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1-p-Anisyl-4-phenyl-butan-2,4-dion is a complex organic compound with the molecular formula C18H16O4. It is characterized by a butan-2,4-dione core, which consists of a four-carbon chain with two carbonyl groups (C=O) at the second and fourth positions. The molecule features a p-anisyl group (a methoxy-substituted phenyl ring) attached to the first carbon and a phenyl group (a benzene ring) attached to the fourth carbon. This chemical structure endows the compound with unique properties, making it potentially useful in various applications, such as in the synthesis of pharmaceuticals or as a chemical intermediate. The specific reactivity and physical properties of 1-p-Anisyl-4-phenyl-butan-2,4-dion would depend on the context in which it is used and the reactions it undergoes.

95279-88-2

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95279-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95279-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,7 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95279-88:
(7*9)+(6*5)+(5*2)+(4*7)+(3*9)+(2*8)+(1*8)=182
182 % 10 = 2
So 95279-88-2 is a valid CAS Registry Number.

95279-88-2Downstream Products

95279-88-2Relevant academic research and scientific papers

A new synthesis and application of 1-aryl-2,4-diones

Kel'in, Alexander V.,Kozyrkov, Yurii Yu.

, p. 729 - 734 (1998)

Methyl ketones or ethyl acetate react with aromatic α-bromo ketones in the presence of two equivalents of tert-butoxy or diethylaminomagnesium bromide in benzene (toluene) under reflux to produce 1-aryl-2,4-diones. The conversion, apparently, occurs via aldol condensation and subsequent [1,2]- sigmatropic rearrangement of the intermediate 3-bromo-2-hydroxy ketones. A number of fused aromatic and heteroaromatic phenols have been prepared by cyclodehydration of 1-aryl-2,4-diones.

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