page_banner

Products

8-FLUOROQUINOLINE CAS: 394-68-3

Short Description:

Catalog Number: XD93499
Cas: 394-68-3
Molecular Formula: C9H6FN
Molecular Weight: 147.15
Availability: In Stock 
Price:  
Prepack:  
Bulk Pack: Request Quote

 


Product Detail

Product Tags

Catalog Number XD93499
Product Name 8-FLUOROQUINOLINE
CAS 394-68-3
Molecular Formula C9H6FN
Molecular Weight 147.15
Storage Details Ambient

Product Specification

Appearance White powder
Assay 99% min

 

3-Bromoquinoline is an organic compound with the molecular formula C9H6BrN. It belongs to the class of brominated quinoline compounds and finds applications in several fields, including pharmaceutical, agrochemical, and material science industries.One of the primary uses of 3-Bromoquinoline is as a building block for the synthesis of various pharmaceutical compounds. The bromine substituent attached to the quinoline ring allows for further functionalization, making it a versatile starting material. By modifying the bromine position or introducing additional functional groups, chemists can design and synthesize molecules with desired pharmacological properties. 3-Bromoquinoline derivatives have been investigated for their potential as anticancer, antiviral, and antibacterial agents. Their ability to target specific biological pathways and interact with disease-causing molecules makes them valuable in drug discovery efforts.3-Bromoquinoline also plays a significant role in the field of agrochemical research and development. It serves as an intermediate in the synthesis of crop protection chemicals, including fungicides, insecticides, and herbicides. The presence of the bromine group allows chemists to modify the compound's structure to enhance its bioactivity and specificity. By incorporating 3-Bromoquinoline derivatives into agrochemical formulations, researchers aim to develop efficient pest control measures and improve crop yields.Furthermore, 3-Bromoquinoline has applications in material science and as an intermediate in the synthesis of specialty chemicals. Its unique aromatic structure and halogen substituent make it useful for constructing complex organic frameworks. Chemical modifications of the bromine position can lead to the formation of functionalized quinoline derivatives with desirable properties, such as fluorescence, electron-accepting or electron-donating properties, or photoconductivity. These properties contribute to the development of materials for electronic, optical, and sensory applications.Additionally, 3-Bromoquinoline is employed as a reference compound and standard in analytical chemistry. It can be used for the identification and quantification of quinoline derivatives in samples, particularly in chromatographic techniques.In summary, 3-Bromoquinoline is a versatile compound with applications in pharmaceutical, agrochemical, material science, and analytical chemistry. Its ability to serve as a building block for the synthesis of diverse pharmaceutical compounds and crop protection chemicals makes it valuable in drug discovery and agrochemical research. Furthermore, its unique structure allows for the development of specialty chemicals and materials with tailored properties. This compound's diverse range of uses contributes to advancements in various scientific and industrial fields.


  • Previous:
  • Next:

  • Close

    8-FLUOROQUINOLINE CAS: 394-68-3