1006694-45-6 Usage
Description
(2E)-2-cyano-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide is a chemical compound with the molecular formula C15H10N4OS. It is a derivative of thiazole and is classified as an enamide. (2E)-2-cyano-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide features a cyano group and a thiazole moiety, which may contribute to its potential biological activity. Thiazoles are known for their antimicrobial, antiparasitic, and anticancer properties, while cyano groups can act as electron-withdrawing groups in organic chemistry. The chemical structure of (2E)-2-cyano-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide suggests that it may have potential pharmaceutical applications and could be further studied for its medicinal properties.
Uses
Used in Pharmaceutical Industry:
(2E)-2-cyano-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide is used as a potential pharmaceutical candidate for various applications due to its unique chemical structure and the presence of biologically active functional groups. Its thiazole moiety is known to possess antimicrobial, antiparasitic, and anticancer properties, which could be harnessed for the development of new drugs targeting these areas. Additionally, the cyano group may contribute to its electron-withdrawing properties, further enhancing its potential as a pharmaceutical agent.
Used in Medicinal Chemistry Research:
(2E)-2-cyano-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide is used as a subject of study in medicinal chemistry research to explore its potential applications and properties. Researchers may investigate its interactions with biological targets, its ability to modulate specific pathways, and its potential synergistic effects with other compounds. This could lead to the discovery of new therapeutic agents or the improvement of existing ones.
Used in Drug Design and Development:
(2E)-2-cyano-3-phenyl-N-(1,3-thiazol-2-yl)prop-2-enamide is used as a starting point in drug design and development processes. Its unique structure and functional groups can be further modified or optimized to enhance its biological activity, selectivity, and pharmacokinetic properties. This may involve the synthesis of analogs, structure-activity relationship studies, and computational modeling to predict and improve its performance as a drug candidate.
Check Digit Verification of cas no
The CAS Registry Mumber 1006694-45-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,6,9 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1006694-45:
(9*1)+(8*0)+(7*0)+(6*6)+(5*6)+(4*9)+(3*4)+(2*4)+(1*5)=136
136 % 10 = 6
So 1006694-45-6 is a valid CAS Registry Number.
1006694-45-6Relevant articles and documents
N-hetaryl-2-cyanoacetamides in the synthesis of substituted (E)-N-hetaryl-2-cyanoacrylamides, (E)-N-alkyl-N-hetaryl-2-cyanoacrylamides, and 6-amino-2-oxo-4-phenyl-1-(pyridin-2-yl)-1,2-dihydropyridine-3,5-dicarbonitriles
Dyachenko,Dyachenko,Rusanov
, p. 83 - 89 (2007)
Knoevenagel condensation of N-hetaryl-substituted cyanoacetamides with aldehydes gave the corresponding (E)-N-hetaryl-2-cyanoacrylamides which were converted into (E)-N-alkyl-N-hetaryl-2-cyanoacrylamides and 6-amino-2-oxo-4- phenyl-1-(pyridin-2-yl)-1,2-dihydropyridine-3,5-dicarbonitriles. The structure of (E)-N-(pyridin-2-yl)-2-cyano-3-phenylprop-2-enamide was determined by X-ray analysis.
