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1-Propene-1,3-dione, 3-phenyl-2-[phenyl(phenylimino)methyl]-, also known as 3-phenyl-2-[phenyl(phenylimino)methyl]propane-1,3-dione, is a complex organic compound with the molecular formula C20H15NO2. 1-Propene-1,3-dione, 3-phenyl-2-[phenyl(phenylimino)methyl]- is characterized by a 1,3-dione functional group, which consists of two carbonyl groups (C=O) separated by a single carbon atom. The molecule features a phenyl group (C6H5) attached to the 3-position of the propane-1,3-dione backbone, and a phenylimino group (C6H5N=) connected to the 2-position through a phenylmethyl (C6H5CH2) linker. This specific arrangement of functional groups and aromatic rings contributes to the compound's unique chemical properties and potential applications in various fields, such as pharmaceuticals, materials science, and organic synthesis.

90368-08-4

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90368-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90368-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,6 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90368-08:
(7*9)+(6*0)+(5*3)+(4*6)+(3*8)+(2*0)+(1*8)=134
134 % 10 = 4
So 90368-08-4 is a valid CAS Registry Number.

90368-08-4Downstream Products

90368-08-4Relevant academic research and scientific papers

Reactive Nitrogenous Molecules from Meldrum's Acid Derivatives, Pyrrole-2,3-diones, and Isoxazolones

Briehl, Horst,Lukosch, Adelheid,Wentrup, Curt

, p. 2772 - 2779 (2007/10/02)

Flash vacuum pyrolysis of 5-(aminomethylidene)-2,2-dimethyl-1,3-dioxane-4,6-diones (Meldrum's acid derivatives) 12 gives 4-hydroxyquinolines/4-quinolones 15 or 3-enaminoacroleins 22 in good to excellent yields.Intermediate (aminomethylene)ketenes and imidoylketenes are directly observed and their transformation into product 22 monitored by low-temperature IR spectroscopy.Imidoylketenes are also formed and observed upon thermal CO extrusion from pyrrole-2,3-diones 16.Isocyanoamines and fulminates are generated by pyrolysis of hydrazono- or oximino-Meldrum's acid derivatives 32 and 39, monitored by IR spectroscopy, and found to rearrange to cyanamides and cyanates, depending on substituents.The thermal reactions of isoxazol-5(4H)-ones and Meldrum's acid derivatives are compared and discussed.

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