83725-79-5 Usage
General Description
5-(2-nitrophenyl)-1,3,4-oxadiazol-2(3H)-one is a chemical compound used in various research and industrial applications. It is a nitro-substituted oxadiazole derivative that has potential antioxidant and antibacterial properties. The nitro group in the molecule is known to be a strong electron-withdrawing group, which makes this compound an interesting candidate in the development of new pharmaceuticals and agrochemicals. Additionally, its unique structural and electronic properties make it a valuable building block in the synthesis of more complex organic molecules. Overall, 5-(2-nitrophenyl)-1,3,4-oxadiazol-2(3H)-one is an important compound with various potential applications in the fields of medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 83725-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83725-79:
(7*8)+(6*3)+(5*7)+(4*2)+(3*5)+(2*7)+(1*9)=155
155 % 10 = 5
So 83725-79-5 is a valid CAS Registry Number.
83725-79-5Relevant articles and documents
Substituted phenyl derivatives, their preparation and use
-
, (2008/06/13)
The present invention discloses compounds having the formula wherein the substituents are defined in the application. The compounds are useful as chloride channel blockers.
Substituted phenyl derivatives, their preparation and use
-
, (2008/06/13)
A compound having the formula (I) or a pharmaceutically acceptable salt thereof where the variables are defined in the specification are useful in the treatment of sickle-cell anemia.
1,3,4-Oxadiazolin-2-ones from Carbo-t-butoxyhydrazones
Baumgarten, Henry E.,Hwang, Deng-Ruey,Rao, T. N.
, p. 945 - 949 (2007/10/02)
5-Substituted-1,3,4-oxadiazolin-2-ones 2 were synthesized by the oxidation of carbo-t-butoxyhydrazones 1 of aromatic aldehydes with lead tetraacetate or, preferably, iodosobenzene diacetate.In some instances 5-acetoxy-1,3,4-oxadiazoles 3 were obtained along with 2.The oxidation of carboethoxyhydrazones 4 gave 2-ethoxy-1,3,4-oxadiazoles 5.
