logo
Home  > 1,3-Benzenedicarbonitrile, 4,6-difluoro-

AX24466

17654-70-5 | 1,3-Benzenedicarbonitrile, 4,6-difluoro-

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $36.00 $25.00 -   +
1g 95% in stock $141.00 $99.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AX24466
Chemical Name: 1,3-Benzenedicarbonitrile, 4,6-difluoro-
CAS Number: 17654-70-5
Molecular Formula: C8H2F2N2
Molecular Weight: 164.1117
MDL Number: MFCD19440215
SMILES: N#Cc1cc(C#N)c(cc1F)F

 

Computed Properties
Complexity: 233  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 4  
XLogP3: 1.6  

 

 

Upstream Synthesis Route
  • 4,6-Difluoro-1,3-benzenedicarbonitrile, also known as DFBDC, is a valuable building block in chemical synthesis due to its versatile application in organic chemistry. This compound serves as a key intermediate in the preparation of various functionalized organic molecules, especially in the pharmaceutical and agrochemical industries.One of the primary uses of 4,6-Difluoro-1,3-benzenedicarbonitrile is its role as a precursor in the synthesis of heterocyclic compounds. By undergoing cyclization reactions with appropriate reagents, DFBDC can be transformed into a range of heterocycles such as pyrazoles, pyrimidines, and triazoles. These heterocyclic derivatives are important structural motifs found in many bioactive molecules, making DFBDC a valuable starting material for medicinal chemistry research.Furthermore, 4,6-Difluoro-1,3-benzenedicarbonitrile is commonly employed in the synthesis of fluorinated organic compounds. The presence of fluorine atoms in the molecule imparts unique properties such as increased lipophilicity, metabolic stability, and bioavailability. As a result, DFBDC derivatives find applications as potential drug candidates, agrochemicals, and materials in various industries.In addition to its use in heterocyclic and fluorine chemistry, 4,6-Difluoro-1,3-benzenedicarbonitrile can also participate in cross-coupling reactions to introduce functional groups at the difluorophenyl ring. This versatility enables the incorporation of diverse chemical moieties into the DFBDC framework, expanding the scope of potential applications in chemical synthesis.Overall, the strategic incorporation of 4,6-Difluoro-1,3-benzenedicarbonitrile in organic synthesis enables the efficient construction of complex molecules with diverse functionalities, making it a valuable tool for researchers and chemists in the development of novel compounds for various purposes.
FEATURED PRODUCTS