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α-(2,4-Xylidin-1-yl)benzyl-phenylketon is a complex organic compound with the molecular formula C23H23NO. It is a derivative of benzophenone, featuring a benzyl group attached to the alpha carbon of the ketone. The xylidinyl group, which is a substituted aniline, is attached to the benzyl group, specifically at the 2,4-positions relative to the nitrogen atom. α-(2,4-Xylidin-1-yl)benzyl-phenylketon is characterized by its aromatic structure and the presence of a carbonyl group, which contributes to its chemical reactivity. It is typically synthesized through organic chemistry methods and may have applications in the fields of pharmaceuticals, materials science, or as an intermediate in the synthesis of other complex molecules. Due to its specific structure, it can participate in various chemical reactions, such as nucleophilic addition to the carbonyl group, and may exhibit unique physical and chemical properties.

38855-43-5

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38855-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38855-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,5 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38855-43:
(7*3)+(6*8)+(5*8)+(4*5)+(3*5)+(2*4)+(1*3)=155
155 % 10 = 5
So 38855-43-5 is a valid CAS Registry Number.

38855-43-5Downstream Products

38855-43-5Relevant academic research and scientific papers

THE SELECTIVE REDUCTIVE ACYLATION OF α-KETO IMINES

Alper, Howard,Amaratunga, Shiyamaline

, p. 3811 - 3812 (2007/10/02)

Reaction of α-keto imines with the in situ generated acetylcobalt tetracarbonyl occurs only at the carbon-nitrogen double bond to give β-keto amides.An unexpected by-product was formed in several instances.

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