Introduction of CAS:136516-64-8 | Benzaldehyde, 2,4-difluoro-6-hydroxy- (9CI)
The molecular structure of benzaldehydes can be quite complex, with intramolecular hydrogen bonding and planar configurations being common features. For example, 2,4-Dihydroxybenzaldehyde forms sheets with intermolecular hydrogen bonds, and its molecules are characterized by an intramolecular hydrogen bond . The presence of substituents like fluorine in 2,4-Difluoro-6-hydroxybenzaldehyde would likely influence its molecular geometry and intermolecular interactions, potentially leading to unique structural motifs.
Specification of CAS:136516-64-8 | Benzaldehyde, 2,4-difluoro-6-hydroxy- (9CI)
|
ITEMS |
SPECIFICATION |
|
Melt point |
32℃ |
|
Boiling point |
207.6±35.0 °C(Predicted) |
|
Density |
1.464±0.06 g/cm3(Predicted) |
|
Purity |
97% |
|
Storage condition |
under inert gas (nitrogen or Argon) at 2-8°C |
Research Application of CAS:136516-64-8 | Benzaldehyde, 2,4-difluoro-6-hydroxy- (9CI)
Reaction and Catalysis
2-Hydroxybenzaldehydes, closely related to 2,4-Difluoro-6-hydroxybenzaldehyde, efficiently react with alkynes, alkenes, or allenes, facilitated by a rhodium-based catalyst system. This reaction involves the cleavage of the aldehyde C-H bond, leading to the formation of 2-alkenoylphenols (Kokubo et al., 1999).
Organic Synthesis
Electron-rich benzaldehyde derivatives, such as 2,4-dihydroxybenzaldehyde, are used as linkers for solid-phase organic synthesis. They undergo reductive amination and further derivatization to form various amide compounds (Swayze, 1997).
Cu(OAc)2 catalyzes the oxyfunctionalization of 4-hydroxybenzaldehydes and derivatives, converting them into various aromatic carbonyl compounds. This process is significant for pharmaceutical applications due to the importance of 4-hydroxybenzaldehydes and 4-hydroxyphenones (Jiang et al., 2014).



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