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6-Allyl-2,4,6-trimethyl-2,4-cyclohexadien-1-one is a chemical compound with the molecular formula C??H??O. It is an organic compound belonging to the class of cyclohexadienones, which are cyclic compounds with alternating double and single bonds. This specific compound features a cyclohexadienone ring with three methyl groups (CH?) at positions 2, 4, and 6, and an allyl group (CH?=CH-CH?) attached to the 6th carbon. The allyl group provides a double bond and an additional carbon atom, contributing to the compound's reactivity and potential applications in organic synthesis. 6-allyl-2,4,6-trimethyl-2,4-cyclohexadien-1-one is known for its role as an intermediate in the synthesis of various fragrances and pharmaceuticals, and it is also used in the production of certain flavorings. Its structure and properties make it a versatile building block in the chemical industry.

4278-92-6

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4278-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4278-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4278-92:
(6*4)+(5*2)+(4*7)+(3*8)+(2*9)+(1*2)=106
106 % 10 = 6
So 4278-92-6 is a valid CAS Registry Number.

4278-92-6Relevant academic research and scientific papers

On the way to an oxidative Hosomi-Sakurai reaction

Sabot, Cyrille,Commare, Bruno,Duceppe, Marc-Alexandre,Nahi, Salima,Guérard, Kimiaka C.,Canesi, Sylvain

experimental part, p. 3226 - 3230 (2009/06/06)

An oxidative allylation process mediated by a hypervalent iodine reagent has been performed on polysubstituted phenols. This reaction, occurring in useful to good yields, leads to a rapid access to dienones containing a quaternary carbon center. Georg Thieme Verlag Stuttgart.

Electron transfer induced dissociations of 2- and 4-alkyl cyclohexadienones

McCarroll, Andrew J.,Crayston, Joe A.,Walton, John C.

, p. 4275 - 4280 (2007/10/03)

Several 2- and 4-alkylcyclohexadienones were prepared and shown to accept electrons to produce ketyl radical anions that dissociated rapidly at room temperature to release carbon-centered radicals and an aromatic phenoxide type anion. In the PET process with benzyl-substituted cyclohexadienones, initiated with triethylamine, the benzyl radicals dimerised or abstracted an H-atom from solvent. In electrochemical reductions, and in reductions with alkali metals in liquid ammonia, the benzyl radicals were further reduced to anions.

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