cis-2-Heptene (CAS 6443-92-1)
See product citations (1)
QUICK LINKS
Cis-2-Heptene is a colorless liquid with a sweet odor. It belongs to the group of organic compounds called hydrocarbons, which are composed of carbon and hydrogen atoms. Specifically, it is classified as an alkene, characterized by a double bond between two carbon atoms. This unique chemical structure makes cis-2-Heptene a valuable building block in the synthesis of numerous other organic compounds. Due to its versatility, cis-2-Heptene finds applications in various scientific research endeavors. It serves as a substrate in biocatalysis studies and functions as a reagent in organic synthesis. Furthermore, cis-2-Heptene is employed as a model compound to investigate the impact of double bonds on the physical and chemical properties of molecules. Its miscibility with most organic solvents further enhances its utility. Moreover, cis-2-Heptene plays a role in the creation of diverse organic compounds, including polymers and dyes. This compound′s reactivity stems from its double bond, which can be broken and re-formed through addition, substitution, or elimination reactions when exposed to various reagents. This characteristic makes cis-2-Heptene a pivotal component in the synthesis process.
Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA
LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences
cis-2-Heptene (CAS 6443-92-1) References
- Analysis of alkenes by copper ion chemical ionization gas chromatography/mass spectrometry and gas chromatography/tandem mass spectrometry. | Fordham, PJ., et al. 1999. J Mass Spectrom. 34: 1007-17. PMID: 10510423
- Improved operational stability of peroxidases by coimmobilization with glucose oxidase. | van de Velde, F., et al. 2000. Biotechnol Bioeng. 69: 286-91. PMID: 10861408
- Olefin cis-dihydroxylation versus epoxidation by non-heme iron catalysts: two faces of an Fe(III)-OOH coin. | Chen, K., et al. 2002. J Am Chem Soc. 124: 3026-35. PMID: 11902894
- Adducts of phenoxathiin and thianthrene cation radicals with alkenes and cycloalkenes. | Shine, HJ., et al. 2003. J Org Chem. 68: 8910-7. PMID: 14604362
- A structural and functional model for dioxygenases with a 2-His-1-carboxylate triad. | Oldenburg, PD., et al. 2006. Angew Chem Int Ed Engl. 45: 7975-8. PMID: 17096444
- Addition of the phenoxathiin cation radical to alkenes and nonconjugated dienes. Formation of (E)- and (Z)-(10-phenoxathiiniumyl)alkenes and (E)- and (Z)-(10-phenoxathiiniumyl)dienes on basic alumina. | Zhao, BJ., et al. 2007. J Org Chem. 72: 6154-61. PMID: 17602534
- Iron-catalyzed olefin epoxidation in the presence of acetic acid: insights into the nature of the metal-based oxidant. | Mas-Ballesté, R. and Que, L. 2007. J Am Chem Soc. 129: 15964-72. PMID: 18052063
- Ligand topology tuning of iron-catalyzed hydrocarbon oxidations. | Costas, M. and Que, L. 2002. Angew Chem Int Ed Engl. 41: 2179-81. PMID: 19746637
- Inverse solvent effects in the heterogeneous and homogeneous epoxidation of cis-2-heptene with [2-percarboxyethyl]-functionalized silica and meta-chloroperbenzoic acid. | Mello, R., et al. 2014. Org Biomol Chem. 12: 3246-50. PMID: 24728375
- Identification and Quantitation of Volatile Organic Compounds in Poly(methyl methacrylate) Kitchen Utensils by Headspace Gas Chromatography/Mass Spectrometry. | Ohno, H., et al. 2014. J AOAC Int. 97: 1452-8. PMID: 25902999
- Oxidation of aliphatic olefins by toluene dioxygenase: enzyme rates and product identification. | Lange, CC. and Wackett, LP. 1997. J Bacteriol. 179: 3858-65. PMID: 9190800
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
cis-2-Heptene, 1 ml | sc-239561 | 1 ml | $133.00 |