Molecular structure of Methylenecyclopentane, CAS Number: 1528-30-9
Methylenecyclopentane (CAS 1528-30-9)
CAS Number:
1528-30-9
Molecular Weight:
82.14
Molecular Formula:
C6H10
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Methylenecyclopentane (MCP) is a cyclic hydrocarbon molecule used as a starting material for the synthesis of other compounds. Also, it acts as an antioxidant by scavenging free radicals and reduces inflammation by inhibiting the production of pro-inflammatory molecules. In addition, it may act to reduce the levels of certain hormones, including cortisol and testosterone. Methylenecyclopentane has been studied for its potential use in the synthesis of polymers, the production of biofuels, and as a fuel additive.
Methylenecyclopentane (CAS 1528-30-9) References
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- Cobalt-catalyzed intramolecular Heck-type reaction of 6-halo-1-hexene derivatives. | Fujioka, T., et al. 2002. Org Lett. 4: 2257-9. PMID: 12074681
- Palladium(II) acetate mediated oxidative cyclization of omega-unsaturated alpha-cyano ketones. A facile methylenecyclopentane annulation process. | Kung, LR., et al. 2003. Chem Commun (Camb). 2490-1. PMID: 14587746
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- Development of an asymmetric trimethylenemethane cycloaddition reaction: application in the enantioselective synthesis of highly substituted carbocycles. | Trost, BM., et al. 2011. J Am Chem Soc. 133: 19483-97. PMID: 21936576
- Enantiospecific intramolecular Heck reactions of secondary benzylic ethers. | Harris, MR., et al. 2014. J Am Chem Soc. 136: 7825-8. PMID: 24852707
- Diastereoselective Synthesis of 6″-(Z)- and 6″-(E)-Fluoro Analogues of Anti-hepatitis B Virus Agent Entecavir and Its Evaluation of the Activity and Toxicity Profile of the Diastereomers. | Kumamoto, H., et al. 2016. J Org Chem. 81: 2827-36. PMID: 27009432
- Synthesis of functionalized cyclopentenes through allenic ketone-based multicomponent reactions. | Wang, Q., et al. 2018. Org Biomol Chem. 16: 8854-8858. PMID: 30411769
- NHC/Nickel(II)-Catalyzed [3+2] Cross-Dimerization of Unactivated Olefins and Methylenecyclopropanes. | Huang, JQ. and Ho, CY. 2020. Angew Chem Int Ed Engl. 59: 5288-5292. PMID: 31943646
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Methylenecyclopentane, 1 g | sc-257799 | 1 g | $124.00 |