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Bis(1-naphthyl) carbonate

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Identification
Molecular formula
C21H14O3
CAS number
1082-03-9
IUPAC name
bis(1-naphthyl) carbonate
State
State

At room temperature, bis(1-naphthyl) carbonate is a solid. It retains its solid form under normal storage conditions and should be handled in a way that minimizes dust generation.

Melting point (Celsius)
149.00
Melting point (Kelvin)
422.20
Boiling point (Celsius)
462.50
Boiling point (Kelvin)
735.70
General information
Molecular weight
326.34g/mol
Molar mass
326.3380g/mol
Density
1.3030g/cm3
Appearence

Bis(1-naphthyl) carbonate appears as a white to slightly off-white crystalline solid. It has a characteristic aromatic odor due to the naphthyl groups.

Comment on solubility

Solubility of Bis(1-naphthyl) carbonate

Bis(1-naphthyl) carbonate, with the chemical formula C18H14O3, exhibits intriguing solubility characteristics that are worth noting. This compound is categorized as an organic carbonate, which often influences its ability to dissolve in various solvents.

Here are some key points regarding its solubility:

  • Polar solvents: Bis(1-naphthyl) carbonate generally shows limited solubility in polar solvents due to its non-polar hydrocarbon backbone.
  • Non-polar solvents: It tends to dissolve well in non-polar organic solvents, such as hexane and benzene, which favor hydrophobic interactions.
  • Temperature Effects: Solubility may increase with elevated temperatures, as is common with many organic compounds.
  • Applications: Understanding its solubility is crucial for applications in organic synthesis and materials science.

In summary, while bis(1-naphthyl) carbonate is not highly soluble in polar environments, it demonstrates a predisposition for dissolution in non-polar solvents, making its behavior predictable in organic chemistry settings.

Interesting facts

Interesting Facts About Bis(1-naphthyl) Carbonate

Bis(1-naphthyl) carbonate is an intriguing compound with numerous fascinating aspects worth exploring. This compound, which belongs to the class of organic carbonates, showcases unique chemical behavior and applications. Here are some interesting highlights:

  • Structure and Formation: Bis(1-naphthyl) carbonate consists of two 1-naphthyl groups esterified with a carbonate functional group. This structure contributes to its unique physical and chemical properties.
  • Polymer Applications: This compound is significant in the realm of polymer chemistry, often utilized as a monomer in the production of polycarbonate materials. Such polymers are renowned for their strength and transparency, making them valuable in various industries from automotive to electronics.
  • Photochemical Properties: Bis(1-naphthyl) carbonate exhibits interesting photochemical behavior, which assists in photochemical polymerization processes. This reactivity in UV-light exposure enables the development of innovative coatings and adhesives.
  • Biological Significance: Some studies suggest that derivatives of bis(1-naphthyl) carbonate may possess biologically relevant properties, including potential anti-proliferative effects on certain cancer cells. This avenue of research opens doors to new therapeutic applications.
  • Environmental Impact: The biodegradability of carbonates, including bis(1-naphthyl) carbonate, has drawn attention to their potential as environmentally friendly alternatives in various applications, reducing reliance on more hazardous compounds.

In the words of renowned chemist John McMurry, "Chemistry is a remarkable science that reveals the underlying beauty of the world." Bis(1-naphthyl) carbonate exemplifies this idea, combining elegance in its molecular architecture with practical applications in daily life.

With ongoing research into its properties and new applications emerging, bis(1-naphthyl) carbonate continues to be a compound of interest for chemists and scientists alike.

Synonyms
Di-1-naphthyl carbonate
Bis(1-naphthyl)carbonate
Di-alpha-naphthyl carbonate
3159-41-9
1-Naphthalenol, carbonate (2:1)
CARBONIC ACID, BIS(1-NAPHTHYL) ESTER
ZGD36Y4MUJ
NSC-47202
dinaphthalen-1-yl carbonate
Carbonic acid, di-1-naphthyl ester
NSC 47202
BRN 2152199
dinaphthylcarbonat
UNII-ZGD36Y4MUJ
di(1-naphthyl) carbonate
SCHEMBL37865
0-06-00-00609 (Beilstein Handbook Reference)
DTXSID70953554
NSC47202
AKOS024330912