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4”-PROPYL-3-FLUOROBIPHENYL-4-BORONIC ACID CAS:909709-42-8

4”-Propyl-3-fluorobiphenyl-4-boronic acid is a boronic acid derivative with a molecular structure consisting of a boronic acid group attached to a biphenyl ring substituted with both propyl and fluorine functional groups. This compound plays a significant role in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile boronic acid reagent. Additionally, its specific combination of substituents provides opportunities for tailored reactivity, making it valuable in medicinal chemistry, materials science, and the synthesis of functionalized organic molecules.


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Application and Effect:

4''-Propyl-3-fluorobiphenyl-4-boronic acid is a compound with unique structural features and diverse applications across various domains of chemistry. 1. Synthetic Chemistry: Suzuki-Miyaura Cross-Coupling: This compound is extensively utilized in Suzuki-Miyaura cross-coupling reactions, enabling the construction of biaryl compounds. Its versatility as a boronic acid reagent facilitates the synthesis of complex organic molecules with potential applications in pharmaceuticals, agrochemicals, and materials science. 2. Medicinal Chemistry: Drug Development: The specific arrangement of substituents in 4''-propyl-3-fluorobiphenyl-4-boronic acid can influence its interaction with biological targets, making it valuable in drug discovery and development. Derivatives of this compound are explored for their potential as therapeutic agents targeting various diseases, including cancer, neurological disorders, and inflammation. Fluorinated Pharmaceuticals: The presence of a fluorine substituent enhances the pharmacokinetic properties and metabolic stability of drugs, making fluorinated compounds desirable in medicinal chemistry for improving drug efficacy and reducing side effects. 3. Materials Science: Functionalized Polymers: 4''-Propyl-3-fluorobiphenyl-4-boronic acid derivatives are incorporated into polymers to impart specific properties, such as enhanced solubility, conductivity, or optical properties. These functionalized polymers find applications in electronic devices, coatings, and biomedical materials. Liquid Crystals: Biphenyl derivatives, including those containing boronic acid groups, exhibit liquid crystalline behavior, making them useful in the design of liquid crystal displays (LCDs) and other optoelectronic devices. 4. Organic Synthesis: Functional Group Tolerance: The propyl and fluorine substituents on the biphenyl ring provide unique reactivity profiles, allowing for selective transformations and functional group compatibility in organic synthesis. This versatility enables the preparation of complex molecules with tailored properties and functionalities. In summary, 4''-Propyl-3-fluorobiphenyl-4-boronic acid is a versatile compound with wide-ranging applications in synthetic chemistry, medicinal chemistry, materials science, and organic synthesis. Its distinct structural features and reactivity offer opportunities for innovation and advancement in various scientific disciplines, contributing to the development of new molecules, materials, and pharmaceutical agents.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C15H16BFO2
Assay 99%
Appearance white powder
CAS No.  909709-42-8
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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