part, p. 3056 - 3060 (2012/08/08)
Pyrroles containing a 2,3-dicarbonyl substitution pattern are synthesized in one step via a three-component Hantzsch procedure. The normally difficult-to-access substrates are readily obtained in short reaction times and in moderate to good yields, giving pharmaceutically attractive products containing multiple handles for further elaboration.
