AE16566
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 98% | in stock | $22.00 | $15.00 | - + | |
1g | 98% | in stock | $32.00 | $22.00 | - + | |
5g | 98% | in stock | $49.00 | $35.00 | - + | |
10g | 98% | in stock | $98.00 | $69.00 | - + | |
25g | 98% | in stock | $217.00 | $152.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE16566 |
Chemical Name: | 3,5-Difluoro-4-nitrobenzonitrile |
CAS Number: | 1123172-88-2 |
Molecular Formula: | C7H2F2N2O2 |
Molecular Weight: | 184.0998 |
MDL Number: | MFCD13193247 |
SMILES: | N#Cc1cc(F)c(c(c1)F)[N+](=O)[O-] |
3,5-Difluoro-4-nitrobenzonitrile is a versatile compound that finds wide application in chemical synthesis. Its unique molecular structure containing fluorine and nitro groups imparts distinct reactivity and selectivity to various reactions. In organic synthesis, this compound serves as a key building block for the preparation of complex molecules and pharmaceutical intermediates.One notable application of 3,5-Difluoro-4-nitrobenzonitrile is its role as a valuable starting material in the synthesis of fluorinated aromatic compounds. The presence of fluorine atoms on the benzene ring not only enhances the electronic properties of the molecule but also enables further functionalization to introduce a variety of substituents. This allows for the creation of novel compounds with enhanced properties and potential applications in drug discovery and materials science.Furthermore, the nitro group present in 3,5-Difluoro-4-nitrobenzonitrile can undergo various transformations such as reduction, substitution, or functional group interconversion, thereby expanding the synthetic possibilities of this compound. Through strategic manipulation of the nitro group, chemists can access a diverse array of derivatives that can be further elaborated into complex molecular architectures.Overall, the utility of 3,5-Difluoro-4-nitrobenzonitrile in chemical synthesis lies in its ability to serve as a versatile precursor for the construction of fluorinated and functionalized aromatic compounds with interesting properties and potential applications in various fields of chemistry and beyond.