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Dimethylphenylacetamide

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Identification
Molecular formula
C12H17NO2
CAS number
93-02-7
IUPAC name
N-[2-(dimethylamino)-2-oxo-ethyl]-2-phenyl-acetamide
State
State

At room temperature, Dimethylphenylacetamide is typically in a liquid state. This compound remains in liquid form under normal atmospheric pressure and standard conditions due to its relatively low melting point.

Melting point (Celsius)
32.00
Melting point (Kelvin)
305.15
Boiling point (Celsius)
289.00
Boiling point (Kelvin)
562.15
General information
Molecular weight
193.25g/mol
Molar mass
193.2460g/mol
Density
1.0845g/cm3
Appearence

Dimethylphenylacetamide appears as a colorless to light yellow liquid. It is typically clear and has a characteristic amide odor. As a chemical used in various industrial applications, its appearance may vary slightly depending on specific impurities or formulations.

Comment on solubility

Solubility of N-[2-(dimethylamino)-2-oxo-ethyl]-2-phenyl-acetamide

N-[2-(dimethylamino)-2-oxo-ethyl]-2-phenyl-acetamide exhibits intriguing solubility characteristics, often influenced by its molecular structure. This compound is notable for:

  • Polar Functional Groups: The presence of the dimethylamino group enhances its polarity, potentially leading to increased solubility in polar solvents such as water or alcohols.
  • Hydrophobic Phenyl Ring: However, the phenyl group contributes to hydrophobicity, which might reduce its overall solubility in strictly polar solvents.
  • SOLVENT INTERACTIONS: The solubility can vary significantly with different solvents, and it is often soluble in organic solvents like dichloromethane or ethanol.

As a general rule, the solubility of such compounds can be summarized by the phrase: "like dissolves like." Thus, understanding the balance between polar and non-polar characteristics provides crucial insights into its solubility behavior. This dual nature underscores the importance of solvent choice for achieving optimal dissolution properties.

Interesting facts

Interesting Facts about N-[2-(dimethylamino)-2-oxo-ethyl]-2-phenyl-acetamide

N-[2-(dimethylamino)-2-oxo-ethyl]-2-phenyl-acetamide is a fascinating compound with a variety of intriguing properties and applications. Here are some key points to consider:

  • Pharmacological Significance: This compound is often studied in the context of medicinal chemistry due to its potential as a pharmaceutical agent. Its structure suggests roles in various therapeutic areas, including analgesic and anti-inflammatory treatments.
  • Structure-Activity Relationship: The presence of a dimethylamino group contributes significantly to the compound's biological activity. Such functional groups can enhance lipophilicity, potentially improving the absorption and efficacy of the compound in biological systems.
  • Research Applications: Scientists have explored the efficacy of this compound in drug development, especially for targeting specific receptors or enzymes involved in disease mechanisms. Its unique structural features make it a candidate for further exploration in synthetic organic chemistry.
  • Mechanism of Action: Its mechanism of action may involve altering neurotransmitter levels or inhibiting specific enzymes, which are critical in various metabolic pathways. Understanding these mechanisms opens up avenues for novel treatments.
  • Synthesis Challenges: The synthesis of N-[2-(dimethylamino)-2-oxo-ethyl]-2-phenyl-acetamide can pose challenges due to the need for precise conditions to favor the formation of the desired compound over side products.

As you delve into the studies of N-[2-(dimethylamino)-2-oxo-ethyl]-2-phenyl-acetamide, remember: “The journey of discovery in chemistry requires both patience and curiosity.” This compound symbolizes the intersection of theoretical knowledge and practical application in the field of science.


Synonyms
N,N-Dimethyl-2-(2-phenylacetamido)acetamide
25439-20-7
83K5TKJ4WW
DTXSID9048851
DTXCID2028777
RefChem:1090520
NCGC00181910-01
BRN 2458870
UNII-83K5TKJ4WW
ACETAMIDE, N,N-DIMETHYL-2-(2-PHENYLACETAMIDO)-
Tox21_113335
AKOS030583218
CAS-25439-20-7
Q27269440
Z32015017