1-Acetylindole (CAS 576-15-8)
QUICK LINKS
1-Acetylindole is a chemical compound that functions as a precursor in the synthesis of various organic compounds. It acts as a key intermediate in the production of agrochemicals and other fine chemicals. Its mode of action involves participating in diverse chemical reactions, including condensation, cyclization, and substitution reactions, to yield complex molecular structures. 1-Acetylindole plays a role in the development of novel materials and compounds with potential industrial applications. Its functional role lies in its ability to undergo specific chemical transformations, leading to the creation of diverse chemical entities with unique properties. 1-Acetylindole serves as a versatile building block for the synthesis of a wide range of chemical compounds, contributing to the advancement of chemical research and development.
1-Acetylindole (CAS 576-15-8) References
- An enantioselective total synthesis of (+)-geissoschizine. | Martin, SF., et al. 1999. Org Lett. 1: 79-81. PMID: 10822538
- Direct palladium-catalyzed C-2 and C-3 arylation of indoles: a mechanistic rationale for regioselectivity. | Lane, BS., et al. 2005. J Am Chem Soc. 127: 8050-7. PMID: 15926829
- Light-induced oxidation of tryptophan and histidine. Reactivity of aromatic N-heterocycles toward triplet-excited flavins. | Huvaere, K. and Skibsted, LH. 2009. J Am Chem Soc. 131: 8049-60. PMID: 19459626
- Highly regioselective C-N bond formation through C-H azolation of indoles promoted by iodine in aqueous media. | Wu, WB. and Huang, JM. 2012. Org Lett. 14: 5832-5. PMID: 23163878
- The NSAIDs indomethacin and diflunisal as scavengers of photogenerated reactive oxygen species. | Purpora, R., et al. 2013. Photochem Photobiol. 89: 1463-70. PMID: 23789718
- Spectroscopic (FT-IR, FT-Raman, and UV-visible) and quantum chemical studies on molecular geometry, Frontier molecular orbitals, NBO, NLO and thermodynamic properties of 1-acetylindole. | Shukla, VK., et al. 2014. Spectrochim Acta A Mol Biomol Spectrosc. 133: 626-38. PMID: 24996206
- Recent Advances on the C2-Functionalization of Indole via Umpolung. | Deka, B., et al. 2020. Top Curr Chem (Cham). 378: 22. PMID: 32030596
- Multi-faceted reactivity of N-fluorobenzenesulfonimide (NFSI) under mechanochemical conditions: fluorination, fluorodemethylation, sulfonylation, and amidation reactions. | Hernández, JG., et al. 2022. Beilstein J Org Chem. 18: 182-189. PMID: 35233257
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Acetylindole, 1 g | sc-255790 | 1 g | $54.00 |