26906-40-1 Usage
Uses
Used in Plant Protection Agents:
Ethyl 2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate is used as a chemical component for the development of plant protection agents. It contributes to the formulation of products that protect plants from pests and diseases, ensuring a healthy and productive agricultural yield.
Used in Pharmaceuticals:
Ethyl 2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate is used as a building block in the synthesis of various pharmaceuticals. Its structure allows for the creation of new drug molecules with potential therapeutic applications, making it a valuable compound in the field of medicinal chemistry.
Used in Crop-Boosting Agrichemicals:
Ethyl 2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate is used as an active ingredient in agrichemicals designed to enhance crop growth and productivity. It may play a role in improving nutrient uptake, promoting plant health, and increasing resistance to environmental stressors, ultimately leading to higher crop yields.
Check Digit Verification of cas no
The CAS Registry Mumber 26906-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,0 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26906-40:
(7*2)+(6*6)+(5*9)+(4*0)+(3*6)+(2*4)+(1*0)=121
121 % 10 = 1
So 26906-40-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO3/c1-2-16-12(15)9-7-8-5-3-4-6-10(8)13-11(9)14/h3-6,9H,2,7H2,1H3,(H,13,14)
26906-40-1Relevant academic research and scientific papers
4-HYDROXY-2-QUINOLONES. 20. SYNTHESIS AND CHEMICAL CONVERSIONS OF ETHYL ESTERS OF CHLORO-SUBSTITUTED QUINOLINE-3-CARBOXYLIC ACIDS
Ukrainets, I. V.,Taran, S. G.,Gorokhova, O. V.,Marusenko, N. A.,Kovalenko, S. N.,et al.
, p. 167 - 175 (2007/10/03)
Preparative methods for the synthesis of ethyl esters of 2,4-dichloro- and 2-oxo-4-chloroquinoline-3-carboxylic acids were developed.The behavior of the compounds indicated was studied under conditions of alkaline and acidic hydrolysis, in reactions with some nucleophilic reagents, as well as in reductive dehalogenation.Results of the study of the antimicrobial and antiinflammatory activity of the synthesized compounds are presented.
