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1-Phenyl-2-(4-phenyl-1,2,5-oxadiazol-3-yl)ethanone is a complex organic compound characterized by a unique molecular structure. It features a phenyl group (C6H5) attached to the first carbon atom of the ethane backbone, while the second carbon is connected to a 1,2,5-oxadiazole ring system. The oxadiazole ring is further substituted with a phenyl group at the 4-position. 1-phenyl-2-(4-phenyl-1,2,5-oxadiazol-3-yl)ethanone is known for its potential applications in various chemical and pharmaceutical industries, particularly as a building block for the synthesis of more complex molecules. Its chemical properties, such as reactivity and stability, make it a valuable intermediate in organic synthesis.

844-69-9

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844-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 844-69-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 844-69:
(5*8)+(4*4)+(3*4)+(2*6)+(1*9)=89
89 % 10 = 9
So 844-69-9 is a valid CAS Registry Number.

844-69-9Downstream Products

844-69-9Relevant academic research and scientific papers

Divergent Synthesis of Five-Membered Nitrogen Heterocycles via Cascade Reactions of 4-Arylfuroxans

Chaplygin, Daniil A.,Ananyev, Ivan V.,Fershtat, Leonid L.,Makhova, Nina N.

, p. 2667 - 2678 (2020/11/02)

A novel method for the synthesis of a diverse series of functionally substituted five-membered heterocyclic compounds via atom-economic, regio-, and diastereoselective one-pot reaction cascade was developed. This approach involves a ring opening in 4-aryl

Heterocyclic Rearrangements. Synthesis and Reactivity of Oximes of Some 3-Acylisoxazoles. A Reinvestigation

Vivona, Nicolo,Macaluso, Gabriella,Frenna, Vincenzo

, p. 483 - 486 (2007/10/02)

The oximation reaction of some 3-acylisoxazoles with hydroxylamine hydrochloride and the geometry of the product oximes were reinvestigated. 3-Benzoylisoxazoles gave mixtures of (E)- and (Z)-isomers, whereas 3-acetylisoxazoles gave (E)-isomers only.The base-induced rearrangement of 3-acylisoxazole oximes to 1,2,5-oxadiazoles (furazans) was reinvestigated and was shown to depend on the geometry of the oximes since, when treated with aqueous potassium hydroxide, only (Z)-oximes readily rearranged.On the basis of our findings, some discrepancies in the literature have been corrected.

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