130892-66-9 Usage
Uses
Used in Agricultural Applications:
2,6-Dichlorophenyl 3,4-dichlorophenyl ether is used as a herbicidal agent for the control of grasses and broadleaf weeds in crops such as soybeans, peanuts, and cotton. It operates by inhibiting the protoporphyrinogen oxidase enzyme in plants, which results in the accumulation of toxic compounds and leads to plant cell death, thereby protecting the growth of desired crops.
This application is crucial for maintaining crop health and yield, as the presence of weeds can compete with crops for nutrients, water, and sunlight, potentially reducing agricultural productivity. The use of oxyfluorfen helps to mitigate these issues, ensuring that crops can grow without competition from weeds.
While oxyfluorfen is considered to have low acute toxicity to mammals and is classified as a Group E chemical with no evidence of carcinogenicity in humans, it is important to manage its use responsibly. This is due to its potential persistence in the environment and the risk it may pose to aquatic organisms and non-target species. Proper application and adherence to guidelines can help minimize the environmental impact while maximizing the herbicidal benefits for agricultural productivity.
Check Digit Verification of cas no
The CAS Registry Mumber 130892-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,9 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130892-66:
(8*1)+(7*3)+(6*0)+(5*8)+(4*9)+(3*2)+(2*6)+(1*6)=129
129 % 10 = 9
So 130892-66-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H6Cl4O/c13-8-5-4-7(6-11(8)16)17-12-9(14)2-1-3-10(12)15/h1-6H
130892-66-9Relevant academic research and scientific papers
Synthesis, Structure Verification, and Chromatographic Relative Retention Times for Polychlorinated Diphenyl Ethers
Nevalainen, Tapio,Koistinen, Jaana,Nurmela, Pirjo
, p. 1341 - 1347 (2007/10/03)
Fifty-four polychlorinated diphenyl ether (PCDEs) congeners were synthesized, and their structures were confirmed by mass spectrometry and proton magnetic resonance spectroscopy. The gas chromatographic relative retention times (RRT) for the PCDEs were determined relative to a reference standard, -tetrachlorobiphenyl (PCB 77) on the fused silica capillary columns of SE-54 and OV-1701. The retention times for PCDEs increased with the increasing number of vicinal chlorines within a series of isomers. The chlorine substitution patterns of PCDEs were used to develop a method for predicting RRTs for congeners that were not synthesized.
