Interesting facts
Exploring 4-(4-formylphenyl)benzaldehyde
4-(4-formylphenyl)benzaldehyde, widely known for its distinctive aromatic properties, is an intriguing compound that finds its usefulness in various chemical applications. Here are some interesting facts about this fascinating molecule:
- Structure & Reactivity: This compound is characterized by its dual aldehyde groups, which can significantly influence its reactivity. The presence of the formyl and benzaldehyde functionalities makes it a key intermediate in organic synthesis, especially in the development of complex organic molecules.
- Synthetic Utility: Due to its reactive aldehyde groups, 4-(4-formylphenyl)benzaldehyde is often employed in condensation reactions and can serve as a precursor for various heterocyclic compounds, making it a valuable building block in the pharmaceutical industry.
- Colorimetric Applications: Interestingly, compounds like 4-(4-formylphenyl)benzaldehyde can have applications in developing sensors and indicators due to their ability to undergo color changes in response to chemical environments.
- Chemical Properties: The intermolecular interactions in 4-(4-formylphenyl)benzaldehyde can lead to interesting results during crystallization and polymorphism, which are important factors to consider in material science.
- Studies & Research: Research into this compound contributes to the understanding of aromatic chemistry and the design of novel materials. According to recent studies, modifying the functional groups around the benzaldehyde can yield compounds with enhanced properties, paving the way for new innovations.
In conclusion, 4-(4-formylphenyl)benzaldehyde is more than just a chemical; it is a compound that exemplifies the intersection of theoretical study and practical application. Its unique features provide ample opportunities for exploration and discovery in the world of chemistry.
Synonyms
66-98-8
4,4'-BIPHENYLDICARBOXALDEHYDE
[1,1'-biphenyl]-4,4'-dicarbaldehyde
biphenyl-4,4'-dicarbaldehyde
4-(4-formylphenyl)benzaldehyde
4,4'-Diformylbiphenyl
4,4'-Biphenyldicarboxyaldehyde
p,p'-Diformylbiphenyl
(1,1'-Biphenyl)-4,4'-dicarboxaldehyde
BRN 2254807
[1,1'-Biphenyl]-4,4'-dicarboxaldehyde
MFCD00016714
4,4'-diformyl-1,1'-biphenyl
DTXSID60216206
4-07-00-02511 (Beilstein Handbook Reference)
4,4'-bisformylbiphenyl
4,4'-Bis(formyl)biphenyl
YSWG223
4,4'-biphenyidicarboxaldehyde
SCHEMBL976904
biphenyl-4,4'-dicarboxaldehyde
DTXCID20138697
Ald3-H_000015
Ald3.1-H_000272
Ald3.1-H_000591
Ald3.1-H_000910
AKOS015840512
4 pound not4'-Biphenyldicarboxaldehyde
AC-6203
FB55014
AS-15649
SY053149
B2854
CS-0127999
NS00076522
O10236
10.14272/FEHLIYXNTWAEBQ-UHFFFAOYSA-N.1
doi:10.14272/FEHLIYXNTWAEBQ-UHFFFAOYSA-N.1
Biphenyl-4,4 inverted exclamation mark -dicarbaldehyde
Solubility of 4-(4-formylphenyl)benzaldehyde (C14H10O2)
The solubility characteristics of 4-(4-formylphenyl)benzaldehyde can be intriguing due to its organic structure and functional groups. Here are some key points regarding its solubility:
In conclusion, while 4-(4-formylphenyl)benzaldehyde may not readily dissolve in water, its affinity for non-polar solvents highlights an interesting aspect of solubility that chemists should consider when working with similar compounds. Always remember that the nature of the solvent plays a critical role in the solubility of organic compounds!