Ethyl 4-iodobenzoate (CAS 51934-41-9)
QUICK LINKS
Ethyl 4-iodobenzoate functions as a reagent in organic synthesis, in the preparation of various aromatic compounds. Its mechanism of action involves participating in esterification reactions, where it acts as an electrophile, reacting with nucleophiles to form ester compounds. Ethyl 4-Iodobenzoate is also involved in the synthesis of intermediates and agrochemicals, where it serves as a building block for the construction of complex molecular structures. In this, ethyl 4-iodobenzoate undergoes substitution reactions, enabling the introduction of the iodine atom into the target molecule. Its role in the formation of carbon-carbon and carbon-heteroatom bonds may be a versatile for the creation of diverse chemical compounds. Ethyl 4-iodobenzoate′s ability to participate in these transformations contributes to the development of new materials and compounds for various industrial and applications.
Ethyl 4-iodobenzoate (CAS 51934-41-9) References
- Rapid and efficient trifluoromethylation of aromatic and heteroaromatic compounds using potassium trifluoroacetate enabled by a flow system. | Chen, M. and Buchwald, SL. 2013. Angew Chem Int Ed Engl. 52: 11628-31. PMID: 24038907
- Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines. | Osborne, CA., et al. 2015. Org Lett. 17: 5340-3. PMID: 26506430
- Functionalizations of Mixtures of Regioisomeric Aryllithium Compounds by Selective Trapping with Dichlorozirconocene. | Castelló-Micó, A., et al. 2016. Angew Chem Int Ed Engl. 55: 401-4. PMID: 26586204
- [11 C]Fluoroform, a Breakthrough for Versatile Labeling of PET Radiotracer Trifluoromethyl Groups in High Molar Activity. | Haskali, MB. and Pike, VW. 2017. Chemistry. 23: 8156-8160. PMID: 28514059
- Practical and economic lithiations of functionalized arenes and heteroarenes using Cy2NLi in the presence of Mg, Zn or La halides in a continuous flow. | Becker, MR., et al. 2015. Chem Sci. 6: 6649-6653. PMID: 29435214
- Copper-Promoted Cross-Coupling Reactions for the Synthesis of Aryl(difluoromethyl)phosphonates Using Trimethylsilyl(difluoromethyl)phosphonate. | Komoda, K., et al. 2018. Molecules. 23: PMID: 30545029
- The Asymmetric A³(Aldehyde⁻Alkyne⁻Amine) Coupling: Highly Enantioselective Access to Propargylamines. | Mo, JN., et al. 2019. Molecules. 24: PMID: 30925732
- Pyrrole-Protected β-Aminoalkylzinc Reagents for the Enantioselective Synthesis of Amino-Derivatives. | Leroux, M., et al. 2020. Chemistry. 26: 8951-8957. PMID: 32196786
- 'On Water' Palladium Catalyzed Direct Arylation of 1H-Indazole and 1H-7-Azaindazole. | Gambouz, K., et al. 2020. Molecules. 25: PMID: 32570894
- Chiral Polythiophenes: Part I: Syntheses of Monomeric Precursors. | Krasowska, D., et al. 2021. Molecules. 26: PMID: 34299480
- A One-Pot Synthesis-Functionalization Strategy for Streamlined Access to 2,5-Disubstituted 1,3,4-Oxadiazoles from Carboxylic Acids. | Matheau-Raven, D. and Dixon, DJ. 2022. J Org Chem. 87: 12498-12505. PMID: 36054913
- Enantioselective nickel-catalyzed dicarbofunctionalization of 3,3,3-trifluoropropene. | Li, YZ., et al. 2022. Nat Commun. 13: 5539. PMID: 36130927
- Folic Acid Antimetabolites (Antifolates): A Brief Review on Synthetic Strategies and Application Opportunities. | Kovalev, IS., et al. 2022. Molecules. 27: PMID: 36234766
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Ethyl 4-iodobenzoate, 5 g | sc-257474 | 5 g | $57.00 |