Cas no 2089046-86-4 (3-(3-Fluoropyridin-2-yl)propan-1-ol)

3-(3-Fluoropyridin-2-yl)propan-1-ol is a fluorinated pyridine derivative with a propanol side chain, offering versatile utility in pharmaceutical and agrochemical synthesis. The fluorine substitution at the 3-position enhances its reactivity and binding affinity, making it a valuable intermediate for designing bioactive molecules. Its hydroxyl group provides a functional handle for further derivatization, enabling the construction of more complex structures. The compound exhibits favorable solubility in common organic solvents, facilitating its use in diverse reaction conditions. Its well-defined structure and high purity make it suitable for research and development applications, particularly in medicinal chemistry where fluorinated analogs are often sought for their improved metabolic stability and selectivity.
3-(3-Fluoropyridin-2-yl)propan-1-ol structure
2089046-86-4 structure
Product Name:3-(3-Fluoropyridin-2-yl)propan-1-ol
CAS No:2089046-86-4
MF:C8H10FNO
MW:155.169505596161
CID:5524565
PubChem ID:134462777
Update Time:2025-05-22

3-(3-Fluoropyridin-2-yl)propan-1-ol Chemical and Physical Properties

Names and Identifiers

    • 3-(3-Fluoropyridin-2-yl)propan-1-ol
    • Inchi: 1S/C8H10FNO/c9-7-3-1-5-10-8(7)4-2-6-11/h1,3,5,11H,2,4,6H2
    • InChI Key: LXRGBHDKTNDWHE-UHFFFAOYSA-N
    • SMILES: C1(CCCO)=NC=CC=C1F

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3-(3-Fluoropyridin-2-yl)propan-1-ol Related Literature

Additional information on 3-(3-Fluoropyridin-2-yl)propan-1-ol

3-(3-Fluoropyridin-2-yl)propan-1-ol: A Comprehensive Overview

3-(3-Fluoropyridin-2-yl)propan-1-ol (CAS No. 2089046-86-4) is a versatile organic compound that has garnered significant attention in the fields of organic chemistry, pharmacology, and materials science. This compound, characterized by its unique structure featuring a fluorinated pyridine ring and a hydroxyl group, exhibits a wide range of applications and properties that make it an essential molecule in modern research and industry.

The chemical structure of 3-(3-fluoropyridin-2-yl)propan-1-ol consists of a pyridine ring substituted with a fluorine atom at the 3-position and a propanol group attached at the 2-position. This arrangement imparts the molecule with both aromaticity and hydroxyl functionality, which are key to its reactivity and utility. The compound's physical properties, including its melting point, boiling point, and solubility, have been extensively studied to optimize its use in various chemical processes.

Recent advancements in synthetic chemistry have enabled the development of efficient methods for the synthesis of 3-(3-fluoropyridin-2-yl)propan-1-ol. Researchers have explored diverse strategies, including nucleophilic aromatic substitution, coupling reactions, and catalytic hydrogenation, to achieve high yields and purity. These methods not only enhance the scalability of production but also pave the way for further functionalization of the molecule to create derivatives with tailored properties.

The biological activity of 3-(3-fluoropyridin-2-yl)propan-1-ol has been a focal point of recent studies. Investigations into its pharmacokinetics, toxicity, and interaction with biological systems have revealed promising potential in drug discovery. For instance, studies suggest that this compound may exhibit anti-inflammatory or antioxidant properties, making it a candidate for therapeutic applications. Additionally, its ability to act as an intermediate in the synthesis of more complex molecules further underscores its importance in medicinal chemistry.

In the realm of materials science, 3-(3-fluoropyridin-2-yli)propanol has shown promise as a building block for advanced materials. Its ability to participate in polymerization reactions or serve as a precursor for conducting polymers highlights its versatility. Researchers are actively exploring its potential in creating materials with enhanced electronic or mechanical properties.

From an environmental perspective, understanding the ecotoxicological impact of 3-(3-fluoropyridin-yli)propanol is crucial for sustainable practices. Studies are underway to assess its biodegradability and potential effects on aquatic ecosystems. These efforts aim to ensure that its use aligns with eco-friendly principles while maintaining its industrial relevance.

In conclusion, 3-(3-fluoropyridin-yli)propanol (CAS No. 2089046-yli) stands as a testament to the ingenuity of modern chemistry. Its multifaceted applications across various disciplines underscore its significance as both a research tool and an industrial material. As ongoing research continues to unlock new insights into its properties and potential uses, this compound is poised to play an increasingly vital role in shaping future advancements in science and technology.

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