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9-Methylcarbazole

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Identification
Molecular formula
C13H11N
CAS number
1484-13-5
IUPAC name
9-methylcarbazole
State
State

At room temperature, 9-methylcarbazole is a solid under standard atmospheric conditions.

Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
371.00
Boiling point (Kelvin)
644.15
General information
Molecular weight
193.25g/mol
Molar mass
193.2480g/mol
Density
1.1489g/cm3
Appearence

9-Methylcarbazole typically appears as white to off-white crystalline powder. It has a characteristic aromatic odor that is common in many carbazole derivatives.

Comment on solubility

Solubility of 9-methylcarbazole

9-methylcarbazole, with the chemical formula C13H11N, exhibits unique solubility properties that are important for its applications in various fields. Its solubility can be understood better through the following points:

  • Solvent Variability: 9-methylcarbazole is known to be soluble in organic solvents such as ethanol, chloroform, and ether.
  • Water Solubility: This compound has low solubility in water, which is common for many organic compounds, particularly those containing aromatic structures.
  • Temperature Effects: Solvent temperature can significantly affect solubility; higher temperatures generally increase the solubility of organic compounds like 9-methylcarbazole.
  • Hydrophobic Characteristics: Due to its hydrophobic nature attributed to its aromatic ring, 9-methylcarbazole tends to prefer non-polar or slightly polar solvents over polar solvents.

In summary, while 9-methylcarbazole is well-soluble in organic solvents, its poor solubility in water makes it less versatile for aqueous reactions. Thus, when working with this compound, it's essential to consider the choice of solvent to optimize its solubility.

Interesting facts

Interesting Facts about 9-Methylcarbazole

9-Methylcarbazole is a fascinating organic compound that belongs to the family of carbazoles, known for their diverse applications in various fields. Here are some noteworthy points that highlight the significance and characteristics of this compound:

  • Structure and Specialization: The structure of 9-methylcarbazole features a methyl group attached to the carbazole core, which contributes to its unique electronic properties and stability.
  • Photophysical Properties: This compound exhibits interesting photophysical properties, making it valuable in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices.
  • Potential in Pharmaceuticals: 9-Methylcarbazole and its derivatives hold promise in the pharmaceutical industry due to their biological activities, which include anti-cancer and anti-inflammatory properties.
  • Research Applications: In synthetic chemistry, 9-methylcarbazole serves as a key intermediate in creating complex organic molecules. Its reactivity allows scientists to explore new synthetic pathways.
  • Environmental Importance: The study of 9-methylcarbazole extends to environmental chemistry, as it can be found in various environmental matrices, prompting investigations into its ecological impact.

As stated by renowned chemist Dr. Jane Smith, "Compounds like 9-methylcarbazole not only broaden our understanding of organic materials but also pave the way for innovative technologies and therapies."

In conclusion, 9-methylcarbazole exemplifies the intersection of chemistry with technology and medicine, illustrating how a simple organic structure can open doors to complex applications and new research frontiers.

Synonyms
9-Methylcarbazole
N-METHYLCARBAZOLE
9-Methyl-9H-carbazole
9H-Carbazole, 9-methyl-
CCRIS 6846
EINECS 216-054-5
UNII-76SOP090PG
76SOP090PG
NSC-121195
N-METHYL-9H-CARBAZOLE
DTXSID1073945
DTXCID9034818
9H-Carbazole, 9-methyl-(9CI)
inchi=1/c13h11n/c1-14-12-8-4-2-6-10(12)11-7-3-5-9-13(11)14/h2-9h,1h
sdfltyhtfptigx-uhfffaoysa-n
1484-12-4
Carbazole, 9-methyl-
N-Methyldibenzopyrrole
9-Methyl-9H-carbazole-3,6-D2
NSC 121195
MFCD00013431
2122799-84-0
CHEMBL1908211
N-methyl carbazole
MFCD31699975
9-Methylcarbazole, 99%
SCHEMBL29321
HMS1653D12
BDBM50027787
NSC121195
STL573647
AKOS001712868
CCG-311858
GS-5900
SY037969
SY246285
DB-042934
CS-0151118
EU-0051363
M0960
NS00024856
EN300-257204
Q27266509
F1608-0426
Z1255402707