65638-91-7 Usage
Uses
Used in Pesticide Applications:
2,5-Cyclohexadien-1-imine, 4-[bis(pentachlorophenyl)methylene]-2,3,5,6-tetrachlorois used as an active ingredient in pesticides for controlling insects and pests in agricultural settings. Its effectiveness in this application is attributed to its ability to target and eliminate harmful organisms that can damage crops and reduce agricultural productivity.
Used in Agricultural Industry:
In the agricultural industry, 2,5-Cyclohexadien-1-imine, 4-[bis(pentachlorophenyl)methylene]-2,3,5,6-tetrachlorois used as a pesticide to protect crops from pests and insects. It is important to use this chemical with caution due to its potential environmental and health hazards, and to follow safety guidelines and regulations to minimize risks.
It is crucial to note that the use of this chemical should be carefully monitored and regulated to ensure that it does not cause harm to the environment, non-target organisms, or human health. This includes proper disposal, storage, and application methods to minimize the potential for contamination and exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 65638-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,3 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65638-91:
(7*6)+(6*5)+(5*6)+(4*3)+(3*8)+(2*9)+(1*1)=157
157 % 10 = 7
So 65638-91-7 is a valid CAS Registry Number.
65638-91-7Relevant academic research and scientific papers
Photochemistry and spectroscopy of "stable organic radicals": Steric and electronic effects in intermolecular photoinduced electron transfer
Canepa,Fox,Whitesell
, p. 3886 - 3892 (2007/10/03)
The intermolecular reactivities of amino-substituted perchlorotriphenylmethyl radicals 1-3 were studied, with particular emphasis on electron transfer (ET) reactions. The natural fluorescence lifetimes and the rates of the electron-transfer quenching were studied with several electron donors and acceptors. Fluorescence quenching studies demonstrate the importance of the redox potentials of the ET pair on the observed steric and electronic properties.
Inert Carbon Free Radicals. 3. Monofunctionalized Radicals from Perchlorotriphenylcarbenium Hexachloroantimonate
Ballester, Manuel,Riera, Juan,Castaner, Juan,Rodriguez, Antonio,Rovira, Concepcion,Veciana, Jaime
, p. 4498 - 4505 (2007/10/02)
Perchlorotriphenylcarbenium hexachloroantimonate (2) is prepared from perchlorotriphenylmethyl radical (PTM; 1) and SbCl5.Salt 2 by hydrolisis or ammonolysis yields perchlorofuchsone (3) or NH-tetradecachlorofuchsonimine (4), respectively, two quinonoid c
