Molecular structure of 3-Ethynylpyridine, CAS Number: 2510-23-8
3-Ethynylpyridine (CAS 2510-23-8)
Application:
3-Ethynylpyridine is an alkyne substituted pyridine compound for proteomics research
CAS Number:
2510-23-8
Molecular Weight:
103.12
Molecular Formula:
C7H5N
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
3-Ethynylpyridine is an alkyne substituted pyridine compound for proteomics research. Used to prepare palladium complexes. 3-Ethynylpyridine has also been investigated for its use in x-ray crystal structures and vibrational spectroscopy studies. Additionally, it has been shown that 3-ethynylpyridine can be used as a ligand for palladium-catalyzed coupling reactions.
3-Ethynylpyridine (CAS 2510-23-8) References
- The study of secondary effects in vibrational and hydrogen bonding properties of 2- and 3-ethynylpyridine and ethynylbenzene by IR spectroscopy. | Vojta, D., et al. 2014. Spectrochim Acta A Mol Biomol Spectrosc. 132: 215-24. PMID: 24866088
- Exo-Functionalized Metallacages as Host-Guest Systems for the Anticancer Drug Cisplatin. | Woods, B., et al. 2019. Front Chem. 7: 68. PMID: 30834242
- Discovery of a Novel Series of Potent and Selective Alkynylthiazole-Derived PI3Kγ Inhibitors. | Bandarage, UK., et al. 2021. ACS Med Chem Lett. 12: 129-135. PMID: 33488974
- Photo-induced copper-catalyzed alkynylation and amination of remote unactivated C(sp3)-H bonds. | Cao, Z., et al. 2021. Chem Sci. 12: 4836-4840. PMID: 34163735
- The Influence of Secondary Interactions on the [N-I-N]+ Halogen Bond. | Lindblad, S., et al. 2021. Chemistry. 27: 13748-13756. PMID: 34339075
- Polymer-Supported-Cobalt-Catalyzed Regioselective Cyclotrimerization of Aryl Alkynes. | Sen, A., et al. 2021. JACS Au. 1: 2080-2087. PMID: 34841419
- Alternative approaches utilizing click chemistry to develop next-generation analogs of solithromycin. | Daher, SS., et al. 2022. Eur J Med Chem. 233: 114213. PMID: 35240514
- Highly-fluorescent BODIPY-functionalised metallacages as drug delivery systems: synthesis, characterisation and cellular accumulation studies. | Aikman, B., et al. 2022. Dalton Trans. 51: 7476-7490. PMID: 35470841
- Bistriazoles Connected Through a B-B Bridge, Synthesized by Highly Selective Dipolar Cycloaddition Reactions of a Diazido-diborane(4). | Vogler, D., et al. 2022. Chemistry. 28: e202201389. PMID: 35703332
- Deactivation of catalysts in simultaneous reversible and irreversible parahydrogen NMR signal enhancement, and the role of co-ligands in the stabilization of the reversible method. | Mames, A., et al. 2022. RSC Adv. 12: 15986-15991. PMID: 35733673
- Catalytic activity and mechanistic investigation of 1D 2-Picolinic acid based Cu(II) coordination polymer in the selective construction of 1,4-disubstituted triazoles. | Aier, M., et al. 2022. Sci Rep. 12: 14613. PMID: 36028653
- Palladium Nanoparticles from Desulfovibrio alaskensis G20 Catalyze Biocompatible Sonogashira and Biohydrogenation Cascades. | Era, Y., et al. 2022. JACS Au. 2: 2446-2452. PMID: 36465541
- Structure-Based Design of Y-Shaped Covalent TEAD Inhibitors. | Lu, W., et al. 2023. J Med Chem. 66: 4617-4632. PMID: 36946421
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Ethynylpyridine, 1 g | sc-231690 | 1 g | $58.00 |