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  2. 3-Pentanol - Wikipedia

    en.wikipedia.org/wiki/3-Pentanol

    Pentan-3-ol. Other names 3-Pentanol, diethyl carbinol ... 3-Pentanol is one of the eight isomers of amyl alcohol. It is found naturally and has a role as a pheromone ...

  3. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    Three of these alcohols, 2-methyl-1-butanol, 2-pentanol, and 3-methyl-2-butanol (methyl isopropyl carbinol), contain stereocenters, and are therefore chiral and optically active. The most important amyl alcohol is isoamyl alcohol , the chief one generated by fermentation in the production of alcoholic beverages and a constituent of fusel oil .

  4. 2-Pentanol - Wikipedia

    en.wikipedia.org/wiki/2-Pentanol

    2-Pentanol (IUPAC name: pentan-2-ol; also called sec-amyl alcohol) is an organic chemical compound.It is used as a solvent and an intermediate in the manufacturing of other chemicals. 2-Pentanol is a component of many mixtures of amyl alcohols sold industrially. 2-Pentanol is chiral and thus can be obtained as either of two stereoisomers designated as (R)-(−)-2-pentanol and (S)-(+)-2-pentanol.

  5. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    The optical center is the middle carbon of the pentane backbone, which is connected to one hydrogen atom, one methyl group, one ethyl group – C 2 H 5, and one isopropyl group – CH(CH 3) 2. The two enantiomers are denoted (3R)-2,3-dimethylpentane and (3S)-2,3-dimethylpentane (the other simplest chiral alkane is its structural isomer 3 ...

  6. Isoamyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Isoamyl_alcohol

    Isoamyl alcohol is a colorless liquid with the formula C 5 H 12 O, specifically (H 3 C–) 2 CH–CH 2 –CH 2 –OH. It is one of several isomers of amyl alcohol (pentanol). It is also known as isopentyl alcohol, isopentanol, or (in the IUPAC recommended nomenclature) 3-methyl-butan-1-ol.

  7. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    In naming simple alcohols, the name of the alkane chain loses the terminal e and adds the suffix -ol, e.g., as in "ethanol" from the alkane chain name "ethane". [19] When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3.

  8. Spiro compound - Wikipedia

    en.wikipedia.org/wiki/Spiro_compound

    [5]: 1138ff First, while nevertheless appearing to be twisted, they yet may have a chiral center making them analogous to any simple chiral compound, and second, while again appearing twisted, the specific location of substituents, as with alkylidenecycloalkanes, may make a spiro compound display central chirality (rather than axial chirality ...

  9. 3-Aminopentane - Wikipedia

    en.wikipedia.org/wiki/3-Aminopentane

    3-Aminopentane is the organic compound with the formula (CH 3 CH 2) 2 CHNH 2. It is a colorless liquid. It is a colorless liquid. It is of interest for producing soluble imides and imines without introducing a chiral center.