92126-29-9 Usage
Uses
Used in Agricultural Industry:
(1-phenyl-1H-1,2,3-triazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is used as a pesticide for controlling a broad spectrum of pests and insects that can damage crops and reduce agricultural yields. Its effectiveness stems from its ability to disrupt the nervous systems of pests, leading to their eventual death and protecting the crops from destruction.
Used in Industrial Settings:
In industrial settings, (1-phenyl-1H-1,2,3-triazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is used as an insecticide to manage insect infestations that can cause structural damage or pose health risks. By targeting the insects' nervous systems, this chemical compound helps to eliminate infestations and maintain a safe and productive environment.
Safety Precautions:
Given its potent insecticidal properties, it is crucial to handle (1-phenyl-1H-1,2,3-triazole-4,5-diyl)dimethanediyl bis(methylcarbamate) with care to avoid toxicity to humans and other non-target organisms. Adhering to proper safety measures and guidelines is essential when applying this chemical to ensure the well-being of both people and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 92126-29-9 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 92126-29:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*2)+(1*9)=119
119 % 10 = 9
So 92126-29-9 is a valid CAS Registry Number.
92126-29-9Relevant 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.
