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3-(4-Nitrophenyl)-5-phenyl-1,4,2-dioxazole is a complex organic compound characterized by a 1,4,2-dioxazole ring system, which is a five-membered heterocyclic ring containing two oxygen atoms and one nitrogen atom. The molecule features a 4-nitrophenyl group attached to the 3-position of the dioxazole ring and a phenyl group at the 5-position. 3-(4-Nitrophenyl)-5-phenyl-1,4,2-dioxazole is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique chemical structure and properties. The presence of the nitro group provides it with reactivity and the ability to participate in various chemical reactions, while the phenyl groups contribute to its stability and potential for further functionalization.

2289-99-8

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2289-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2289-99-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2289-99:
(6*2)+(5*2)+(4*8)+(3*9)+(2*9)+(1*9)=108
108 % 10 = 8
So 2289-99-8 is a valid CAS Registry Number.

2289-99-8Downstream Products

2289-99-8Relevant academic research and scientific papers

The Photochemistry of α-Nitrostilbenes and Related Compounds. A Study of Double Bond Cleavage Following Intramolecular Cyclization and Nitro-Nitrite Rearrangement

Grant, Richard D.,Pinhey, John T.,Rizzardo, Ezio

, p. 1217 - 1229 (2007/10/02)

A detailed study of the photochemistry of a number of α-nitrostilbenes is reported.The previously described intramolecular cyclization of (1) which resulted in cleavage of the double bond was not found to occur to any extent in the other compounds examined.The majority of the compounds were found to yield significant amounts of aldehydes and nitriles, which result from a new fragmentation pathway arising from initial photochemical nitro-nitrite isomerization.

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