Cas no 1427501-46-9 (6-Fluoroisoquinoline-1-carbonitrile)
6-Fluoroisoquinoline-1-carbonitrile Chemical and Physical Properties
Names and Identifiers
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- 6-FLUOROISOQUINOLINE-1-CARBONITRILE
- 6-Fluoroisoquinoline-1-carbonitrile
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- Inchi: 1S/C10H5FN2/c11-8-1-2-9-7(5-8)3-4-13-10(9)6-12/h1-5H
- InChI Key: NNBWOMQUXWHJMO-UHFFFAOYSA-N
- SMILES: FC1C=CC2C(C#N)=NC=CC=2C=1
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 13
- Rotatable Bond Count: 0
- Complexity: 232
- XLogP3: 2.3
- Topological Polar Surface Area: 36.7
6-Fluoroisoquinoline-1-carbonitrile Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM229043-1g |
6-Fluoroisoquinoline-1-carbonitrile |
1427501-46-9 | 97% | 1g |
$425 | 2021-08-04 | |
| Alichem | A189009456-1g |
6-Fluoroisoquinoline-1-carbonitrile |
1427501-46-9 | 95% | 1g |
$464.10 | 2022-04-02 | |
| Chemenu | CM229043-1g |
6-Fluoroisoquinoline-1-carbonitrile |
1427501-46-9 | 97% | 1g |
$*** | 2023-03-30 |
6-Fluoroisoquinoline-1-carbonitrile Related Literature
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
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Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
Additional information on 6-Fluoroisoquinoline-1-carbonitrile
Comprehensive Overview of 6-Fluoroisoquinoline-1-carbonitrile (CAS No. 1427501-46-9): Properties, Applications, and Industry Insights
6-Fluoroisoquinoline-1-carbonitrile (CAS No. 1427501-46-9) is a fluorinated heterocyclic compound that has garnered significant attention in pharmaceutical and agrochemical research due to its unique structural features. The presence of both a fluorine atom and a nitrile group in the isoquinoline backbone makes it a versatile intermediate for synthesizing bioactive molecules. This compound is particularly valued for its potential in drug discovery, where its electron-withdrawing properties and hydrogen-bond acceptor capabilities enhance binding affinity to biological targets.
Recent studies highlight the growing demand for fluorinated isoquinoline derivatives in medicinal chemistry, driven by their ability to improve metabolic stability and bioavailability. Researchers are actively exploring 6-Fluoroisoquinoline-1-carbonitrile as a precursor for kinase inhibitors and G-protein-coupled receptor (GPCR) modulators, aligning with the industry's focus on precision therapeutics. The compound's CAS No. 1427501-46-9 is frequently searched in scientific databases, reflecting its relevance in high-throughput screening and fragment-based drug design.
From a synthetic perspective, 6-Fluoroisoquinoline-1-carbonitrile offers advantages in palladium-catalyzed cross-coupling reactions, enabling the construction of complex molecular architectures. Its nitrile group serves as a handle for further functionalization, while the fluorine atom influences lipophilicity and membrane permeability—key parameters in optimizing drug candidates. These attributes resonate with current trends in AI-driven molecular modeling, where researchers prioritize compounds with tunable physicochemical properties.
Environmental and regulatory considerations also shape the discourse around 1427501-46-9. As sustainable chemistry gains traction, innovations in green fluorination methods for synthesizing such compounds are being widely discussed. The compound's stability under physiological conditions makes it a candidate for prodrug development, addressing challenges in targeted drug delivery—a hot topic in nanomedicine forums.
In agrochemical applications, 6-Fluoroisoquinoline-1-carbonitrile derivatives show promise as plant growth regulators and pest control agents. Its structural motif appears in patents for herbicides with improved selectivity, catering to the demand for eco-friendly crop protection solutions. This dual applicability in pharma and agro sectors underscores its commercial potential, with global market reports projecting growth for fluorinated heterocycles.
Analytical characterization of CAS No. 1427501-46-9 typically involves HPLC purity analysis, mass spectrometry, and NMR spectroscopy—techniques frequently queried in academic and industrial workflows. The compound's spectral data (e.g., 19F-NMR chemical shifts) are critical for quality control, especially in contract research organizations (CROs) servicing the drug development pipeline.
Emerging discussions in open-access chemistry journals emphasize the need for scalable synthesis routes for fluorinated nitriles like 6-Fluoroisoquinoline-1-carbonitrile. Recent breakthroughs in continuous flow chemistry and electrochemical fluorination are reducing production costs, making such compounds more accessible for academic labs and startups.
In summary, 6-Fluoroisoquinoline-1-carbonitrile (CAS No. 1427501-46-9) exemplifies the intersection of structural innovation and practical utility in modern chemistry. Its multifaceted applications—from small-molecule therapeutics to sustainable agriculture—position it as a compound of enduring scientific and industrial interest, meriting continued exploration in peer-reviewed literature and patent filings worldwide.
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