178430-92-7 Usage
Derivative of 1,2,5-oxadiazole
Yes
It is a modified version of the parent compound 1,2,5-oxadiazole, which is a five-membered heterocycle containing two nitrogen atoms and one oxygen atom.
Presence of ethoxy group
Yes
The compound contains an ethoxy (-OCH2CH3) group, which is an ether functional group derived from ethanol.
Presence of phenyl group
Yes
The compound features a phenyl group (C6H5), which is a benzene ring with one hydrogen atom replaced by the oxadiazole ring.
Classification
Oxide
It is classified as an oxide due to the presence of oxygen atoms in its molecular structure.
Application in pharmaceutical and medicinal research
Yes
The compound is used in the development and study of potential biological activities, which may lead to the discovery of new drugs or therapies.
Utilization in organic synthesis
Yes
It serves as a building block or intermediate in the synthesis of various organic compounds.
Development of functional materials
Yes
The compound can be used to create new materials with specific properties for various applications.
Chemical and physical properties
Interesting
The compound exhibits unique chemical and physical properties that make it a subject of interest for further investigation and potential applications in different fields.
Potential applications
Various fields
Due to its unique properties and structure, the compound may find applications in a wide range of fields, including pharmaceuticals, materials science, and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 178430-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,4,3 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 178430-92:
(8*1)+(7*7)+(6*8)+(5*4)+(4*3)+(3*0)+(2*9)+(1*2)=157
157 % 10 = 7
So 178430-92-7 is a valid CAS Registry Number.
178430-92-7Relevant academic research and scientific papers
Unsymmetrically substituted furoxans. Part 16 [1]. Reaction of benzenesulfonyl substituted furoxans with ethanol and ethanethiol in basic medium
Sorba, Giovanni,Ermondi, Giuseppe,Fruttero, Roberta,Galli, Ubaldina,Gasco, Alberto
, p. 327 - 334 (2007/10/03)
The use of benzenesulfonyl substituted furoxans as flexible intermediates for the synthesis of new functionalized furoxans interesting for their potential biological properties is discussed. Reaction of benzenesulfonylphenylsulfonylfuroxan isomers 7a and 7b with ethanol and ethanethiol in basic medium affords the expected ethers and sulphides respectively. Reaction of bis(benzenesulfonyl)furoxan (1) with ethanol in basic medium gives 3-benzenesulfonyl-4-ethoxyfuroxan (2) or diethoxyfuroxan (3), according to the experimental procedure. In contrast the reaction of 1 with ethanethiol gives a mixture of substitution compounds and the 4-benzenesulfonyl-3-ethylthiofurazan (11). The structure of the compounds has been assigned by nmr spectroscopy and, in the case of 3-benzenesulfonyl-4-ethylthiofuroxan (9b), confirmed by X-ray analysis.
