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1-Oxaspiro[4,5]decane-2,6-dione is a cyclic ketone with a unique spiro structure, consisting of a seven-membered ring (decane) and a five-membered ring (oxaspiro) connected at a single carbon atom. This organic compound has the molecular formula C8H12O3 and is characterized by two carbonyl groups (C=O) at positions 2 and 6 of the molecule. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its reactive ketone groups and rigid cyclic structure. The compound is also known for its potential applications in the development of novel materials and as a building block in organic synthesis.

4361-37-9

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4361-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4361-37-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4361-37:
(6*4)+(5*3)+(4*6)+(3*1)+(2*3)+(1*7)=79
79 % 10 = 9
So 4361-37-9 is a valid CAS Registry Number.

4361-37-9Downstream Products

4361-37-9Relevant academic research and scientific papers

Palladium(II)-catalyzed formation of γ-butyrolactones from 4-trimethylsilyl-3-alkyn-1-ols: Synthetic and mechanistic aspects

Compain, Philippe,Gore, Jacques,Vatele, Jean-Michel

, p. 10405 - 10416 (2007/10/03)

γ-butyrolactones are obtained in good yields from 4-trimethylsilyl-3-alkyn-1-ols via Wacker-type oxidation reaction. A mechanism is proposed for this transformation: it involves two successive trans-hydroxypalladations followed by a [PdXSiMe3] syn-elimination and explains why the presence of the silyl group is essential in such a process.

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