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  2. Tetramethylethylene - Wikipedia

    en.wikipedia.org/wiki/Tetramethylethylene

    Tetramethylethylene is a hydrocarbon with the formula Me 2 C=CMe 2 (Me = methyl). ... It can be prepared by base-catalyzed isomerization of 2,3-dimethyl-1-butene. [2]

  3. 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).

  4. 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 .

  5. Prenylthiol - Wikipedia

    en.wikipedia.org/wiki/Prenylthiol

    Prenylthiol or 3-methyl-2-butene-1-thiol is a chemical compound. It is one of a group of chemicals that give cannabis its characteristic "skunk-like" aroma. It is also present in lightstruck or "skunky" beer. [2] [3]

  6. 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.

  7. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    For example, of the isomers of butene, the two methyl groups of (Z)-but-2-ene (a.k.a. cis-2-butene) appear on the same side of the double bond, and in (E)-but-2-ene (a.k.a. trans-2-butene) the methyl groups appear on opposite sides. These two isomers of butene have distinct properties.

  8. Isobutylene - Wikipedia

    en.wikipedia.org/wiki/Isobutylene

    Isobutylene (or 2-methylpropene) is a hydrocarbon with the chemical formula (CH 3) 2 C=CH 2. It is a four-carbon branched alkene (olefin), one of the four isomers of butylene . It is a colorless flammable gas, and is of considerable industrial value.

  9. Dimethylbutadiene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutadiene

    Dimethylbutadiene readily undergoes Diels-Alder reactions and reacts faster than 1,3-butadiene. Its effectiveness in this reaction is attributed to the stabilization of the cis-conformation owing to the influence of the methyl groups on the C2 and C3 positions. Diels-Alder reaction using 2,3-dimethyl-1,3-butadiene and N-ethylmaleimide