92126-29-9 Usage
General Description
"(1-phenyl-1H-1,2,3-triazole-4,5-diyl)dimethanediyl bis(methylcarbamate)" is a chemical compound that is used as a pesticide or insecticide. It is a carbamate derivative with two methylcarbamate groups linked to a central triazole ring. (1-phenyl-1H-1,2,3-triazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is used to control pests and insects in a variety of agricultural and industrial settings. It works by disrupting the nervous system of the pests, leading to their eventual death. However, it is important to handle this chemical with caution as it can be toxic to humans and other non-target organisms if not used properly. Proper safety measures and guidelines should be followed when handling and applying this chemical.
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 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.