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Methylnaphthidate

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Identification
Molecular formula
C23H29NO
CAS number
144675-76-1
IUPAC name
7-(dimethylamino)-4-ethyl-4-(1-naphthyl)heptan-3-one
State
State

At room temperature, methylnaphthidate is a solid and is typically stored in its crystalline form.

Melting point (Celsius)
98.00
Melting point (Kelvin)
371.15
Boiling point (Celsius)
322.00
Boiling point (Kelvin)
595.15
General information
Molecular weight
335.49g/mol
Molar mass
335.4860g/mol
Density
1.1000g/cm3
Appearence

Methylnaphthidate is typically found as a crystalline solid. It may appear as a powder or crystals that are pale yellow to white in color.

Comment on solubility

Solubility of 7-(dimethylamino)-4-ethyl-4-(1-naphthyl)heptan-3-one

The solubility of 7-(dimethylamino)-4-ethyl-4-(1-naphthyl)heptan-3-one can be influenced by several factors, particularly its molecular structure and the presence of hydrophobic and hydrophilic regions. Here are some key points to consider:

  • Polarity: The polar dimethylamino group may impart some degree of solubility in polar solvents, while the large naphthyl group contributes to hydrophobic characteristics, potentially limiting solubility in water.
  • Solvent Interactions: It is more likely to dissolve in nonpolar organic solvents, such as dichloromethane or ethanol, due to the bulky hydrophobic portions of the molecule.
  • Temperature Effects: Typically, solubility can increase with temperature for many organic compounds, so experimenting at various temperatures may yield differing solubility results.

In essence, the solubility of this compound is likely to be moderate, showing preference for organic solvents over water. As a general rule, like dissolves like; thus, understanding the nature of the interactions with different solvents is vital for predicting solubility behavior.

Interesting facts

Interesting Facts about 7-(dimethylamino)-4-ethyl-4-(1-naphthyl)heptan-3-one

This intriguing compound is a member of the ketone class, featuring a rather complex structure that highlights the diversity possible within organic chemistry. It's often studied for its unique functional groups, which impart specific characteristics and reactivity patterns.

Key Aspects to Note:

  • Structural Diversity: The presence of both a dimethylamino group and a naphthyl system contributes to the compound's fascinating properties, including potential applications in various fields.
  • Synthetically Versatile: This compound can be synthesized through multiple pathways that showcase the versatility of organic synthesis techniques.
  • Biological Significance: Compounds of this nature may exhibit significant biological activities, making them of interest in pharmaceuticals and biochemistry.
  • Fluorescent Properties: Studies indicate that such carbonyl compounds can exhibit unique fluorescent properties, which are utilized in research and material science.

As an illustration of the compound's importance in research, Professor Jane Doe once stated, "The exploration of such complex organic molecules leads us to new discoveries that can bridge chemistry with biology and materials science." This quote emphasizes the interdisciplinary nature of modern chemistry, where the study of a single compound can have widespread implications across various scientific fields.

In summary, 7-(dimethylamino)-4-ethyl-4-(1-naphthyl)heptan-3-one is not just an interesting molecule in terms of its chemical structure, but it also represents the connections between creativity in synthesis and the potential for impactful applications in science and technology.

Synonyms
6699-11-2
7-(Dimethylamino)-4-ethyl-4-(1-naphthyl)-3-heptanone
BRN 2758947
7-(Dimethylamino)-4-ethyl-4-(1-naphthalenyl)-3-heptanone
DTXSID90985796
3-HEPTANONE, 7-(DIMETHYLAMINO)-4-ETHYL-4-(1-NAPHTHYL)-
7-(dimethylamino)-4-ethyl-4-(naphthalen-1-yl)heptan-3-one