Isonicotinoyl chloride hydrochloride (CAS 39178-35-3)
QUICK LINKS
Isonicotinoyl chloride hydrochloride is a chemical compound that functions as an acylating agent in organic synthesis. It is used to introduce the isonicotinoyl group into various organic molecules, allowing for the modification of their chemical properties. The compound′s mechanism of action involves the acylation of nucleophilic functional groups, such as amines and alcohols, through the formation of covalent bonds. This reaction occurs at the molecular level, leading to the formation of new compounds with altered reactivity and properties. Isonicotinoyl chloride hydrochloride serves as a reagent for the synthesis of diverse organic compounds, enabling the exploration of new chemical structures and potential applications. Its mechanism of action involves the selective acylation of specific functional groups, contributing to the diversification of chemical libraries and the discovery of novel molecules with unique properties.
Isonicotinoyl chloride hydrochloride (CAS 39178-35-3) References
- Interwoven 2-D coordination network prepared from the molecular host tris(isonicotinoyl)cyclotriguaiacylene and silver(I) cobalt(III) bis(dicarbollide). | Hardie, MJ. and Sumby, CJ. 2004. Inorg Chem. 43: 6872-4. PMID: 15500318
- Synthesis and biological evaluation of a series of novel inhibitor of Nek2/Hec1 analogues. | Qiu, XL., et al. 2009. J Med Chem. 52: 1757-67. PMID: 19243176
- Methyl 4-isonicotinamido-benzoate monohydrate. | Zhang, Y. and Zhao, XL. 2010. Acta Crystallogr Sect E Struct Rep Online. 66: o1898. PMID: 21588232
- Butane-1,4-diyl bis-(pyridine-4-carboxyl-ate). | Muthukumaran, J., et al. 2011. Acta Crystallogr Sect E Struct Rep Online. 67: o1803. PMID: 21837176
- Anticancer Activity of Self-Assembled Molecular Rectangles via Arene-Ruthenium Acceptors and a New Unsymmetrical Amide Ligand. | Mishra, A., et al. 2012. Organometallics. 31: 3519-3526. PMID: 22639481
- Butane-1,4-diyl bis-(pyridine-3-carboxyl-ate). | Vallejos, J., et al. 2012. Acta Crystallogr Sect E Struct Rep Online. 68: o2007. PMID: 22807836
- Single-Pot Self-Assembly of Heteroleptic Mn(I)-Based Aminoquinonato-Bridged Ester/Amide-Functionalized Dinuclear Metallastirrups: Potential Anticancer and Visible-Light-Triggered CORMs. | Divya, D., et al. 2019. ACS Omega. 4: 12790-12802. PMID: 31460403
- Ring Distortion of Vincamine Leads to the Identification of Re-Engineered Antiplasmodial Agents. | Norwood, VM., et al. 2021. ACS Omega. 6: 20455-20470. PMID: 34395993
- Ruthenium Olefin Metathesis Catalysts Featuring N-Heterocyclic Carbene Ligands Tagged with Isonicotinic and 4-(Dimethylamino)benzoic Acid Rests: Evaluation of a Modular Synthetic Strategy. | Czarnocki, S., et al. 2021. Molecules. 26: PMID: 34500654
- Predicting the Conformation of Organic Catalysts Grafted on Silica Surfaces with Different Numbers of Tethering Chains: The Silicopodality Concept. | Miletto, I., et al. 2021. J Phys Chem C Nanomater Interfaces. 125: 21199-21210. PMID: 34621460
- Ultrasound Irradiation Assisted Synthesis of Luminescent Nano Amide-Functionalized Metal-Organic Frameworks; Application Toward Phenol Derivatives Sensing. | Yan, XW., et al. 2022. Front Chem. 10: 855886. PMID: 35372287
- Unusual adsorption behaviours and responsive structural dynamics via selective gate effects of an hourglass porous metal-organic framework. | Xiong, Y., et al. 2019. RSC Adv. 9: 37222-37231. PMID: 35542309
- Synthesis and antifungal activity of slow-release pyridinylcarbonyl chitooligosaccharide copper complexes. | Liu, W., et al. 2022. Carbohydr Polym. 291: 119663. PMID: 35698358
- Stability of sample extracts of vitamin D3 metabolites after chemical derivatization for LC-MS/MS analysis. | Alexandridou, A. and Volmer, DA. 2023. Anal Bioanal Chem. 415: 327-333. PMID: 36342509
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Isonicotinoyl chloride hydrochloride, 5 g | sc-235408 | 5 g | $22.00 |