103394-76-9 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
2-AMINO-3-PYRIDIN-2-YL-PROPIONIC ACID ETHYL ESTER is utilized as a key intermediate in the synthesis of various biologically active compounds, contributing to the development of new drugs with potential applications in treating a wide array of conditions.
Used in Organic Chemistry:
In the realm of organic chemistry, 2-AMINO-3-PYRIDIN-2-YL-PROPIONIC ACID ETHYL ESTER serves as a reagent, particularly instrumental in the formation of peptide and amide bonds, which are fundamental in the construction of complex organic molecules and biologically relevant compounds.
Used in Anti-inflammatory Applications:
2-AMINO-3-PYRIDIN-2-YL-PROPIONIC ACID ETHYL ESTER may be employed as an anti-inflammatory agent, leveraging its pharmacological properties to modulate inflammatory responses and alleviate symptoms associated with inflammation.
Used in Analgesic Applications:
As an analgesic, 2-AMINO-3-PYRIDIN-2-YL-PROPIONIC ACID ETHYL ESTER could be used to develop pain-relieving medications, offering an alternative or adjunct to existing analgesics for the management of acute and chronic pain conditions.
Used in Anti-cancer Applications:
2-AMINO-3-PYRIDIN-2-YL-PROPIONIC ACID ETHYL ESTER holds promise as an anti-cancer agent, potentially contributing to the development of novel therapeutics that target various types of cancer through its inherent pharmacological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 103394-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,9 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103394-76:
(8*1)+(7*0)+(6*3)+(5*3)+(4*9)+(3*4)+(2*7)+(1*6)=109
109 % 10 = 9
So 103394-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O2/c1-2-14-10(13)9(11)7-8-5-3-4-6-12-8/h3-6,9H,2,7,11H2,1H3
103394-76-9Relevant articles and documents
OX2R COMPOUNDS
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Paragraph 0475; 0476; 0516; 0518, (2019/10/19)
Methods and compositions for agonizing a type-2 orexin receptor (OX2R) in a cell determined to be in need thereof, including the general method of (a) administering to a subject a cyclic guanidinyl OX2R agonist and (b) detecting a resultant enhanced wakefulness or increased resistance to diet-induced accumulation of body fat, or abbreviated recovery from general anesthesia or jet lag.
IMIDAZOPYRAZINE DERIVATIVES, PROCESS FOR PREPARATION THEREOF, AND THEIR USES AS LUCIFERINS
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Page/Page column 60; 62, (2018/11/22)
The present invention is in the field of bioluminescence in biology and/or medicine. In particular, the invention provides imidazopyrazine derivatives, processes for preparation thereof, and their uses as luciferins.
Unnatural α-amino ethyl esters from diethyl malonate or ethyl β-bromo-α-hydroxyiminocarboxylate
Coutant, Eloi P.,Hervin, Vincent,Gagnot, Glwadys,Ford, Candice,Baatallah, Racha,Janin, Yves L.
supporting information, p. 2853 - 2860 (2018/11/26)
We have explored here the scope of the age-old diethyl malonate-based accesses to α-amino esters involving Knoevenagel condensations of diethyl malonate on aldehydes, reductions of the resulting alkylidenemalonates, the preparation of the corresponding α-hydroxyimino esters and their final reduction. This synthetic pathway turned out to be general although some unexpected limitations were encountered. The synthetic modifications of some of the intermediates - using Suzuki-Miyaura coupling or cycloadditions - before undertaking the oximation step - provided accesses to further α-amino esters. Moreover, other pathways to α-hydroxyimino esters were explored including an attempt to improve the cycloadditions between ethyl β-bromo-α-hydroxyiminocarboxylate and various alkylfuranes.
