1,2-Acenaphthylenedione, 3,8-dimethyl- is an organic compound characterized by its unique structure, which includes a fused ring system typical of acenaphthylene derivatives. This compound features two carbonyl groups (ketones) at the 1 and 2 positions of the acenaphthylene framework, contributing to its reactivity and potential applications in organic synthesis. The presence of two methyl groups at the 3 and 8 positions introduces additional steric and electronic effects, which can influence its chemical behavior and interactions. Typically, such compounds exhibit properties like moderate solubility in organic solvents and may participate in various chemical reactions, including electrophilic aromatic substitution and oxidation. The compound's specific applications can vary, but it may be explored in fields such as materials science, pharmaceuticals, or as intermediates in organic synthesis. Safety data and handling precautions should be consulted, as with any chemical substance, to ensure proper laboratory practices.

1,2-Acenaphthylenedione, 3,8-dimethyl-

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3,8-Dimethylacenaphthenequinone is a molecule that has undergone chemical transformation in the form of cyclophane. It is a corannulene moiety that can undergo photochemical reactions and thermally induced reactions. 3,8-Dimethylacenaphthenequinone has been shown to have an encapsulation form with thermal energy which is used in research and environment.

CAS 146885-81-6: 1,2-Acenaphthylenedione, 3,8-dimethyl-

3,8-Dimethylacenaphthenequinone

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3,8-Dimethylacenaphthenequinone

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3,8-Dimethylacenaphthenequinone

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