915375-27-8 Usage
Uses
Used in Pharmaceutical and Medicinal Chemistry Research:
(R)-tert-Butyl 1-oxo-1-(2-(pyridin-2-yl)hydrazinyl)propan-2-ylcarbamate is used as a research compound for the development of new drug candidates, specifically in the areas of antineoplastic, antiviral, and other therapeutic applications. Its unique structure and functional groups contribute to its potential as a promising candidate in these fields.
Used in Synthetic Organic Chemistry Research:
(R)-tert-Butyl 1-oxo-1-(2-(pyridin-2-yl)hydrazinyl)propan-2-ylcarbamate is used as a subject of study in synthetic organic chemistry due to its properties and reactivity. Researchers are interested in exploring its potential for the synthesis of new compounds and the development of novel synthetic pathways.
Used in Chemical Biology Research:
In the field of chemical biology, (R)-tert-Butyl 1-oxo-1-(2-(pyridin-2-yl)hydrazinyl)propan-2-ylcarbamate is used to investigate its interactions with biological systems. This research can provide insights into its potential applications in targeting specific biological processes or pathways, contributing to the advancement of drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 915375-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,3,7 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 915375-27:
(8*9)+(7*1)+(6*5)+(5*3)+(4*7)+(3*5)+(2*2)+(1*7)=178
178 % 10 = 8
So 915375-27-8 is a valid CAS Registry Number.
915375-27-8Relevant academic research and scientific papers
Convenient two-step preparation of [1,2,4]triazolo[4,3-a]pyridines from 2-hydrazinopyridine and carboxylic acids
Moulin, Aline,Martinez, Jean,Fehrentz, Jean-Alain
, p. 7591 - 7594 (2007/10/03)
Triazolopyridines are an important class of biologically active heterocyclic compounds. In this letter, we describe a new method for the synthesis of [1,2,4]triazolo[4,3-a]pyridines starting from 2-hydrazinopyridine and carboxylic acids. The resulting ace
