| Identification | Back Directory | [Name]
2-methylbutene | [CAS]
26760-64-5 | [Synonyms]
2-methyl-buten
2-METHYL-2-BUTENE (MIXTURE OF ISOMERS) F | [EINECS(EC#)]
247-975-0 | [Molecular Formula]
C5H10 | [MOL File]
26760-64-5.mol | [Molecular Weight]
70.13 |
| Chemical Properties | Back Directory | [Melting point ]
-134°C | [Boiling point ]
38-40 °C | [density ]
0.662[at 20℃] | [vapor pressure ]
513 hPa ( 20 °C) | [storage temp. ]
Store at +2°C to +8°C. | [form ]
liquid | [explosive limit]
1-9% (v/v) | [Water Solubility ]
193mg/L at 25℃ | [Cosmetics Ingredients Functions]
SOLVENT | [InChI]
1S/C5H10/c1-4-5(2)3/h2,4H2,1,3H3 | [InChIKey]
MHNNAWXXUZQSNM-UHFFFAOYSA-N | [SMILES]
C(C)C(=C)C | [EPA Substance Registry System]
2-Methylbutene (26760-64-5) |
| Hazard Information | Back Directory | [Uses]
- Palladium-Catalyzed Pentenylation of Indoles: A study demonstrated the use of 2-Methyl-2-butene in palladium-catalyzed intermolecular dehydrogenative pentenylation of indoles, offering a novel pathway in synthetic chemistry for creating complex molecules (Zhang et al., 2024).
- Asynchronous Concerted Mechanism: Research explored an asynchronous concerted mechanism in Lewis acid-mediated carbonyl-olefin [2+2] cycloaddition involving 2-Methyl-2-butene, providing insights into reaction dynamics and stereochemical outcomes in organic synthesis (Li et al., 2023).
| [Definition]
ChEBI: 2-methylbut-1-ene is an alkene that is but-1-ene carrying a methyl substituent at position 2. |
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Sigma-Aldrich
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https://www.sigmaaldrich.cn |
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