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2-(Diethylamino)naphthalene-1,4-dione

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Identification
Molecular formula
C14H15NO2
CAS number
3375-24-0
IUPAC name
2-(diethylamino)naphthalene-1,4-dione
State
State
At room temperature, this compound is generally in a solid state. It is typically stored as a powder or crystalline substance in laboratory settings.
Melting point (Celsius)
78.00
Melting point (Kelvin)
351.00
Boiling point (Celsius)
465.00
Boiling point (Kelvin)
738.00
General information
Molecular weight
241.28g/mol
Molar mass
242.3010g/mol
Density
1.2540g/cm3
Appearence

The compound 2-(Diethylamino)naphthalene-1,4-dione appears as a solid with a distinctive crystalline structure. It is typically light yellow or orange in color, depending on purity and form.

Comment on solubility

Solubility of 2-(diethylamino)naphthalene-1,4-dione

The solubility of 2-(diethylamino)naphthalene-1,4-dione can be quite intriguing due to its unique molecular structure and the presence of functional groups. Here are some key points to consider:

  • Solvent Polarities: The solubility of this compound is influenced by solvent polarity. It is generally soluble in organic solvents such as ethanol, acetone, and chloroform due to its non-polar aromatic ring.
  • Temperature Factors: Solubility may increase with temperature. As with many organic compounds, heating can enhance the dissolution process.
  • pH Impact: The solubility in aqueous solutions can be affected by pH. The presence of the -NH group in the diethylamino moiety may cause it to behave differently under various pH conditions.
  • Complexation Possibilities: This compound can form complexes with other molecules, which can alter its solubility profile significantly.

In conclusion, the solubility of 2-(diethylamino)naphthalene-1,4-dione is versatile, but understanding its behavior in different environments is key to leveraging its potential. As stated, "The right solvent can make all the difference!"

Interesting facts

Interesting Facts about 2-(Diethylamino)naphthalene-1,4-dione

2-(Diethylamino)naphthalene-1,4-dione, often referred to as a derivative of naphthoquinone, has captured the attention of scientists due to its fascinating properties and applications. Here are some highlights:

  • Diverse Applications: This compound is primarily utilized in the fields of organic synthesis and photochemistry. Its unique structure allows for various reactions that can lead to the production of more complex molecules.
  • Fluorescence: 2-(Diethylamino)naphthalene-1,4-dione exhibits **fluorescent** properties, making it an interesting candidate for use in *fluorescent probes* and **dye sensitized solar cells**.
  • Biological Interest: The compound's derivatives have been studied for their potential *antioxidant* activities, which could have implications in biomedical research. Some compounds in this family show promise in **pharmaceutical development**.
  • Reactivity: It participates in various **redox reactions**, which can be useful in studying reaction mechanisms or developing new reaction protocols in organic chemistry.
  • Research Insights: Scientists have shown a keen interest in understanding the *photo-physical* properties of this compound, as they can lead to advancements in *optical materials* and *light-harvesting systems*.

As the field of chemistry continues to evolve, compounds like 2-(diethylamino)naphthalene-1,4-dione remind us of the intricate relationships between structure, reactivity, and application. Consequently, they represent a rich area of study for both researchers and students alike. In the words of a renowned chemist, "Understanding these compounds helps us pave the way for innovative solutions in science."

Synonyms
2-Diethylamino-1,4-naphthoquinone
1,4-NAPHTHOQUINONE, 2-DIETHYLAMINO-
1,4-Naphthalenedione, 2-(diethylamino)-
14422-78-7
ZQS7YYP57L
NSC-222690
NSC 222690
2-(diethylamino)naphthalene-1,4-dione
BRN 2723745
NSC222690
1, 2-diethylamino-
UNII-ZQS7YYP57L
diethylamino naphthoquinone
1, 2-(diethylamino)-
SCHEMBL7516711
DTXSID60162653
YWEDSYCFWBEXBJ-UHFFFAOYSA-N
WLN: L66 BV EVJ CN2&2
2-(DIETHYLAMINO)-1,4-NAPHTHALENEDIONE