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DMAPN

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Identification
Molecular formula
C25H31NO2
CAS number
54932-56-4
IUPAC name
phenyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate
State
State
DMAPN is generally found as a solid at room temperature, typically in a crystalline form.
Melting point (Celsius)
90.00
Melting point (Kelvin)
363.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
353.50g/mol
Molar mass
353.4970g/mol
Density
1.0200g/cm3
Appearence

DMAPN typically appears as a white crystalline powder.

Comment on solubility

Solubility of Phenyl 5-(Dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate

When exploring the solubility of phenyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate, we can make some insightful observations:

  • Solvent Compatibility: This compound displays varied solubility behaviors depending on the solvent used. It tends to have better solubility in organic solvents such as ethanol and methanol.
  • Polarity Considerations: Being a larger organic molecule with non-polar naphthalene groups, the compound is likely to be less soluble in polar solvents like water.
  • Effects of Substituents: The presence of the dimethylamino group can enhance solubility in some organic solvents due to its ability to interact through hydrogen bonding.
  • Temperature Influence: Generally, solubility can increase with temperature. Conducting experiments at various temperatures might yield more favorable results.

As a general rule, like dissolves like: polar compounds tend to dissolve in polar solvents, while non-polar compounds favor non-polar solvents. Therefore, understanding the specific characteristics of the surrounding environment is crucial when predicting solubility for phenyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate.

Interesting facts

Interesting Facts about Phenyl 5-(Dimethylamino)-2-Isopropyl-2-(1-Naphthyl)pentanoate

Pursuing the complexities of chemical compounds can often lead to the discovery of fascinating insights and applications. One such compound, phenyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate, is a notable entity in the field of organic chemistry.

Structural Characteristics

This compound exhibits a unique structure characterized by:

  • Phenyl Group: The presence of a phenyl group contributes to the compound’s hydrophobic properties, making it an intriguing candidate for various applications.
  • Dimethylamino Group: The dimethylamino group confers basicity, allowing potential interactions in biological systems.
  • Naphthyl Substituent: The naphthyl part adds aromatic character, influencing the compound's reactivity and stability.

Biological Relevance

This compound is of particular interest due to its potential applications in pharmacology. Here are some areas where it might play a role:

  • Pharmaceutical Development: The unique structure may contribute to the development of novel therapeutics.
  • Research in Neuroscience: The dimethylamino group suggests a possible activity related to neurotransmission, making it a subject of interest in studies of psychotropic compounds.
  • Drug Design: The compound can serve as a lead structure or motif in designing new drugs targeting specific biological pathways.

Conclusion

In summary, phenyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate stands out not only for its interesting synthetic attributes but also for its potential contributions to various scientific fields. As research into organic compounds continues to evolve, this compound may well unlock new avenues in both understanding and application.

Synonyms
6779-74-4
BRN 2782594
alpha-(3-(Dimethylamino)propyl)-alpha-isopropyl-1-naphthaleneacetic acid phenyl ester
1-Naphthaleneacetic acid, alpha-(3-(dimethylamino)propyl)-alpha-isopropyl-, phenyl ester
DTXSID40987124
Phenyl 5-(dimethylamino)-2-(naphthalen-1-yl)-2-(propan-2-yl)pentanoate