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2-phenylbicyclo[3.3.1]non-2-en-9-one is a complex organic compound characterized by a bicyclic structure with a phenyl group attached to the second carbon atom. This molecule features a unique arrangement of carbon atoms, forming a non-2-en-9-one functional group, which includes a carbonyl group (C=O) at the ninth position. The compound's structure can be visualized as a nine-membered ring with three carbon atoms forming a smaller ring fused to it, and a phenyl ring attached to the second carbon of the larger ring. This specific arrangement of atoms and functional groups gives 2-phenylbicyclo[3.3.1]non-2-en-9-one distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

5485-66-5

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5485-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5485-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,8 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5485-66:
(6*5)+(5*4)+(4*8)+(3*5)+(2*6)+(1*6)=115
115 % 10 = 5
So 5485-66-5 is a valid CAS Registry Number.

5485-66-5Upstream product

5485-66-5Relevant academic research and scientific papers

2-Substituted bicyclo[3.2.1]oct-2-en-8-ones by carbonylation of cycloheptadiene-derived iron carbonyl complexes bearing alkyl-alkyl subunits

Hirschfelder,Eilbracht

, p. 587 - 591 (1995)

Iron carbonyl complexes 7, generated by the reaction of cationic cycloheptadienyl complex 6 [L = P(OPh)3] with appropriate nucleophiles, can be converted into bicyclooctenones 9 and 10 via carbonylative decomplexation. Treatment of 7 with CO (2

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