CAS 16523-32-3
:2,5-Bis(acetyloxy)-2,5-cyclohexadiene-1,4-dione
Description:
2,5-Bis(acetyloxy)-2,5-cyclohexadiene-1,4-dione, with the CAS number 16523-32-3, is an organic compound characterized by its unique structure, which includes a cyclohexadiene core with two acetyloxy substituents. This compound typically exhibits a yellow to orange color, indicative of its conjugated system, which can absorb visible light. It is known for its reactivity, particularly in electrophilic aromatic substitution reactions due to the presence of the dione functional groups. The acetyloxy groups enhance its solubility in organic solvents and may influence its stability and reactivity. Additionally, this compound can participate in various chemical transformations, making it of interest in synthetic organic chemistry. Its potential applications may include use as an intermediate in the synthesis of more complex organic molecules or as a dye due to its chromophoric properties. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly.
Formula:C10H8O6
InChI:InChI=1S/C10H8O6/c1-5(11)15-9-3-8(14)10(4-7(9)13)16-6(2)12/h3-4H,1-2H3
InChI key:InChIKey=NAWAHSSRMQMAFB-UHFFFAOYSA-N
SMILES:O(C(C)=O)C=1C(=O)C=C(OC(C)=O)C(=O)C1
Synonyms:- 2,5-Bis(acetyloxy)-2,5-cyclohexadiene-1,4-dione
- 2,5-Diacetoxy-p-benzoquinone
- 2,5-Cyclohexadiene-1,4-dione, 2,5-bis(acetyloxy)-
- 2,5-Diacetoxy-1,4-benzoquinone
- p-Benzoquinone, 2,5-dihydroxy-, diacetate
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