Interesting facts
Interesting Facts about Pyridine-4-Carbaldehyde
Pyridine-4-carbaldehyde, a remarkable chemical compound, is notably recognized for its versatility in organic synthesis and its distinct properties. Here are some engaging facts that highlight its significance:
- Structural Insights: This compound features a pyridine ring with a carbaldehyde group positioned at the fourth carbon. Pyridine itself is a six-membered aromatic ring, which contributes unique characteristics to the molecule.
- Key Applications: Pyridine-4-carbaldehyde is utilized as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its functional group makes it an essential building block for the creation of complex organic molecules.
- Role in Research: This compound is often employed in laboratory studies to explore its reactivity and properties. Researchers have noted its utility in catalysis and as a ligand in coordination chemistry.
- Biological Interests: Some derivatives of pyridine-4-carbaldehyde exhibit biological activity, making them subjects of interest in medicinal chemistry. They have been studied for potential anticancer and antimicrobial properties.
- Environmental Relevance: As a component in various industrial processes, understanding pyridine-4-carbaldehyde's behavior in the environment is crucial. Its potential impacts on biological systems are a topic of ongoing research.
In summary, pyridine-4-carbaldehyde serves as more than just a chemical compound; it plays a pivotal role in numerous scientific advancements. As Albert Einstein once said, "Science can flourish only in an environment of free speech." This idea is particularly relevant in the research surrounding versatile compounds like pyridine-4-carbaldehyde, where innovation thrives through exploration and discovery.
Synonyms
4-Pyridinecarboxaldehyde
Isonicotinaldehyde
Pyridine-4-carbaldehyde
4-FORMYLPYRIDINE
Isonicotinic aldehyde
4-Pyridinealdehyde
p-Pyridinealdehyde
p-Formylpyridine
4-Pyridylaldehyde
4-Pyridinecarbaldehyde
NSC 8953
Pyridine-4-aldehyde
EINECS 212-832-3
AI3-33232
NSC-8953
pyridin-4-ylcarboxaldehyde
DTXSID1061237
EC 212-832-3
P577557492
4formylpyridine
4pyridylaldehyde
pPyridinealdehyde
4Pyridinealdehyde
I3-Formylpyridine
Pyridine4carbaldehyde
Pyridine4carboxaldehyde
DTXCID3048574
bguwfuqjcdrptl-uhfffaoysa-n
inchi=1/c6h5no/c8-5-6-1-3-7-4-2-6/h1-5
872-85-5
Pyridine-4-carboxaldehyde
MFCD00006425
gamma-Formylpyridine
pyridine, 4-formyl-
4-pyridine carboxaldehyde
(4-Pyridinecarboxaldehyde)
4-picolinaldehyde
|A-Formylpyridine
NSC8953
4-Formyl-pyridine
Pyridin-4-al
piridine-4-aldehyde
pyridine 4-aldehyde
4-pyridylformaldehyde
pyridine4-carbaldehyde
4-pyrdinecarboxaldehyde
4-pyridincarboxaldehyde
4-pyridinecaboxaldehyde
4-pyridinecarboaldehyde
pyridin-4-carbaldehyde
4-pyridine carbaldehyde
4-pyridine-formaldehyde
pyridine 4-carbaldehyde
pyridine-4 carbaldehyde
pyridine-4carboxaldehyde
pyridine4-carboxaldehyde
4-pyridine carboaldehyde
pyridin-4-carboxaldehyde
4 -pyridinecarboxaldehyde
4-pyridine-carboxaldehyde
4-pyridinecarbox-aldehyde
pyridine 4-carboxaldehyde
PYRIDIN-4-ALDEHYDE
Pyridine-4-ylcarboxaldehyde
SCHEMBL28473
carbonyl-1,4-dihydropyridine
4-Pyridinecarboxaldehyde, 97%
SCHEMBL4027783
CHEMBL2251606
CS-D1135
BBL025920
STL281177
UNII-P577557492
AKOS000119727
AB00754
AC-2103
AS-30155
DB-031936
I0143
NS00003365
EN300-18111
Q23636732
Z57161993
F1294-0084
Solubility of Pyridine-4-carbaldehyde
Pyridine-4-carbaldehyde, with the chemical formula C6H5NO, exhibits distinctive solubility properties that are crucial for its various applications in organic synthesis and pharmaceuticals. Understanding its solubility can provide insights into its behavior in different environments.
Solubility Characteristics:
Overall, the solubility of pyridine-4-carbaldehyde is characterized by its compatibility with non-polar and moderately polar solvents, making it a versatile reagent in laboratory settings. As stated, "Properties of solubility can dictate the pathway of chemical reactions." Understanding these properties allows chemists to manipulate conditions for desired chemical outcomes.