3-Methyl-1,4-pentadiene (CAS 1115-08-8)
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3-Methyl-1,4-pentadiene is a chemical compound that functions as a reactive diene in various organic reactions. Its double bonds make it highly reactive, allowing it to participate in Diels-Alder reactions, which are important in the synthesis of complex organic molecules. In these reactions, 3-Methyl-1,4-pentadiene acts as a dienophile, reacting with a diene to form a cyclic product. 3-Methyl-1,4-pentadiene can undergo polymerization reactions, where the double bonds link together to form long chains, contributing to the production of various polymers. 3-Methyl-1,4-pentadiene can serve as a precursor in the synthesis of other organic compounds, contributing to the formation of diverse chemical products. Its reactivity and ability to participate in various chemical reactions make it a valuable building block in organic synthesis, contributing to the production of a wide range of molecular components.
3-Methyl-1,4-pentadiene (CAS 1115-08-8) References
- Radical cascade reaction with 1,4-dienes and 1,4-enynes using 2-(iodomethyl)cyclopropane-1,1-dicarboxylate as a homoallyl radical precursor: one-step synthesis of bicyclo[3.3.0]octane derivatives. | Kitagawa, O., et al. 2002. Org Lett. 4: 1011-3. PMID: 11893209
- Reactions of carbocations with unsaturated hydrocarbons: electrophilic alkylation or hydride abstraction? | Mayr, H., et al. 2002. J Am Chem Soc. 124: 4076-83. PMID: 11942846
- Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation between salicylaldehydes and 1,4-penta- or 1,5-hexadienes. | Imai, M., et al. 2004. J Org Chem. 69: 1144-50. PMID: 14961663
- Method optimization by solid-phase microextraction in combination with gas chromatography with mass spectrometry for analysis of beer volatile fraction. | Pinho, O., et al. 2006. J Chromatogr A. 1121: 145-53. PMID: 16687150
- Group additive values for the gas phase standard enthalpy of formation of hydrocarbons and hydrocarbon radicals. | Sabbe, MK., et al. 2005. J Phys Chem A. 109: 7466-80. PMID: 16834116
- Simple method for reliable predicting flash points of unsaturated hydrocarbons. | Keshavarz, MH. and Ghanbarzadeh, M. 2011. J Hazard Mater. 193: 335-41. PMID: 21820804
- Tandem palladium(0) and palladium(II)-catalyzed allylic alkylation through complementary redox cycles. | Trost, BM., et al. 2012. Angew Chem Int Ed Engl. 51: 11522-6. PMID: 23055351
- The Interplay between a Multifunctional Dehydratase Domain and a C-Methyltransferase Effects Olefin Shift in Ambruticin Biosynthesis. | Berkhan, G., et al. 2016. Angew Chem Int Ed Engl. 55: 13589-13592. PMID: 27670141
- Kinetic Properties Study of H Atom Abstraction by CH3Ȯ2 Radicals from Fuel Molecules with Different Functional Groups. | Guo, HT., et al. 2023. J Phys Chem A. 127: 1960-1974. PMID: 36802637
- Asymmetric radiation-induced inclusion polymerization of 3-methyl-1,4-pentadiene in deoxycholic acid | F Cataldo, O Ursini, G Angelini. 2010. Radiation Physics and Chemistry. 79: 57-63.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Methyl-1,4-pentadiene, 5 ml | sc-226132 | 5 ml | $214.00 |