92126-35-7 Usage
Uses
Used in Pharmaceutical Industry:
(2-phenyl-1,3-thiazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is used as an intermediate for the synthesis of pharmaceuticals, leveraging its carbamate functional group and the pharmacological properties of the thiazole ring to contribute to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, (2-phenyl-1,3-thiazole-4,5-diyl)dimethanediyl bis(methylcarbamate) is utilized as a pesticide or herbicide due to its carbamate functional group, which provides the necessary bioactivity for controlling pests and unwanted plant growth.
Used in Organic Synthesis:
(2-phenyl-1,3-thiazole-4,5-diyl)dimethanediyl bis(methylcarbamate) serves as a building block in organic synthesis, enabling the creation of a variety of organic compounds for different applications across various industries.
Used in Medicinal Chemistry:
This chemical compound is also used in medicinal chemistry for its potential applications, thanks to the presence of the thiazole ring, which is known for its pharmacological properties and can be harnessed in the design of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 92126-35-7 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 92126-35:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*3)+(1*5)=117
117 % 10 = 7
So 92126-35-7 is a valid CAS Registry Number.
92126-35-7Relevant 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.
