19056-82-7 Usage
Description
Diethyl [(2,5-dichlorophenyl)amino]methylidenepropanedioate is a chemical compound with the molecular formula C14H16Cl2N2O4. It is an organic compound that belongs to the dithiophenate family. Its molecular structure features two diethyl ester groups attached to a central propanedioate scaffold, which is connected to a 2,5-dichlorophenyl group. diethyl [(2,5-dichlorophenyl)amino]methylidenepropanedioate is commonly used as a pesticide and insecticide due to its broad-spectrum activity against various agricultural pests, making it a valuable tool for crop protection.
Uses
Used in Agricultural Industry:
Diethyl [(2,5-dichlorophenyl)amino]methylidenepropanedioate is used as a pesticide and insecticide for its broad-spectrum activity against a variety of agricultural pests. Its application helps in protecting crops from damage caused by these pests, ensuring a healthy and productive agricultural yield.
However, due to its potential toxicity and environmental impact, careful handling and application of diethyl [(2,5-dichlorophenyl)amino]methylidenepropanedioate are crucial to minimize negative effects on non-target organisms and ecosystems. This includes adhering to recommended application rates, timing, and methods to reduce the risk of exposure to humans, wildlife, and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 19056-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,5 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19056-82:
(7*1)+(6*9)+(5*0)+(4*5)+(3*6)+(2*8)+(1*2)=117
117 % 10 = 7
So 19056-82-7 is a valid CAS Registry Number.
19056-82-7Relevant articles and documents
An NMR study of halogenated 1,4-dihydro-1-ethyl-4-oxoquinoline-3-carboxylates
Podanyi, Benjamin,Kereszturi, Geza,Vasvari-Debreczy, Lelle,Chinoin, Istvan Hermecz,Toth, Gabor
, p. 972 - 978 (2007/10/03)
Ethyl 1,4-dihydro-1-ethyl-4-oxoquinoline-3-carboxylate and 29 of its mono-, di-and tri-fluoro and/or -chloro derivatives were synthesized and their 1H, 13C and 19F NMR spectra were recorded. 1H, 13C and 19F chemical shifts, JHH, JFH, JCF and JFF coupling constants are reported. The 13C substituent chemical shift values of the chloro and fluoro substituents were calculated by linear multiple regression.