92126-24-4 Usage
Uses
Used in Agricultural Industry:
[1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3,4-diyl]dimethanediyl bis(methylcarbamate) is used as an insecticide for controlling a wide range of pests. Its application reason is the inhibition of the acetylcholinesterase enzyme, which is crucial for the nervous system's proper functioning in insects. By disrupting this enzyme's activity, the compound effectively kills or incapacitates the targeted pests, protecting crops and increasing agricultural productivity.
Safety and Environmental Considerations:
It is essential to use [1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3,4-diyl]dimethanediyl bis(methylcarbamate) with caution and adhere to safety guidelines. [1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3,4-diyl]dimethanediyl bis(methylcarbamate) can have toxic effects on non-target organisms and may pose risks to human health and the environment if not handled and applied correctly. Proper management and application techniques are crucial to minimize potential adverse effects and ensure the sustainability of agricultural practices.
Check Digit Verification of cas no
The CAS Registry Mumber 92126-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,2 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92126-24:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*2)+(1*4)=114
114 % 10 = 4
So 92126-24-4 is a valid CAS Registry Number.
92126-24-4Relevant academic research and scientific papers
Synthesis and evaluation of furan, thiophene, and azole bis[(carbamoyloxy)methyl] derivatives as potential antineoplastic agents
Anderson,Jones
, p. 1559 - 1565 (2007/10/02)
A series of bis(hydroxymethyl)-substituted heterocycles were synthesized and converted to the corresponding bis(methylcarbamate) derivatives. The heterocyclic systems studied were based on 2-phenyl-3-methylfuran, 1-phenylpyrazole, 1-phenyl-5-methylpyrazole, 1-phenyl-5-methylthiopene, 1-phenyl-1,2,3-triazole, 3-phenylisoxazole, 3-phenylisothiazole, 2-phenylthiazole, and 2-phenyloxazole. None of the bis(carbamates) prepared was active against murine P388 lymphocytic leukemia. Pyrrole bis(carbamate), which exhibited antileukemic activity, also showed reactivity toward 4-(p-nitrobenzyl)pyridine while the inactive bis(carbamates) were unreactive in the 4-(p-nitrobenzyl)pyridine assay.
