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Methyl Cyclopentenolone

Methyl Cyclopentenolone 112.13/C6H802/ white, cryst powder/ s—ale, prop glycol 1 g in 5 mL... [Pg.592]

Cyciosai. See Cyclamen aldehyde Cyclotene. See 3-Methyl-2-cyclopenten-2-ol-1-one Methyl cyclopentenolone Cycioteric BET-L31. See Lauryl betaine Cycioteric BET-OB50. See Oleyl betaine Cycioteric CAPA. See Cocaminopropionic acid Cycioteric SUP. See Sod i u m lauriminodipropionate Cyclotetradecanone... [Pg.1137]

MCP. See Calcium phosphate monobasic monohydrate Methyl cyclopentenolone... [Pg.2505]

Synonyms 2-Cyclopenten-1-one, 2-hydroxy-3-methyl- Cyclotene 2-Hydroxy-3-methylcyclopent-2-enone 2-Hydroxy-3-methyl-2-cyclopenten-1-one Hydroxy-3-methylcyclopent-2-en-1 -one Kentonarome Maple lactone 3-Methylcyclopentan-1,2-dione 3-Methylcyclopentane-1,2-dione 3-Methyl-2-cycl opentene-2-ol-one Methyl cyclopentenolone Methyl-2-cyclopenten-2-ol-1-one Empirical C6Hs02... [Pg.2612]

Methyl-2-cyclohexen-1 -one Methyl cyclopentenolone Methyidihydrojasmonate Methyl disulfide Methyl ester of rosin, partially hydrogenated... [Pg.5285]

Methylcinnamonitrile y-Methylcinnamyl acetate Methylcinnamyl alcohol 3-(4-Methylcyclohex-3-enyl) but-3-enyl acetate Methyl cyclopentenolone... [Pg.5323]

Methyl cyclopentenolone 1-Methyl-1-methoxycyclododecane Methyl a-naphthyl ketone Methyl 2-nonynoate Methyl 2-octynoate... [Pg.5329]

Cyclopentenolones with a planar vicinal enol-oxo configuration are known to be powerful aroma active substances with distinct caramel notes. By methylation of the enolic function, this flavour impression is changed drastically to a sweet, mildew, and mouldy odour in the case of 2,5-dimethyl-4-methoxy-3-[2H]-furanone (2). This so-called mesifurane as well as pineapple ketone (1) were stereodifferentiated with modified cyclodextrin [103], Although (1) and (2) can be stereoanalyzed without any racemization, both compounds were detected in strawberries, pineapples, grapes and wines as racemates (Fig. 6.43). [Pg.688]

The compounds formed in fructose syrup of pH 8-10 heated for 3h are listed in Table 4.12. The cyclopentenolones are typical caramel-like aroma substances. The formation of 2-hydroxy-3-methyl-2-cyclopenten-l-one as an example is shown in Formula 4.46. The compound l,3,5-trideoxy-2,5-hexulose is formed as an intermediate via the aldol condensation... [Pg.268]

See other pages where Methyl Cyclopentenolone is mentioned: [Pg.593]    [Pg.640]    [Pg.169]    [Pg.2127]    [Pg.6157]    [Pg.6797]    [Pg.7042]    [Pg.593]    [Pg.640]    [Pg.169]    [Pg.2127]    [Pg.6157]    [Pg.6797]    [Pg.7042]    [Pg.275]    [Pg.275]    [Pg.367]    [Pg.367]    [Pg.210]   
See also in sourсe #XX -- [ Pg.592 , Pg.593 ]

See also in sourсe #XX -- [ Pg.169 ]



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Cyclopentenolones

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