259729-55-0 Usage
Uses
Used in Organic Synthesis:
Ethyl 3-(2-Pyridinyl)acrylate, N-Oxide is used as a key intermediate for the synthesis of various organic compounds. Its application in this field is due to its ability to participate in a range of chemical reactions, such as addition, substitution, and condensation reactions, which are essential for the formation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethyl 3-(2-Pyridinyl)acrylate, N-Oxide is used as a building block for the development of new drugs. Its unique chemical properties allow it to be incorporated into the molecular structure of potential therapeutic agents, contributing to their overall efficacy and selectivity.
Used in Chemical Research:
Ethyl 3-(2-Pyridinyl)acrylate, N-Oxide is also used in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. Its light yellow solid form makes it suitable for various analytical techniques, such as spectroscopy and chromatography, which are crucial for understanding its reactivity and potential applications.
Used in Material Science:
In the field of material science, Ethyl 3-(2-Pyridinyl)acrylate, N-Oxide can be used as a component in the development of novel materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with enhanced properties, such as improved stability, reactivity, or selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 259729-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,7,2 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 259729-55:
(8*2)+(7*5)+(6*9)+(5*7)+(4*2)+(3*9)+(2*5)+(1*5)=190
190 % 10 = 0
So 259729-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3/c1-2-14-10(12)7-6-9-5-3-4-8-11(9)13/h3-8H,2H2,1H3/b7-6+
259729-55-0Relevant academic research and scientific papers
Zhai, Ke,Lai, Miao,Wu, Zhiyong,Zhao, Mingqin,Jing, Yanqiu,Liu, Pengfei
, p. 20 - 26 (2018)
The systematic syntheses of 2-alkenylpyrazine N-oxides through palladium-catalyzed C-2 selective C–H olefination reaction was disclosed. Various acrylate esters substituted pyrazine N-oxides were obtained in up to 93% yields. Thermogravimetric analysis in
Palladium-catalyzed C-H functionalization of pyridine N-oxides: Highly selective alkenylation and direct arylation with unactivated arenes
Seung, Hwan Cho,Seung, Jun Hwang,Chang, Sukbok
supporting information; scheme or table, p. 9254 - 9256 (2009/02/03)
Two catalytic protocols of the oxidative C-C bond formation have been developed on the basis of the C-H bond activation of pyridine N-oxides. Pd-catalyzed alkenylation of the N-oxides proceeds with excellent regio-, stereo-, and chemoselectivity, and the
Stereoselective synthesis of swainsonines from pyridines
Heimg?rtner, Gerres,Raatz, Dirk,Reiser, Oliver
, p. 643 - 655 (2007/10/03)
An efficient synthesis of (-)-swainsonine and (-)-2,8a-di-epi-swainsonine was developed starting from readily available 2-pyridinecarbaldehyde and 3-hydroxypyridine. In particular, it was demonstrated that the mixture of simple indolizidines, i.e. lentigi
Asymmetric aminohydroxylation of heteroaromatic acrylates
Raatz, Dirk,Innertsberger, Clara,Reiser, Oliver
, p. 1907 - 1910 (2007/10/03)
N-, S- and O-heteroaromatic acrylates were aminohydroxylated with generally high regio- and enantioselectivity. While pyridylacrylates are not amenable towards this process, the corresponding N-oxides proved to be a useful substitute, allowing the access
