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Tetrahydrocarbazole

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Identification
Molecular formula
C12H13N
CAS number
942-01-8
IUPAC name
2,3,4,9-tetrahydro-1H-carbazole
State
State

Tetrahydrocarbazole is a solid at room temperature.

Melting point (Celsius)
113.40
Melting point (Kelvin)
386.60
Boiling point (Celsius)
313.00
Boiling point (Kelvin)
586.00
General information
Molecular weight
171.25g/mol
Molar mass
171.2480g/mol
Density
1.1570g/cm3
Appearence

Tetrahydrocarbazole presents as a colorless to pale yellow solid. It may appear crystalline depending on the method of preparation and conditions of storage.

Comment on solubility

Solubility of 2,3,4,9-tetrahydro-1H-carbazole

2,3,4,9-tetrahydro-1H-carbazole, a heterocyclic compound, presents interesting solubility characteristics. Its solubility can be described using the following key points:

  • Polar vs. Non-Polar Solvents: This compound is expected to be more soluble in non-polar solvents due to its hydrophobic nature. Organic solvents such as benzene or diethyl ether are likely to support better solubility.
  • Water Solubility: In contrast, its solubility in water is limited. This is primarily due to the low polarity of the compound, which does not interact favorably with the polar water molecules.
  • Temperature Influence: As with many organic compounds, solubility can vary with temperature; an increase in temperature usually enhances solubility in organic solvents.
  • Impurities and Crystal Structure: The presence of impurities and the crystal structure can significantly affect solubility, illustrating the complexity of dissolution processes.

Overall, the solubility of 2,3,4,9-tetrahydro-1H-carbazole is predominantly dictated by its non-polar characteristics, making it suitable for applications where organic solvents are utilized. Understanding these solubility properties can be essential for its use in various chemical reactions and formulations.

Interesting facts

Interesting Facts About 2,3,4,9-Tetrahydro-1H-Carbazole

2,3,4,9-Tetrahydro-1H-carbazole is a fascinating nitrogen-containing heterocyclic compound known for its diverse applications and intriguing structure. Here are some interesting facts:

  • Structural Uniqueness: This compound features a bicyclic structure that combines a carbazole framework with additional hydrogen atoms, enhancing its stability and reactivity. The presence of multiple rings contributes to its complex chemistry.
  • Biological Importance: 2,3,4,9-Tetrahydro-1H-carbazole and its derivatives have garnered attention in medicinal chemistry for their potential pharmacological properties, including anti-cancer and neuroprotective effects. They may inhibit certain enzymes, thereby impacting cell signaling pathways.
  • Materials Science: This compound is explored in the field of materials science, specifically for its potential use in organic electronic devices and sensors. The conjugated system provides interesting electronic properties that can be harnessed in various applications.
  • Research Interest: Scientists are intrigued by the synthetic methodologies developed to create this compound. Complex synthesis routes often involve multi-step reactions, which are a testament to the versatility of organic synthesis techniques.
  • Derivatives and Variants: The study of 2,3,4,9-tetrahydro-1H-carbazole has led to the discovery of numerous analogs and derivatives, each exhibiting unique properties and potential applications in different chemical contexts.

In summary, 2,3,4,9-tetrahydro-1H-carbazole represents a compound that is not only central to various scientific explorations but also serves as a bridge between organic synthesis and applications in health and technology. As you delve deeper into its chemistry, you may find that its potential is just beginning to be fully appreciated.

Synonyms
1,2,3,4-Tetrahydrocarbazole
2,3,4,9-Tetrahydro-1H-carbazole
942-01-8
5,6,7,8-Tetrahydrocarbazole
1H-Indole, 2,3-(1,4-butanediyl)-
CARBAZOLE, 5,6,7,8-TETRAHYDRO-
NSC 17329
UNII-8ZLK0TSX93
EINECS 213-385-7
8ZLK0TSX93
BRN 0133771
5,6,7,8-Tetrahydro-9H-carbazole
NSC-17329
DTXSID00240969
5-20-07-00468 (Beilstein Handbook Reference)
CARBAZOLE,1,2,3,4-TETRAHYDRO
2,3,4,9-TETRAHYDRO-9H-CARBAZOLE
2,3Tetramethyleneindole
2,3Tetramethylene1Hindole
5,6,7,8Tetrahydrocarbazole
2,3,4,9Tetrahydro1Hcarbazole
Carbazole, 1,2,3,4tetrahydro
Carbazole, 5,6,7,8tetrahydro
DTXCID80163460
1HIndole, 2,3(1,4butanediyl)
1HCarbazole, 2,3,4,9tetrahydro
1234-THC
Carbazole, 1,2,3,4tetrahydro (8CI)
1HCarbazole, 2,3,4,9tetrahydro (9CI)
inchi=1/c12h13n/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1,3,5,7,13h,2,4,6,8h
xklnovwdvmwtob-uhfffaoysa-n
Tetrahydrocarbazole
2,3-Tetramethyleneindole
2,3-Tetramethylene-1H-indole
1H-Carbazole, 2,3,4,9-tetrahydro-
Carbazole, 1,2,3,4-tetrahydro-
MFCD00004959
tetrahydocarbazole
1,2,3,4,-TETRAHYDROCARBAZOLE
1,3,4-Tetrahydrocarbazole
5,7,8-Tetrahydrocarbazole
SCHEMBL104598
1.2.3.4-Tetrahydrocarbazole
Carbazole,2,3,4-tetrahydro-
Carbazole,6,7,8-tetrahydro-
CHEMBL1911317
WLN: T B656 HM&&TJ
HMS1651H10
1H-Carbazole,3,4,9-tetrahydro-
1,2,3,4-tetrahydro-9H-carbazole
1H-Indole,3-(1,4-butanediyl)-
ALBB-017903
NSC17329
STK394140
1,2,3,4-Tetrahydrocarbazole, 99%
AKOS000271191
2,3,4,9-Tetrahydro-1H-carbazole #
CS-W004910
NCGC00186306-01
AC-11745
SY033427
DB-057479
EU-0070508
NS00040254
T1006
EN300-82532
AB-337/25021010
AH-034/32847041
SR-01000424125
SR-01000424125-1
Q27271250
F0832-0099
F1918-0039