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(3-phenyl-1,2-oxazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is a carbamate compound with the molecular formula C20H18N4O6. It is characterized by its ability to inhibit the activity of the enzyme acetylcholinesterase, which plays a crucial role in the breakdown of the neurotransmitter acetylcholine.
Used in Pesticide Industry:
(3-phenyl-1,2-oxazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is used as a pesticide and insecticide for its effectiveness in controlling and eliminating various pests. (3-phenyl-1,2-oxazole-4,5-diyl)dimethanediyl bis(methylcarbamate)'s ability to inhibit acetylcholinesterase leads to the buildup of acetylcholine in the nervous system of the target pests, causing overstimulation of nerves and muscles, ultimately resulting in paralysis and death.
Used in Agricultural Applications:
In the agricultural sector, (3-phenyl-1,2-oxazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is employed to protect crops from pests and ensure a healthy yield. Its use helps minimize the damage caused by insects, contributing to increased productivity and better crop quality.
Used in Public Health and Sanitation:
(3-phenyl-1,2-oxazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is also utilized in public health and sanitation efforts to control disease-carrying insects, such as mosquitoes and flies. By reducing the populations of these pests, the spread of diseases can be effectively managed and prevented.

92126-31-3

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92126-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92126-31-3 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 92126-31:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*3)+(1*1)=113
113 % 10 = 3
So 92126-31-3 is a valid CAS Registry Number.

92126-31-3Downstream Products

92126-31-3Relevant 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.

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