Cas no 1379304-08-1 (3-(3-bromo-5-fluorophenoxy)propanenitrile)

3-(3-bromo-5-fluorophenoxy)propanenitrile structure
1379304-08-1 structure
Product Name:3-(3-bromo-5-fluorophenoxy)propanenitrile
CAS No:1379304-08-1
MF:C9H7BrFNO
MW:244.060384988785
MDL:MFCD18911597
CID:5169682
Update Time:2026-03-04

3-(3-bromo-5-fluorophenoxy)propanenitrile Chemical and Physical Properties

Names and Identifiers

    • 3-(3-bromo-5-fluorophenoxy)propanenitrile
    • MDL: MFCD18911597
    • Inchi: 1S/C9H7BrFNO/c10-7-4-8(11)6-9(5-7)13-3-1-2-12/h4-6H,1,3H2
    • InChI Key: VAGXSHIHJXEHQA-UHFFFAOYSA-N
    • SMILES: C(#N)CCOC1=CC(F)=CC(Br)=C1

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3

3-(3-bromo-5-fluorophenoxy)propanenitrile Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB433004-1 g
3-(3-Bromo-5-fluoro-phenoxy)propanenitrile; .
1379304-08-1
1g
€1,621.80 2023-04-23
abcr
AB433004-1g
3-(3-Bromo-5-fluoro-phenoxy)propanenitrile; .
1379304-08-1
1g
€1555.10 2025-03-19

Additional information on 3-(3-bromo-5-fluorophenoxy)propanenitrile

Comprehensive Overview of 3-(3-bromo-5-fluorophenoxy)propanenitrile (CAS No. 1379304-08-1)

3-(3-bromo-5-fluorophenoxy)propanenitrile (CAS No. 1379304-08-1) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research and material science. This compound, characterized by its unique bromo-fluorophenoxy and propanenitrile functional groups, serves as a versatile intermediate in the synthesis of more complex molecules. Its molecular structure, which includes both halogenated and nitrile components, makes it particularly valuable for applications requiring precise chemical modifications.

In recent years, the demand for halogenated aromatic compounds like 3-(3-bromo-5-fluorophenoxy)propanenitrile has surged, driven by their utility in drug discovery and agrochemical development. Researchers are increasingly exploring its potential as a building block for small-molecule inhibitors and biologically active agents. The compound's electron-withdrawing properties, attributed to the fluorine and bromine atoms, enhance its reactivity in nucleophilic substitution reactions, a feature highly sought after in medicinal chemistry.

One of the most frequently asked questions about CAS No. 1379304-08-1 revolves around its synthetic pathways and purification methods. Advanced techniques such as column chromatography and recrystallization are commonly employed to achieve high purity levels, ensuring its suitability for sensitive applications. Additionally, the compound's stability under various pH conditions and thermal profiles has been extensively studied, making it a reliable choice for long-term storage and transport.

The growing interest in sustainable chemistry has also put 3-(3-bromo-5-fluorophenoxy)propanenitrile in the spotlight. Innovations in green synthesis methods, such as catalyst-free reactions and solvent-free conditions, are being explored to minimize environmental impact. This aligns with the broader industry trend toward eco-friendly and cost-effective production processes, which are increasingly prioritized by both manufacturers and end-users.

From a commercial perspective, CAS No. 1379304-08-1 is often sourced by pharmaceutical intermediates suppliers and research laboratories. Its market value is influenced by factors such as purity grade, batch size, and regulatory compliance. As the compound gains traction in high-throughput screening and combinatorial chemistry, its role in accelerating drug development pipelines cannot be overstated.

In summary, 3-(3-bromo-5-fluorophenoxy)propanenitrile (CAS No. 1379304-08-1) represents a critical tool in modern chemical research. Its multifaceted applications, coupled with ongoing advancements in synthetic methodologies, position it as a compound of enduring relevance. For researchers and industry professionals alike, understanding its properties and potential is essential for leveraging its full capabilities in innovative scientific endeavors.

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