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2-phenyl-cycloheptane-1,3-dione is an organic compound characterized by a cycloheptane ring with a phenyl group attached to the 2nd carbon and two carbonyl groups (C=O) at the 1st and 3rd positions. This molecule features a unique structure that combines the properties of both aromatic and cyclic ketones. The phenyl group provides aromatic stability and conjugation, while the cycloheptane ring offers a strained, seven-membered carbon backbone. The two carbonyl groups enhance the molecule's reactivity and polarity, making it a potential candidate for various chemical reactions and applications in the fields of pharmaceuticals, materials science, and organic synthesis.

6852-99-9

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6852-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6852-99-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6852-99:
(6*6)+(5*8)+(4*5)+(3*2)+(2*9)+(1*9)=129
129 % 10 = 9
So 6852-99-9 is a valid CAS Registry Number.

6852-99-9Relevant academic research and scientific papers

Highly chemo- and regioselective rearrangement of α,β-epoxy ketones to 1,3-dicarbonyl compounds in 5 mol dm-3 lithium perchlorate-diethyl ether medium

Sankararaman,Ncsakumar

, p. 3173 - 3175 (1999)

Epoxides from α,β-unsaturated ketones undergo highly chemo- and regioselective rearrangement to 1,3-dicarbonyl compounds in 5 mol dm-3 lithium perchlorate-diethyl ether medium by a 1,2-migration of the carbonyl group at ambient conditions. The Royal Society of Chemistry 1999.

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