2-(2,4-Difluorophenyl)-5-fluoropyridine
CAS Number 1426047-01-9
Chemistry Building Blocks, Fluorinated Building Blocks, Heterocyclic Building Blocks, Materials, Monomers
A difluorinated heterocyclic ligand
Also a well-known chelating ligand in application of APIs, OLEDs, DSSCs and photocatalytic reactions
Specifications | MSDS | Literature and Reviews
2-(2,4-Difluorophenyl)-5-fluoropyridine (DFFPPy), CAS number 1426047-01-9, normally serving as a chelating ligand, is a trifluorinated phenyl-pyridine derivative. Phenyl-pyridine building blocks are popular candidates in the synthesis of iridium complexes for catalytic photoredox reactions, assisting the formation of Ir(III)* (excited triplet state) upon visible light irradiation. 2-(2,4-Difluorophenyl)-5-fluoropyridine also shows its effectiveness for visceral leishmaniasis in preclinical screening assay. The increase lipophilicity brought by the fluorine substituents has higher potency against Leishmania infantum.
As a cyclometalating ligand used for photoemitter and being electron deficient with the help of three fluorine, DFFPPy introduces blue shift to the emission wavelength (typically by reducing the highest occupied molecular orbital energy level) and increases the photoluminescence quantum yield (from 6.5% to 50.8%).
Multiple functional groups
For facile synthesis
Fluorinated phenylpyridine building block
For drug discoveries, solar cells, and photocatalists
Worldwide shipping
Quick and reliable shipping
High purity
>98% High purity
General Information
CAS Number | 1426047-01-9 |
Chemical Formula | C12H6F3N |
Full Name | 2-(2,4-Difluorophenyl)-5-fluoropyridine |
Molecular Weight | 209.17 g/mol |
Synonyms | DFFPPy |
Classification / Family | Pyridine derivatives, Fluorinated building blocks, Heterocyclic building block, Dyes, DSSCs, Photocatalyst ligands, OLEDs |
Chemical Structure
Product Details
Purity | >98% |
Melting Point | Tm = 75 °C – 78 °C |
Appearance | White to yellow powder/crystal |
MSDS Documentation
2-(2,4-Difluorophenyl)-5-fluoropyridine MSDS Sheet
Literature and Reviews
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7-Substituted 2-nitro-5,6-dihydroimidazo[2,1-b][1,3]oxazines: novel antitubercular agents lead to a new preclinical candidate for visceral leishmaniasis, A. Tompson et al., J. Med. Chem., 60, 4212−4233(2017); DOI: 10.1021/acs.jmedchem.7b00034.
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A radical approach to the copper oxidative addition problem: trifluoromethylation of bromoarenes, C. Le et al., Science, 360(6392), 1010-1014(2018), DOI: 10.1126/science.aat4133.
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Developments in photoredox-mediated alkylation for DNA-encoded libraries, S. Patel et al., Trends Chem., 3(3), 161-175(2021); DOI: 10.1016/j.trechm.2020.11.010.