Interesting facts
Interesting Facts about 4-benzylpyridine
4-benzylpyridine is a fascinating compound that offers a wealth of insights into its chemical behavior and potential applications. Here are some key points to consider:
- Structure: This compound is characterized by a pyridine ring, which is an aromatic heterocycle containing nitrogen. The benzyl group provides additional stability and reactivity characteristics, making it a unique structure.
- Chemical Reactivity: The presence of the nitrogen atom in the pyridine ring adds basicity to the compound, allowing it to participate in various chemical reactions. It can act as a nucleophile in substitution reactions.
- Biological Significance: Compounds with a pyridine structure, including 4-benzylpyridine, have shown various biological activities. They are often investigated for their effectiveness as drugs, especially in neuroscience and cancer treatments.
- Applications: Beyond its biological relevance, 4-benzylpyridine is used in the synthesis of more complex molecules in organic chemistry. It stands as a valuable intermediate in the production of agrochemicals and pharmaceuticals.
- Pyridine Derivative Family: As a member of the pyridine derivative family, 4-benzylpyridine often shares properties with other pyridine compounds. Its derivatives may exhibit different pharmacological effects, highlighting the importance of structural modifications.
In the words of chemist Jean-Marie Lehn, “Molecular machines are not just a dream of the future but a reality made possible by the synergy of organic and inorganic chemistry.” 4-benzylpyridine exemplifies this synergy through its dual role in organic synthesis and potential medicinal applications.
As a chemistry student or researcher, exploring the properties and reactions of 4-benzylpyridine is an exciting venture that may contribute to future discoveries in the fields of pharmaceuticals and materials science.
Synonyms
4-BENZYLPYRIDINE
Pyridine, 4-(phenylmethyl)-
Pyridine, 4-benzyl-
gamma-Benzylpyridine
Ba 33216
.gamma.-Benzylpyridine
EINECS 218-319-0
1P29GQM0OH
NSC 8075
NSC-8075
UNII-1P29GQM0OH
BRN 0115831
AI3-19229
DTXSID5062188
5-20-07-00561 (Beilstein Handbook Reference)
PHENIRAMINE MALEATE IMPURITY B [EP IMPURITY]
PHENIRAMINE MALEATE IMPURITY B (EP IMPURITY)
DTXCID4036437
218-319-0
dbolxxrvifgdti-uhfffaoysa-n
inchi=1/c12h11n/c1-2-4-11(5-3-1)10-12-6-8-13-9-7-12/h1-9h,10h
2116-65-6
4-Benzyl-pyridine
4-(phenylmethyl)pyridine
MFCD00006443
CHEMBL357322
?-Benzylpyridine
4-benzyl pyridine
3QO
Pheniramine Maleate Imp. B (EP); Pheniramine Imp. B (EP); 4-Benzylpyridine; Pheniramine Maleate Impurity B; Pheniramine Impurity B
4-Benzylpyridine, 98%
phenyl-(4-pyridinyl)methane
WLN: T6NJ D1R
SCHEMBL432308
NSC8075
HMS3749K07
CS-B1740
BDBM50123254
AKOS000119387
FB45781
AS-56750
DB-045504
B0437
NS00026801
EN300-20244
D88648
A815178
Q27252702
Z104477464
Solubility of 4-benzylpyridine
4-benzylpyridine, with its chemical formula C11H12N, displays unique solubility characteristics that are important for various applications. This compound is primarily known for its solubility in organic solvents, and several key points illustrate its behavior:
In summary, while 4-benzylpyridine shows promising solubility in many organic solvents, it remains largely insoluble in water, highlighting its utility in organic synthesis and other chemical processes.