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2-Oxetanone, 4-ethylidene-3-methyl, also known as 3-Methyl-4-ethylidene-2-oxetanone, is an organic compound with the chemical formula C6H8O2. It is a cyclic ketone with a four-membered ring structure, featuring a carbonyl group (C=O) and a double bond between the third and fourth carbon atoms. The compound has a molecular weight of 112.13 g/mol and is characterized by its unique structure, which includes a methyl group (CH3) attached to the third carbon and an ethylidene group (CH2=CH-) on the fourth carbon. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is essential to handle 2-Oxetanone, 4-ethylidene-3-methyl with care, following proper safety protocols to minimize potential hazards.

5659-14-3

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5659-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5659-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5659-14:
(6*5)+(5*6)+(4*5)+(3*9)+(2*1)+(1*4)=113
113 % 10 = 3
So 5659-14-3 is a valid CAS Registry Number.

5659-14-3Upstream product

5659-14-3Relevant academic research and scientific papers

Mechanistic studies of the phosphine-catalyzed homodimerization of ketoketenes

Wei, Pei-Hsun,Ibrahim, Ahmad A.,Mondal, Mukulesh,Nalla, Divya,Harzmann, Gero D.,Tedeschi, Frank A.,Wheeler, Kraig A.,Kerrigan, Nessan J.

, p. 6690 - 6694 (2010)

The mechanism of PBu3-catalyzed homodimerization of ketoketenes has been explored and compared with that of the previously reported trialkylphosphite-mediated reactions. NMR studies of the PBu3- catalyzed reaction implicated the involvement of tetravalent phosphonium intermediates. Phosphonium intermediates in the catalytic cycle were trapped through reaction with trimethylsilyl chloride and 4-chlorobenzaldehyde, and the resulting products were characterized. A method for the stoichiometric generation of phosphonium enolates was developed as a result of these studies. No evidence was obtained for the involvement of pentacovalent phosphorane intermediates in trialkylphosphine-catalyzed ketoketene homodimerization reactions, in contrast with the mechanism of the trialkylphosphite-mediated homodimerization of dimethylketene. An X-ray crystal structure analysis of methylphenylketene dimer showed that it possesses Z-geometry about the exocyclic olefin.

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