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  2. Isoprenol - Wikipedia

    en.wikipedia.org/wiki/Isoprenol

    Isoprenol, also known as 3-methylbut-3-en-1-ol, is a hemiterpene alcohol. It is produced industrially as an intermediate to 3-methylbut-2-en-1-ol (prenol): global production in 2001 can be estimated as 6–13 thousand tons.

  3. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    Structure Type IUPAC name Boiling point (°C) [3] 1-pentanol or normal amyl alcohol primary Pentan-1-ol: 138.5 2-methyl-1-butanol or active amyl alcohol primary 2-Methylbutan-1-ol: 128.7 3-methyl-1-butanol or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or neopentyl alcohol primary 2,2 ...

  4. Butyne - Wikipedia

    en.wikipedia.org/wiki/Butyne

    Toggle the table of contents. Butyne. 9 languages. ... 1-Butyne (ethylacetylene) 2-Butyne (dimethylacetylene) See also. C 4 H 6; Butane (C 4 H 10)

  5. 1-Butyne - Wikipedia

    en.wikipedia.org/wiki/1-Butyne

    1-Butyne is an organic compound with the formula CH 3 CH 2 C≡CH. It is a terminal alkyne. The compound is a common terminal alkyne substrate in diverse studies of catalysis. It is a colorless combustible gas. [1] 1-Butyne participates in reactions typical for terminal alkynes, such as alkyne metathesis, [2] hydrogenation, condensation with ...

  6. 2-Methylbut-3-yn-2-ol - Wikipedia

    en.wikipedia.org/wiki/2-Methylbut-3-yn-2-ol

    The addition can be promoted with base [1] (Favorskii reaction) or with Lewis acid catalysts. [2] 2-Methylbut-3-yn-2-ol is produced on an industrial scale as a precursor to terpenes and terpenoids. 2-Methylbut-3-yn-2-ol is an intermediate in this industrial route to geraniol. [3] 2-Methylbut-3-yn-2-ol also is used as a monoprotected version of ...

  7. Isovaleraldehyde - Wikipedia

    en.wikipedia.org/wiki/Isovaleraldehyde

    Isovaleraldehyde organic compound, also known as 3-methylbutanal, with the formula (CH 3) 2 CHCH 2 CHO. It is an aldehyde, a colorless liquid at STP, [1] and found in low concentrations in many types of food. [2] Commercially it is used as a reagent for the production of pharmaceuticals, perfumes and pesticides. [3]

  8. -yne - Wikipedia

    en.wikipedia.org/wiki/-yne

    Locants are chosen to be as low as possible. While generally used as a suffix, "-yne" is also used as an infix to name substituent groups that are triply bound to the parent compound. This suffix arose as a collapsed form of the end of the word acetylene. The final "-e" disappears if it is followed by another suffix that starts with a vowel. [3]

  9. Butanol - Wikipedia

    en.wikipedia.org/wiki/Butanol

    Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).