92126-17-5 Usage
Description
[1-(3,4-dichlorophenyl)-1H-pyrazole-3,4-diyl]dimethanediyl bis(methylcarbamate) is a chemical compound featuring a pyrazole ring with two methylcarbamate groups attached. The presence of the dichlorophenyl group in the structure contributes to its effectiveness as a pesticide and insecticide, making it a potent agent for controlling various pests and insects. However, due to its potential toxicity to humans and the environment, it is essential to handle this compound with care and adhere to safety guidelines and regulations.
Uses
Used in Pesticide Industry:
[1-(3,4-dichlorophenyl)-1H-pyrazole-3,4-diyl]dimethanediyl bis(methylcarbamate) is used as an active ingredient in pesticides for controlling a wide range of pests and insects that can damage crops and gardens. Its effectiveness in killing insects is attributed to the dichlorophenyl group, which enhances the compound's insecticidal properties.
Used in Insecticide Industry:
In the insecticide industry, [1-(3,4-dichlorophenyl)-1H-pyrazole-3,4-diyl]dimethanediyl bis(methylcarbamate) is utilized as a key component in various formulations designed to eliminate insects that pose threats to human health or disrupt ecosystems. [1-(3,4-dichlorophenyl)-1H-pyrazole-3,4-diyl]dimethanediyl bis(methylcarbamate)'s ability to target and control insects makes it a valuable tool in this industry.
Check Digit Verification of cas no
The CAS Registry Mumber 92126-17-5 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, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 92126-17:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*1)+(1*7)=115
115 % 10 = 5
So 92126-17-5 is a valid CAS Registry Number.
92126-17-5Relevant articles and documents
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.