1-Bromo-2-phenylpropane (CAS 1459-00-3)
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1-Bromo-2-phenylpropane is a compound that functions as an alkylating agent in research and development applications. Its mechanism of action involves the transfer of an alkyl group from the compound to a nucleophile, resulting in the formation of a covalent bond with the nucleophile. 1-Bromo-2-Phenylpropane is utilized to introduce alkyl groups into various organic compounds, allowing for the modification of molecular structures and the synthesis of new compounds. In experimental applications, 1-Bromo-2-phenylpropane serves as a reagent in organic synthesis reactions, facilitating the creation of diverse chemical compounds for research purposes. Its ability to alkylate nucleophiles may be a useful for the modification and functionalization of organic molecules, contributing to the advancement of chemical research and development.
1-Bromo-2-phenylpropane (CAS 1459-00-3) References
- Characterization of sirtuin inhibitors in nematodes expressing a muscular dystrophy protein reveals muscle cell and behavioral protection by specific sirtinol analogues. | Pasco, MY., et al. 2010. J Med Chem. 53: 1407-11. PMID: 20041717
- In vitro metabolism study of 2-isopropyl-9H-thioxanthen-9-one (2-ITX) in rat and human: evidence for the formation of an epoxide metabolite. | Aprile, S., et al. 2011. Xenobiotica. 41: 212-25. PMID: 21087117
- Identification of potent c-Src inhibitors strongly affecting the proliferation of human neuroblastoma cells. | Radi, M., et al. 2011. Bioorg Med Chem Lett. 21: 5928-33. PMID: 21856155
- Tunnelling control of chemical reactions--the organic chemist's perspective. | Ley, D., et al. 2012. Org Biomol Chem. 10: 3781-90. PMID: 22402570
- Discovery of salermide-related sirtuin inhibitors: binding mode studies and antiproliferative effects in cancer cells including cancer stem cells. | Rotili, D., et al. 2012. J Med Chem. 55: 10937-47. PMID: 23189967
- Studies on the ATP Binding Site of Fyn Kinase for the Identification of New Inhibitors and Their Evaluation as Potential Agents against Tauopathies and Tumors. | Tintori, C., et al. 2015. J Med Chem. 58: 4590-609. PMID: 25923950
- Discovery, synthesis, and structure-activity relations of 3,4-dihydro-1H-spiro(naphthalene-2,2'-piperidin)-1-ones as potassium-competitive acid blockers. | Imaeda, T., et al. 2017. Bioorg Med Chem. 25: 3719-3735. PMID: 28522264
- Deuterium and Tritium Isotope Effects in the Methoxide-Promoted Elimination Reaction of 2,2-Diphenylethyl Benzenesulfonate1 | A. V. Willi. 1966,. J. Phys. Chem. 70: 2705–2707.
- Effect of the Hydrogen Bond and the Solvent on Kinetics and the Mechanism of Intermolecular Proton Transitions | E. A. PSHENICHNOV, N. D. SOKOLOV. 1967. 1: 855-872.
- Photolysis of 1-bromo-2-phenylpropane. A photochemical phenyl migration involving free radicals | J. J. Dannenberg, K. Dill and H. P. Waits . 1971. J. Chem. Soc. D,. 1348-1349.
- Conformational interactions between a phenyl ring and a side-chain halide substituent: A 1H NMR and molecular mechanics study of some 2-aryl-1-halopropanes | Michael J. Cook, Trevor J. Howe. 1990. Spectrochimica Acta Part A: Molecular Spectroscopy. 46: 957-965.
- Chiral recognition of selenides and iodides by 1H NMR spectroscopy in the presence of a chiral dirhodium complex | Shahid Hameed, Roshan Ahmad, Helmut Duddeck. 1998. Heteroatom Chemistry. 9: 471-474.
- Flash vacuum pyrolysis over magnesium. Part 1. Pyrolysis of benzylic, other aryl/alkyl and aliphatic halides | R. Alan Aitken,*a Philip K. G. Hodgson,b John J. Morrisona and Adebayo O. Oyewalea . 2002. J. Chem. Soc., Perkin Trans. 1. 1: 402-415.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Bromo-2-phenylpropane, 1 g | sc-264752 | 1 g | $240.00 |