92126-33-5 Usage
Uses
Used in Agricultural Industry:
(3-phenyl-1,2-thiazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is used as an insecticide for controlling a variety of pests in crops and gardens. It works by inhibiting the activity of cholinesterase, an enzyme responsible for nerve signal transmission, leading to paralysis and eventual death of the insects.
However, it is important to note that (3-phenyl-1,2-thiazole-4,5-diyl)dimethanediyl bis(methylcarbamate) poses a potential risk to human health and the environment. It can be harmful if swallowed, inhaled, or absorbed through the skin, and it may also persist in the environment and harm non-target organisms. As a result, the use of this chemical is closely regulated, and it is crucial to handle it with care and follow safety guidelines to minimize potential exposure and harm.
Check Digit Verification of cas no
The CAS Registry Mumber 92126-33-5 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, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92126-33:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*3)+(1*3)=115
115 % 10 = 5
So 92126-33-5 is a valid CAS Registry Number.
92126-33-5Relevant 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.
