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N-(4-chlorophenyl)-2-fluoroacetamide

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Identification
Molecular formula
C8H7ClFNO
CAS number
28485-88-7
IUPAC name
N-(4-chlorophenyl)-2-fluoro-acetamide
State
State
At room temperature, N-(4-chlorophenyl)-2-fluoroacetamide is in a solid state. Its crystalline form is stable and it remains solid under standard temperature and pressure conditions.
Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
315.80
Boiling point (Kelvin)
588.95
General information
Molecular weight
187.59g/mol
Molar mass
187.5880g/mol
Density
1.4412g/cm3
Appearence

N-(4-chlorophenyl)-2-fluoroacetamide is typically in a crystalline solid form. The appearance can be white to off-white, depending on purity and specific synthetic route undertaken during its preparation.

Comment on solubility

Solubility of N-(4-chlorophenyl)-2-fluoro-acetamide

N-(4-chlorophenyl)-2-fluoro-acetamide, a compound notable for its distinct functional groups, exhibits interesting solubility characteristics. Understanding the solubility of this compound is essential for its applications, especially in pharmaceuticals and chemical synthesis. Here are some key points regarding its solubility:

  • Polarity: The presence of the 4-chlorophenyl and 2-fluoro groups contributes to a moderately polar nature, which typically influences solubility in various solvents.
  • Solvent Affinity: N-(4-chlorophenyl)-2-fluoro-acetamide is more soluble in polar solvents such as water and ethanol, compared to non-polar solvents.
  • Hydrogen Bonding: The amide functional group can engage in hydrogen bonding, enhancing its solubility in polar mediums.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, potentially aiding in its dissolution.

It's crucial to note that while the compound may demonstrate a reasonable degree of solubility, factors such as concentration and temperature play a significant role in its solubility behavior. Additionally, compatibility with various solvents can significantly influence how it behaves in different chemical environments. Consequently, while working with N-(4-chlorophenyl)-2-fluoro-acetamide, one should evaluate the solvent system carefully to optimize its use in applications.

Interesting facts

Interesting Facts about N-(4-chlorophenyl)-2-fluoro-acetamide

N-(4-chlorophenyl)-2-fluoro-acetamide, often abbreviated as CFPA, is a fascinating compound that has garnered attention in the fields of pharmaceuticals and organic synthesis. Here are some notable aspects of this compound:

  • Pharmaceutical Significance: CFPA serves as an important intermediate in the synthesis of various drugs, particularly in the search for effective treatments for ailments such as cancer and bacterial infections.
  • Structure-Activity Relationship: The presence of both the chlorophenyl and fluoro substituents greatly influences the biological activity of the compound. This leads researchers to study how modifications affect therapeutic efficacy.
  • Fluorine's Role: The fluorine atom contributes to increased lipophilicity, which can facilitate better membrane permeability—an essential factor in drug design.
  • Synthetic Pathways: The synthesis of CFPA often involves strategic reactions such as nucleophilic acyl substitution, which illustrates the elegance and complexity of organic chemistry.
  • Applications Beyond Medicine: Beyond its pharmaceutical applications, CFPA is also used in materials science, where it can play a role in developing new polymers and other functional materials.

In conclusion, N-(4-chlorophenyl)-2-fluoro-acetamide is not just another compound; its unique structural features and varied applications make it a subject of great interest in modern chemistry. As researchers continue to explore its potential, CFPA remains a prime example of how chemical compounds can have far-reaching implications across multiple scientific disciplines.

Synonyms
N-(4-chlorophenyl)-2-fluoroacetamide
404-41-1
p-Chlorofluoroacetanilide
ACETANILIDE, 4'-CHLORO-2-FLUORO-
4'-Chloro-2-fluoroacetanilide
BRN 2803933
DTXSID00193401
4-12-00-01179 (Beilstein Handbook Reference)
SCHEMBL8876305
DTXCID70115892