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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.
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.
C 4 H 8 Molar mass: 56.106 g/mol Density: 0.641 g/ml (cis, 3.7 °C) [1] 0.626 g/ml (trans, 0.9 °C) [2] Melting point: −138.9 °C (−218.0 °F; 134.2 K) (cis) [1] −105.5 °C (trans) [2] Boiling point: 0.8 to 3.7 °C (33.4 to 38.7 °F; 273.9 to 276.8 K) (Z = 3.7 °C) [1] (E = 0.8 °C) [2]
The following other wikis use this file: Usage on ar.wikipedia.org 2-ميثيل-2-بوتين; Usage on de.wikipedia.org Olefine; 2-Methyl-2-buten
Methyl vinyl ketone (MVK, IUPAC name: butenone) is the organic compound with the formula CH 3 C(O)CH=CH 2. It is a reactive compound classified as an enone, in fact the simplest example thereof. It is a colorless, flammable, highly toxic liquid with a pungent odor. It is soluble in water and polar organic solvents.
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-Dimethylpropan-1-ol: 113.1 2-pentanol or sec-amyl alcohol or methyl (n) propyl carbinol secondary Pentan-2-ol: 118.8 3-methyl-2-butanol or sec-isoamyl alcohol or methyl ...
2-Methyl-1-butanol (IUPAC name, also called active amyl alcohol) is an organic compound with the formula CH 3 CH 2 CH(CH 3)CH 2 OH. It is one of several isomers of amyl alcohol.This colorless liquid occurs naturally in trace amounts and has attracted some attention as a potential biofuel, exploiting its hydrophobic (gasoline-like) and branched structure.
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 ...