313490-90-3 Usage
Uses
Used in Organic Synthesis:
Ethyl 2-((tert-butoxycarbonyl)amino)-2-(pyridin-2-yl)acetate is used as a key intermediate for the synthesis of other organic compounds, leveraging its reactivity and structural components to facilitate the formation of desired products in chemical reactions.
Used in Chemical Reactions as a Reagent:
In the realm of organic chemistry experiments, ethyl 2-((tert-butoxycarbonyl)amino)-2-(pyridin-2-yl)acetate serves as a reagent, enabling chemists to explore and execute a variety of chemical transformations, including the formation and modification of carbamates and other functional groups.
Used in Research and Development:
Ethyl 2-((tert-butoxycarbonyl)amino)-2-(pyridin-2-yl)acetate is utilized in research settings to study its chemical properties and potential applications, contributing to the advancement of organic chemistry and the discovery of new synthetic pathways and compounds.
Used in Pharmaceutical Industry:
As a component in the synthesis of pharmaceuticals, ethyl 2-((tert-butoxycarbonyl)amino)-2-(pyridin-2-yl)acetate may be used as a building block for the development of new drugs, taking advantage of its unique structural elements to create molecules with specific therapeutic properties.
Used in Solvent Applications:
Given its ester nature, ethyl 2-((tert-butoxycarbonyl)amino)-2-(pyridin-2-yl)acetate may also find use as a solvent in certain chemical processes, where its solubility properties can be exploited to dissolve other compounds or facilitate reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 313490-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,4,9 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 313490-90:
(8*3)+(7*1)+(6*3)+(5*4)+(4*9)+(3*0)+(2*9)+(1*0)=123
123 % 10 = 3
So 313490-90-3 is a valid CAS Registry Number.
313490-90-3Relevant academic research and scientific papers
Shi, Yi,Gulevich, Anton V.,Gevorgyan, Vladimir
, p. 14191 - 14195 (2014)
A general and efficient NH insertion reaction of rhodium pyridyl carbenes derived from pyridotriazoles was developed. Various NH-containing compounds, including amides, anilines, enamines, and aliphatic amines, smoothly underwent the NH insertion reaction to afford 2-picolylamine derivatives. The developed transformation was further utilized in a facile one-pot synthesis of imidazo[1,5-a]pyridines.
