Interesting facts
Interesting Facts about 3-Chloro-N-(2-phenylethyl)propanamide
3-Chloro-N-(2-phenylethyl)propanamide is a unique chemical compound that captivates the interest of both organic chemists and pharmacologists. Here are some engaging insights about this compound:
- Functional Group Variety: This compound belongs to the amide class, distinguished by the presence of a carbonyl group linked to a nitrogen atom. The incorporation of the aromatic phenylethyl group adds complexity to its structure, influencing its reactivity and interactions.
- Potential Biological Activity: Compounds containing amide linkages are often found in bioactive molecules. It is noted that derivatives of such amides may exhibit interesting biological properties, including anti-inflammatory and analgesic effects.
- Synthesis and Applications: The synthesis of 3-chloro-N-(2-phenylethyl)propanamide can involve several methods in organic chemistry, showcasing the versatility of synthetic techniques. Its applications may extend into medicinal chemistry, where it can serve as a scaffold for drug development initiatives.
- Substituent Effects: The presence of the Cl (chlorine) substituent is notable. Chlorination often alters the electronic properties of compounds, affecting how they interact with biological targets. This can make the compound a focal point in studies geared toward developing novel pharmaceuticals.
- Reactivity: As an amide, it may undergo hydrolysis and other reactions characteristic of functional groups that can be further explored for synthetic innovation.
In summary, 3-chloro-N-(2-phenylethyl)propanamide epitomizes the fascinating interplay between structure and function in organic chemistry. The potential for biological activity and its applications in drug development make it a compound worth studying in greater detail for future scientific exploration.
Synonyms
Fenaclon
306-20-7
Fenaclonum
3-Chloro-N-(2-phenylethyl)propanamide
Phenacon
Fenakon
Phenacone
Fenaclon [INN]
Fenaclone
3-Chloro-N-phenethylpropionamide
Fenaclona
Fenaclone [INN-French]
Fenaclonum [INN-Latin]
Fenaclona [INN-Spanish]
N-(2-Phenethyl)-3-chloropropionamide
3-Chloro-N-phenethyl-propionamide
Propanamide, 3-chloro-N-(2-phenylethyl)-
UNII-6M4IR9QY13
BRN 2939383
6M4IR9QY13
DTXSID0057708
DTXCID8031497
PROPIONAMIDE, 3-CHLORO-N-(PHENETHYL)-
4-12-00-02464 (Beilstein Handbook Reference)
Propionamide, 3-chloro-N-phenethyl-
.beta.-Chloro-N-phenethylpropionamide
.beta.-Chloropropio-N-phenylethylamide
Fenaclone (INN-French)
Fenaclonum (INN-Latin)
Fenaclona (INN-Spanish)
SCHEMBL2109480
CHEMBL2106620
beta-Chloro-N-phenethylpropionamide
AAA30620
beta-Chloropropio-N-phenylethylamide
HY-B1097
Tox21_113856
AKOS000144721
CCG-213905
CS-4686
NCGC00253738-01
3-Chloro-N-(2-phenylethyl)propanamide #
CAS-306-20-7
TS-09849
NS00120407
EN300-57073
VU0549352-1
G22280
AB01563363_01
Propanamide, 3-chloro-N-(2-phenylethyl)-(9CI)
SR-01000944265
SR-01000944265-1
BRD-K08791496-001-01-0
Q27265137
F9995-0372
Z240089880
Solubility of 3-chloro-N-(2-phenylethyl)propanamide
The solubility of 3-chloro-N-(2-phenylethyl)propanamide in various solvents can be categorized by considering its structural features and polar characteristics. Understanding its solubility behavior is crucial for applications in chemical synthesis and pharmaceutical formulations.
Key Factors Influencing Solubility:
Generally, amides tend to be soluble in polar solvents; however, due to the bulky phenyl group and chlorinated substituent, solubility might be limited. Common observations for this compound include:
In summary, while the solubility of 3-chloro-N-(2-phenylethyl)propanamide can be predicted by its molecular structure, actual solubility should be determined experimentally for precise applications since it can vary based on conditions such as temperature and solvent composition.