Methylcyclopentane (CAS 96-37-7)
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Methylcyclopentane is a compound that is of interest in organic chemistry and industrial applications. The research surrounding this compound often involves its use as a non-polar solvent due to its ability to dissolve hydrophobic substances. In synthetic chemistry, methylcyclopentane serves as a starting material for the synthesis of more complex organic molecules and is studied for its reactivity in various chemical reactions, including hydrogenation and ring-opening processes. Additionally, the compound′s role in the study of hydrocarbon behavior under extreme conditions, such as high pressures and temperatures, is significant for understanding and improving industrial processes like oil refining. Research on methylcyclopentane also contributes to the development of new synthetic strategies for cyclic compounds, which are prevalent in many natural products and industrial materials.
Methylcyclopentane (CAS 96-37-7) References
- Effects of gasoline components on MTBE and TBA cometabolism by Mycobacterium austroafricanum JOB5. | House, AJ. and Hyman, MR. 2010. Biodegradation. 21: 525-41. PMID: 20012341
- Synthesis and antiviral evaluation of C5-substituted-(1,3-diyne)-2'-deoxyuridines. | Sari, O., et al. 2012. Eur J Med Chem. 53: 220-8. PMID: 22578783
- Evaluation of subchronic inhalation toxicity of methylcyclopentane in rats. | Yang, YS., et al. 2014. Food Chem Toxicol. 63: 186-94. PMID: 24239891
- Carbon-carbon bond cleavage and rearrangement of benzene by a trinuclear titanium hydride. | Hu, S., et al. 2014. Nature. 512: 413-5. PMID: 25164752
- Effect of acidic properties of mesoporous zeolites supporting pt nanoparticles on hydrogenative conversion of methylcyclopentane. | Na, K., et al. 2014. J Am Chem Soc. 136: 17207-12. PMID: 25398051
- Anaerobic alkane biodegradation by cultures enriched from oil sands tailings ponds involves multiple species capable of fumarate addition. | Tan, B., et al. 2015. FEMS Microbiol Ecol. 91: PMID: 25873461
- Development and validation of a fast static headspace GC method for determination of residual solvents in permethrin. | Tian, J. and Rustum, A. 2016. J Pharm Biomed Anal. 128: 408-415. PMID: 27344630
- Insights into the Mechanism of n-Hexane Reforming over a Single-Site Platinum Catalyst. | Zhang, S., et al. 2020. J Am Chem Soc. 142: 16533-16537. PMID: 32926771
- The effect of introducing Ga on the ZSM-5-catalyzed methanol to aromatics reaction: taking methylcyclopentane to benzene as an example. | Zhang, D., et al. 2021. Phys Chem Chem Phys. 23: 10988-11003. PMID: 33929467
- Optimization of Residual Hexane in Edible Oils Analysis Using Static Headspace Gas Chromatography. | Samsuri, AH., et al. 2021. Int J Anal Chem. 2021: 1941336. PMID: 34745265
- From laboratory to industrial storage - Translating volatile organic compounds into markers for assessing garlic storage quality. | Ludlow, RA., et al. 2022. Postharvest Biol Technol. 191: 111976. PMID: 36061628
- Phytochemicals and antioxidant activity of alcoholic/hydroalcoholic extract of Trifolium pratense. | Akbaribazm, M., et al. 2020. Chin Herb Med. 12: 326-335. PMID: 36119012
- Shear-activated chemisorption and association of cyclic organic molecules. | Bhuiyan, FH., et al. 2023. Faraday Discuss. 241: 194-205. PMID: 36134558
- A comparative study on the toxicity of n-hexane and its isomers on the peripheral nerve. | Ono, Y., et al. 1981. Int Arch Occup Environ Health. 48: 289-94. PMID: 7251182
- Cytogenetic studies on commercial hexane solvent. | Daughtrey, WC., et al. 1994. J Appl Toxicol. 14: 161-5. PMID: 8083476
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Methylcyclopentane, 5 ml | sc-250392 | 5 ml | $37.00 | |||
Methylcyclopentane, 100 ml | sc-250392A | 100 ml | $62.00 |