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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. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    2-Methyl-2-butene (CAS 513-35-9) Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  4. 2-Methyl-2-butene - Wikipedia

    en.wikipedia.org/wiki/2-Methyl-2-butene

    2-Methyl-2-butene, 2m2b, 2-methylbut-2-ene, beta-isoamylene, or Trimmethylethylene is an alkene hydrocarbon with the molecular formula C 5 H 10. Used as a free radical scavenger in trichloromethane (chloroform) and dichloromethane (methylene chloride). It is also used to scavenge hypochlorous acid (HOCl) in the Pinnick oxidation.

  5. C5H10S - Wikipedia

    en.wikipedia.org/wiki/C5H10S

    Prenylthiol, also known as 3-methyl-2-butene-1-thiol Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  6. C6H12 - Wikipedia

    en.wikipedia.org/wiki/C6H12

    Download as PDF; Printable version; In other projects ... 3-Methyl-2-pentene; 4-Methyl-2-pentene; Dimethylbutenes. 2,3-Dimethyl-1-butene; 3,3-Dimethyl-1-butene;

  7. Allylic rearrangement - Wikipedia

    en.wikipedia.org/wiki/Allylic_rearrangement

    In the similar substitution of 1-chloro-3-methyl-2-butene, the secondary 2-methyl-3-buten-2-ol is produced in a yield of 85%, while that for the primary 3-methyl-2-buten-1-ol is 15%. Allylic shifts occur because the transition state is an allyl intermediate.

  8. Prenol - Wikipedia

    en.wikipedia.org/wiki/Prenol

    Prenol, or 3-methyl-2-buten-1-ol, is a natural alcohol. It is one of the most simple terpenoids. It is a clear colorless oil that is reasonably soluble in water and miscible with most common organic solvents. It has a fruity odor and is used occasionally in perfumery.

  9. Prilezhaev reaction - Wikipedia

    en.wikipedia.org/wiki/Prilezhaev_reaction

    For example, the relative rates of epoxidation increase upon methyl substitution of the alkene (the methyl groups increase the electron density of the double bond by hyperconjugation): ethylene (1, no methyl groups), propene (24, one methyl group), cis-2-butene (500, two methyl groups), 2-methyl-2-butene (6500, three methyl groups), 2,3 ...