Cas no 86324-50-7 (6-Fluoroquinoline-2-carbonitrile)
6-Fluoroquinoline-2-carbonitrile Chemical and Physical Properties
Names and Identifiers
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- 6-Fluoroquinoline-2-carbonitrile
- A863242
- DTXSID10856919
- SB67979
- 86324-50-7
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- Inchi: 1S/C10H5FN2/c11-8-2-4-10-7(5-8)1-3-9(6-12)13-10/h1-5H
- InChI Key: PZYCXKQUSFWWJH-UHFFFAOYSA-N
- SMILES: FC1C=CC2C(=CC=C(C#N)N=2)C=1
Computed Properties
- Exact Mass: 172.04367633g/mol
- Monoisotopic Mass: 172.04367633g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 13
- Rotatable Bond Count: 0
- Complexity: 232
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.7
- Topological Polar Surface Area: 36.7?2
6-Fluoroquinoline-2-carbonitrile Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A189005061-1g |
6-Fluoroquinoline-2-carbonitrile |
86324-50-7 | 95% | 1g |
$478.74 | 2023-08-31 | |
| Chemenu | CM143466-1g |
6-Fluoroquinoline-2-carbonitrile |
86324-50-7 | 95% | 1g |
$549 | 2021-08-05 | |
| Chemenu | CM143466-1g |
6-Fluoroquinoline-2-carbonitrile |
86324-50-7 | 95% | 1g |
$*** | 2023-05-29 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1744378-1g |
6-Fluoroquinoline-2-carbonitrile |
86324-50-7 | 98% | 1g |
¥3906.00 | 2024-04-28 | |
| Ambeed | A707921-1g |
6-Fluoroquinoline-2-carbonitrile |
86324-50-7 | 95+% | 1g |
$465.0 | 2025-04-16 |
6-Fluoroquinoline-2-carbonitrile Related Literature
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Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
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Eunhak Lim,Jiyoung Heo,Seong Keun Kim Nanoscale, 2019,11, 11369-11378
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Hailing Chen,Lu Yin,Meng Liu,Laibing Wang,Michiya Fujiki,Wei Zhang RSC Adv., 2019,9, 4849-4856
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Doug Ogrin,Laura H. van Poppel,Simon G. Bott,Andrew R. Barron Dalton Trans., 2004, 3689-3694
Additional information on 6-Fluoroquinoline-2-carbonitrile
6-Fluoroquinoline-2-carbonitrile: A Comprehensive Overview
6-Fluoroquinoline-2-carbonitrile (CAS No. 86324-50-7) is a highly specialized organic compound that has garnered significant attention in the fields of pharmaceutical chemistry, materials science, and agrochemical research. This compound, characterized by its unique structure featuring a fluorine atom at the 6-position and a cyano group at the 2-position of the quinoline ring, exhibits remarkable chemical versatility and biological activity. Recent advancements in synthetic methodologies and its application in drug discovery have further solidified its position as a key molecule in modern chemical research.
The synthesis of 6-Fluoroquinoline-2-carbonitrile involves a series of well-defined steps, including Friedlander-type cyclization reactions and subsequent functionalization. Researchers have explored various strategies to optimize the synthesis process, ensuring high yields and purity. For instance, recent studies have highlighted the use of microwave-assisted synthesis to accelerate reaction times while maintaining product quality. Such innovations underscore the compound's importance in both academic and industrial settings.
One of the most compelling aspects of 6-Fluoroquinoline-2-carbonitrile is its potential as a lead compound in drug development. The quinoline scaffold is well-known for its pharmacological properties, and the introduction of fluorine and cyano groups further enhances its bioactivity. Recent research has demonstrated that this compound exhibits potent anti-tumor activity, particularly in inhibiting key enzymes involved in cancer progression. Additionally, its ability to modulate cellular signaling pathways makes it a promising candidate for targeted therapies.
In terms of applications, 6-Fluoroquinoline-2-carbonitrile has found utility in diverse areas such as agrochemicals, where it serves as an effective precursor for fungicides and insecticides. Its ability to interact with specific molecular targets in pests and pathogens highlights its potential in sustainable agriculture. Furthermore, the compound has been employed in materials science for the development of advanced materials with unique electronic properties.
The market demand for 6-Fluoroquinoline-2-carbonitrile has seen a steady rise due to its expanding applications across various industries. According to recent market analyses, the demand is driven by increasing investments in drug discovery programs targeting rare diseases and unmet medical needs. Moreover, the growing emphasis on green chemistry has led to innovative approaches for synthesizing this compound with reduced environmental impact.
From a regulatory standpoint, 6-Fluoroquinoline-2-carbonitrile complies with international standards for chemical safety and handling. Its production processes adhere to strict guidelines to ensure worker safety and minimize environmental hazards. Ongoing research into its toxicological profile aims to further enhance its safety profile for therapeutic applications.
In conclusion, 6-Fluoroquinoline-2-carbonitrile (CAS No. 86324-50-7) stands as a testament to the ingenuity of modern chemical research. Its unique structure, coupled with advancements in synthetic techniques and biological applications, positions it as a pivotal molecule in contemporary science. As research continues to uncover new potentials for this compound, its role in driving innovation across multiple disciplines is set to grow even further.
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