Skip to main content

9-Vinylcarbazole

ADVERTISEMENT
Identification
Molecular formula
C14H11N
CAS number
1484-13-5
IUPAC name
9-vinylcarbazole
State
State

At room temperature, 9-vinylcarbazole is a solid. Its crystalline structure contributes to its stability and photoconductive properties.

Melting point (Celsius)
67.00
Melting point (Kelvin)
340.15
Boiling point (Celsius)
196.00
Boiling point (Kelvin)
469.15
General information
Molecular weight
219.29g/mol
Molar mass
219.2860g/mol
Density
1.0897g/cm3
Appearence

9-Vinylcarbazole appears as a light yellow crystalline solid. It is granular in texture and can also be found as a powder. The compound is known for its photoreactive properties.

Comment on solubility

Solubility of 9-vinylcarbazole

9-vinylcarbazole is a fascinating compound that exhibits unique solubility characteristics. Here are some key points about its solubility:

  • Solvent Compatibility: 9-vinylcarbazole is soluble in organic solvents such as tetrahydrofuran (THF), chloroform, and dimethyl sulfoxide (DMSO). This enables it to be utilized in various organic reactions and processes.
  • Polarity Impact: Its solubility can be largely attributed to the compound's non-polar nature, allowing it to dissolve well in non-polar and slightly polar solvents.
  • Limited Aqueous Solubility: Unfortunately, 9-vinylcarbazole exhibits very low solubility in water, making it less suitable for aqueous applications. This aligns with the general behavior of organic compounds that are large and aromatic.
  • Application Considerations: The solubility profile influences its applications, especially in fields such as polymer science and organic electronics. The choice of solvent can be critical for successfully utilizing this compound.

In summary, while 9-vinylcarbazole is versatile in organic solvents, its overall solubility in water is limited, which shapes its practical applications distinctly.

Interesting facts

Interesting Facts about 9-Vinylcarbazole

9-Vinylcarbazole is a fascinating compound that combines the properties of vinyl and carbazole moieties, making it significant in various chemical applications. Here are some key insights about this unique compound:

  • Structure and Reactivity: 9-Vinylcarbazole contains both an aromatic ring and a vinyl group, which lends it a degree of reactivity that is useful in polymer chemistry.
  • Polymerization Potential: This compound is known for its ability to undergo free radical polymerization, which is valuable for creating specialty polymers and plastic materials.
  • Applications in Electronics: Due to its conductive properties, 9-vinylcarbazole is often utilized in the field of organic electronics, particularly in the manufacture of light-emitting diodes (LEDs) and photovoltaic cells.
  • Photochemical Uses: The compound is sensitive to light, providing opportunities for photochemical reactions that can lead to innovative solutions in materials science and organic synthesis.
  • Historical Context: Discovered in the mid-20th century, 9-vinylcarbazole has since gained attention not only for its chemical versatility but also for its role in advancing the field of organic semiconductors.

As a compound, 9-vinylcarbazole exemplifies the intersection of organic chemistry and material science. It serves as a bridge for developing new technologies, particularly in electronic devices where lightweight and flexible materials are paramount. Its remarkable properties continue to inspire research and innovation in emerging fields!

Synonyms
9-Vinylcarbazole
1484-13-5
N-Vinylcarbazole
9-Vinyl-9H-carbazole
9H-Carbazole, 9-ethenyl-
Vinylcarbazole
1-Vinylcarbazole
9-Ethenyl-9H-carbazole
CARBAZOLE, 9-VINYL-
N-Ethenylcarbazole
N-Vinylkarbazol
N-Vinylkarbazol [Czech]
EINECS 216-055-0
NSC 406868
BRN 0132988
D629AMY6F9
AI3-08510
VINYLCARBAZOLE, N-
NSC-406868
DTXSID4022155
5-20-08-00019 (Beilstein Handbook Reference)
DTXCID902155
216-055-0
N-Vinyl carbazole
9-ethenylcarbazole
UNII-D629AMY6F9
9-vinyl carbazole
MFCD00004966
MFCD00134336
9-Vinylcarbazole, 98%
9-Vinyl-9H-carbazole #
SCHEMBL36244
KKFHAJHLJHVUDM-UHFFFAOYSA-
BCP32572
NSC406868
AKOS003654048
CS-W010679
FV06367
N-Vinylcarbazole;9-Vinyl-9H-carbazole
AS-14834
DB-042935
NS00024857
V0021
EN300-20171
G67520
A808764
Q3334160
InChI=1/C14H11N/c1-2-15-13-9-5-3-7-11(13)12-8-4-6-10-14(12)15/h2-10H,1H2