Cyclohexanemethylamine (CAS 3218-02-8)
QUICK LINKS
Cyclohexanemethylamine, also known as hexahydrobenzylcyanide (HHBC) or 1-cyano-2-methylcyclohexane, is an organic compound extensively utilized in scientific research. This colorless liquid exhibits a low melting point and emits a strong odor. Cyclohexanemethylamine finds widespread application in laboratory experiments, where it has been subjected to extensive study for its biochemical and physiological effects. Cyclohexanemethylamine plays a role in the investigation of enzymes, proteins, and other biomolecules. Additionally, it is employed in studying chemical reactions, particularly in the synthesis of other organic compounds. Although the precise mechanism of action for Cyclohexanemethylamine is not fully understood, it is postulated to interact with the active sites of enzymes, proteins, and other biomolecules. Furthermore, it is believed to engage with the cell membrane and other cellular components.
Cyclohexanemethylamine (CAS 3218-02-8) References
- Microgram-scale testing of reaction conditions in solution using nanoliter plugs in microfluidics with detection by MALDI-MS. | Hatakeyama, T., et al. 2006. J Am Chem Soc. 128: 2518-9. PMID: 16492019
- Novel NSAID 1-acyl-4-cycloalkyl/arylsemicarbazides and 1-acyl-5-benzyloxy/hydroxy carbamoylcarbazides as potential anticancer agents and antioxidants. | Perković, I., et al. 2012. Eur J Med Chem. 51: 227-38. PMID: 22405290
- Structure-activity relationship study of vitamin k derivatives yields highly potent neuroprotective agents. | Josey, BJ., et al. 2013. J Med Chem. 56: 1007-22. PMID: 23327468
- Revisiting the formation and tunable dissociation of a [2]pseudorotaxane formed by slippage approach. | Leung, KC., et al. 2015. Int J Mol Sci. 16: 8254-65. PMID: 25872145
- Regio- and Diastereoselective Synthesis of Highly Substituted, Oxygenated Piperidines from Tetrahydropyridines. | Chen, S., et al. 2015. J Org Chem. 80: 6660-8. PMID: 26098485
- Selection of a potential diagnostic biomarker for HIV infection from a random library of non-biological synthetic peptoid oligomers. | Gearhart, TL., et al. 2016. J Immunol Methods. 435: 85-9. PMID: 27182050
- Parthenolide Covalently Targets and Inhibits Focal Adhesion Kinase in Breast Cancer Cells. | Berdan, CA., et al. 2019. Cell Chem Biol. 26: 1027-1035.e22. PMID: 31080076
- Biochemical and microbiological evaluation of N-aryl urea derivatives against mycobacteria and mycobacterial hydrolases. | Vartak, A., et al. 2019. Medchemcomm. 10: 1197-1204. PMID: 31741730
- The novel amidocarbamate derivatives of ketoprofen: synthesis and biological activity. | Rajić, Z., et al. 2011. Med Chem Res. 20: 210-219. PMID: 32214761
- Discovery of a Small Molecule Inhibitor of Human Adenovirus Capable of Preventing Escape from the Endosome. | Xu, J., et al. 2021. Int J Mol Sci. 22: PMID: 33562748
- Betulonic Acid Derivatives Interfering with Human Coronavirus 229E Replication via the nsp15 Endoribonuclease. | Stevaert, A., et al. 2021. J Med Chem. 64: 5632-5644. PMID: 33877845
- Record high-Tc and large practical utilization level of electric polarization in metal-free molecular antiferroelectric solid solutions. | Xu, H., et al. 2022. Nat Commun. 13: 5329. PMID: 36088352
- Discovery of Novel Thiosemicarbazides Containing 1,3,5-Triazines Derivatives as Potential Synergists against Fluconazole-Resistant Candida albicans. | Xie, F., et al. 2022. Pharmaceutics. 14: PMID: 36365153
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Cyclohexanemethylamine, 5 g | sc-239614 | 5 g | $64.00 | |||
Cyclohexanemethylamine, 25 g | sc-239614A | 25 g | $166.00 |