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N-(3-chloro-4-cyano-phenyl)acetamide

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Identification
Molecular formula
C9H7ClN2O
CAS number
94533-56-9
IUPAC name
N-(3-chloro-4-cyano-phenyl)acetamide
State
State
At room temperature, N-(3-chloro-4-cyano-phenyl)acetamide is in a solid state, typically presenting itself as a crystalline powder or manageable small solid pieces.
Melting point (Celsius)
188.00
Melting point (Kelvin)
461.20
Boiling point (Celsius)
355.60
Boiling point (Kelvin)
628.80
General information
Molecular weight
194.62g/mol
Molar mass
194.6110g/mol
Density
1.3240g/cm3
Appearence

N-(3-chloro-4-cyano-phenyl)acetamide typically appears as a white to off-white crystalline solid. Its crystalline form aids in easy identification and handling in laboratory settings.

Comment on solubility

Solubility of N-(3-chloro-4-cyano-phenyl)acetamide

N-(3-chloro-4-cyano-phenyl)acetamide exhibits a unique solubility profile influenced by its molecular structure. This compound can be characterized by the following solubility characteristics:

  • The presence of the chloro and cyano groups tends to increase polarity, which may enhance its solubility in polar solvents.
  • It is generally expected to be soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF).
  • However, its solubility in water is likely to be limited due to its overall hydrophobic characteristics.

In practical terms, understanding the solubility of this compound is essential for applications in fields such as pharmaceuticals and materials science, as it influences factors such as bioavailability and reaction kinetics. As quoted from solubility studies, "the solubility of a compound dictates not only its usability but also its effectiveness in various reactions."

Overall, the solubility of N-(3-chloro-4-cyano-phenyl)acetamide can be best assessed through experimental measurements, particularly in the context of its intended application.

Interesting facts

Interesting Facts About N-(3-chloro-4-cyano-phenyl)acetamide

N-(3-chloro-4-cyano-phenyl)acetamide is a fascinating compound that plays significant roles in various fields of chemistry and pharmaceuticals. Here are some key points to consider:

  • Pharmaceutical Importance: This compound is often studied for its potential in drug development, particularly in the arena of anti-cancer therapies. Researchers are exploring its effects on tumor growth inhibition.
  • Synthetic Versatility: It's valued for its versatility in organic synthesis, where it can serve as an intermediate in producing other important chemical compounds.
  • Functional Groups: The presence of a cyano group (-C≡N) enhances its reactivity and presents intriguing pathways for chemical modification.
  • Structure-Activity Relationship (SAR): The positioning of the chloro and cyano groups plays a crucial role in determining the biological activity of the molecule, making it a focal point for structure-activity studies.
  • Research Implications: Studies on this compound contribute to our understanding of molecular interactions, which can lead to better therapeutic agents with fewer side effects.

As a compound with unique characteristics, N-(3-chloro-4-cyano-phenyl)acetamide is more than just a simple organic molecule; it embodies the heart of **chemical innovation** and **biological exploration**.

In summary, this compound showcases the intricate relationship between molecular structure and function, making it a subject of ongoing research and discovery in the scientific community.

Synonyms
22304-33-2
2-CHLORO-4-ACETYLAMINOBENZONITRILE
BW 63-307
Acetamide, N-(3-chloro-4-cyanophenyl)-
BW-63-307
E5RR46DF69
DTXSID30176848
RefChem:122412
DTXCID3099339
N-(3-chloro-4-cyanophenyl)acetamide
Oprea1_722108
Acetamide,N-(3-chloro-4-cyanophenyl)-
SCHEMBL16728601
Acetanilide, 3'-chloro-4'-cyano-
STL260218
AKOS002376690
ST50486246
AS-871/14925059