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2,2,4,4-tetramethyl-6-methylene-3-(1-methylethenyl)-cyclohexanone is a complex organic compound with the molecular formula C15H24O. It is a cyclic ketone with a unique structure, featuring a cyclohexanone ring that is substituted with four methyl groups (at positions 2, 2, 4, and 4), a methylene group (at position 6), and a 1-methylethylidene group (at position 3). 2,2,4,4-tetramethyl-6-methylene-3-(1-methylethenyl)-cyclohexanone is known for its potential applications in the synthesis of various chemicals and materials, such as fragrances, pharmaceuticals, and polymers. Due to its specific structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest in organic chemistry research.

81517-78-4

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81517-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81517-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,1 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81517-78:
(7*8)+(6*1)+(5*5)+(4*1)+(3*7)+(2*7)+(1*8)=134
134 % 10 = 4
So 81517-78-4 is a valid CAS Registry Number.

81517-78-4Relevant academic research and scientific papers

Homologues of Monocyclic Monoterpenes. Tetramethylated Derivatives of Carvone, Carveol, β-Terpineol, Sobrerol, and Related Compounds

Giguere, Raymond J.,Ilsemann, Godard von,Hoffmann, H. M. R.

, p. 4948 - 4954 (2007/10/02)

Epoxidation of tetramethyllimonene (1) gave monoepoxide 2t, which was opened regioselectively to endo and exo tetramethylated trans-carveols 3t and 5t, respectively.The alcohols were further oxidized to tetramethylcarvone (4) and its unstable exocyclic is

OXYGENATED LIMONENE ANALOGS. PREPARATION OF TETRAMETHYLATED CARVONE AND CARVEOLS VIA REGIOCONTROLLED OPENING OF TETRAMETHYLLIMONENE OXIDE.

Giguere, Raymond J.,Hoffmann, H. M. R.

, p. 5039 - 5042 (2007/10/02)

Regioselective opening of trans epoxide 2 gave endo and exo tetramethylated trans carveols 3t and 4t, respectively, which were oxidized to tetramethylcarvone (5) and its unstable exocyclic isomer 6; reduction of 5 with DIBAH gave tetramethylated cis carve

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