73568-30-6 Usage
Description
2-CHLORO-7-METHYLSULFANYL-QUINOLINE-3-CARBALDEHYDE is a quinoline derivative with the molecular formula C12H8ClNO2S. It features a chloro group at the 2 position and a methylsulfanyl group at the 7 position, along with a carbaldehyde functional group at the 3 position. This chemical compound serves as a crucial intermediate or building block in the synthesis of various pharmaceuticals and agrochemicals, owing to its unique structure and functional groups.
Uses
Used in Pharmaceutical Industry:
2-CHLORO-7-METHYLSULFANYL-QUINOLINE-3-CARBALDEHYDE is used as an intermediate in the synthesis of specialized drugs. Its unique structure and functional groups make it a valuable starting material for the development of new pharmaceutical compounds.
Used in Agrochemical Industry:
2-CHLORO-7-METHYLSULFANYL-QUINOLINE-3-CARBALDEHYDE is also used as a building block in the production of agrochemicals. Its chemical properties allow it to be incorporated into the development of new pesticides and other agricultural products.
Check Digit Verification of cas no
The CAS Registry Mumber 73568-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,6 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73568-30:
(7*7)+(6*3)+(5*5)+(4*6)+(3*8)+(2*3)+(1*0)=146
146 % 10 = 6
So 73568-30-6 is a valid CAS Registry Number.
73568-30-6Relevant articles and documents
Synthesis and Herbicidal Activity of Triketone-Quinoline Hybrids as Novel 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors
Wang, Da-Wei,Lin, Hong-Yan,Cao, Run-Jie,Chen, Tao,Wu, Feng-Xu,Hao, Ge-Fei,Chen, Qiong,Yang, Wen-Chao,Yang, Guang-Fu
, p. 5587 - 5596 (2015/06/25)
4-Hydroxyphenylpyruvate dioxygenase (EC 1.13.11.27, HPPD) is one of the most important targets for herbicide discovery. In the search for new HPPD inhibitors with novel scaffolds, triketone-quinoline hybrids were designed and subsequently optimized on the basis of the structure-activity relationship (SAR) studies. Most of the synthesized compounds displayed potent inhibition of Arabidopsis thaliana HPPD (AtHPPD), and some of them exhibited broad-spectrum and promising herbicidal activity at the rate of 150 g ai/ha by postemergence application. Most promisingly, compound III-l, 3-hydroxy-2-(2-methoxy-7-(methylthio)quinoline-3-carbonyl)cyclohex-2-enone (Ki = 0.009 ～M, AtHPPD), had broader spectrum of weed control than mesotrione. Furthermore, compound III-l was much safer to maize at the rate of 150 g ai/ha than mesotrione, demonstrating its great potential as herbicide for weed control in maize fields. Therefore, triketone-quinoline hybrids may serve as new lead structures for novel herbicide discovery.
