3-Bromo-1-phenyl-1-propene (CAS 4392-24-9)
QUICK LINKS
3-Bromo-1-phenyl-1-propene, a versatile organic compound, plays a significant role in scientific research due to its remarkable alkylating properties. Scientists employ it to create a variety of organic compounds, including esters, amides, and amines. Moreover, 3-Bromo-1-phenyl-1-propene finds application in modifying the structures of proteins and peptides. The mechanism of 3-Bromo-1-phenyl-1-propene′s action hinges on the formation of a covalent bond between this compound and the target molecule. This interaction leads to the generation of a new, more stable molecule, effectively altering the chemical structure of the original one. Such capabilities make 3-Bromo-1-phenyl-1-propene an invaluable tool in the world of scientific exploration and innovation.
3-Bromo-1-phenyl-1-propene (CAS 4392-24-9) References
- Iminosugars: potential inhibitors of liver glycogen phosphorylase. | Jakobsen, P., et al. 2001. Bioorg Med Chem. 9: 733-44. PMID: 11310609
- Antioxidant activity of unexplored indole derivatives: synthesis and screening. | Estevão, MS., et al. 2010. Eur J Med Chem. 45: 4869-78. PMID: 20727623
- Substituted E-3-(3-indolylmethylene)1,3-dihydroindol-2-ones with antiproliferative activity. Study of the effects on HL-60 leukemia cells. | Leoni, A., et al. 2014. Eur J Med Chem. 79: 382-90. PMID: 24747749
- (4-(Bis(4-fluorophenyl)methyl)piperazin-1-yl)(cyclohexyl)methanone hydrochloride (LDK1229): a new cannabinoid CB1 receptor inverse agonist from the class of benzhydryl piperazine analogs. | Mahmoud, MM., et al. 2015. Mol Pharmacol. 87: 197-206. PMID: 25411367
- Stereoselective nucleophilic addition of PhSCF2 SiMe3 to chiral cyclic nitrones: asymmetric synthesis of gem-difluoromethylenated polyhydroxypyrrolizidines and -indolizidines. | Korvorapun, K., et al. 2015. Chem Asian J. 10: 948-68. PMID: 25418141
- Asymmetric Synthesis of 2-Substituted Azetidin-3-ones via Metalated SAMP/RAMP Hydrazones. | Pancholi, AK., et al. 2016. J Org Chem. 81: 7984-92. PMID: 27447363
- α-Trifluoromethylated tertiary homoallylic amines: diastereoselective synthesis and conversion into β-aminoesters, γ- and δ-aminoalcohols, azetidines and pyrrolidines. | Grellepois, F., et al. 2017. Org Biomol Chem. 15: 9696-9709. PMID: 29125173
- The marine natural product mimic MPM-1 is cytolytic and induces DAMP release from human cancer cell lines. | von Hofsten, S., et al. 2022. Sci Rep. 12: 15586. PMID: 36114339
- Unveiling a New Selenocyanate as a Multitarget Candidate with Anticancer, Antileishmanial and Antibacterial Potential. | Ramos-Inza, S., et al. 2022. Molecules. 27: PMID: 36364304
- Synthesis of chiral malonates by α-alkylation of 2,2-diphenylethyl tert-butyl malonates via enantioselective phase-transfer catalysis. | Guo, Z., et al. 2023. Front Chem. 11: 1205661. PMID: 37361022
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Bromo-1-phenyl-1-propene, 5 g | sc-238496 | 5 g | $46.00 | |||
3-Bromo-1-phenyl-1-propene, 25 g | sc-238496A | 25 g | $117.00 | |||
3-Bromo-1-phenyl-1-propene, 100 g | sc-238496B | 100 g | $357.00 |