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α-Benzoylisobutyraldehyde dioxime is a chemical compound with the molecular formula C11H13NO3. It is derived from α-benzoylisobutyraldehyde, a ketone, by reacting it with hydroxylamine to form the corresponding dioxime. α-benzoylisobutyraldehyde dioxime is an important intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It is characterized by its ability to form a cyclic structure due to the dioxime group, which can participate in various chemical reactions, such as oxidation, reduction, and condensation. The compound is typically synthesized in a two-step process: first, the formation of the aldehyde from the corresponding ketone, followed by the reaction with hydroxylamine to form the dioxime. Its structure and reactivity make it a valuable building block in the synthesis of complex organic molecules.

99390-62-2

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99390-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99390-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,9 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99390-62:
(7*9)+(6*9)+(5*3)+(4*9)+(3*0)+(2*6)+(1*2)=182
182 % 10 = 2
So 99390-62-2 is a valid CAS Registry Number.

99390-62-2Upstream product

99390-62-2Relevant academic research and scientific papers

Oxidative cyclization of some 1,3-Dioximes with Lead Tetraacetate

Stephanidou-Stephanatou, J.

, p. 293 - 295 (2007/10/02)

Oxidation of 1,3-dioximes 1 with lead tetraacetate gives di-N-oxides of pyrazolines 4 or pyrazoles 5 or N-oxides of oxadiazines 7 as the main reaction products.The reaction mechanism is discussed.

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