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Ellipticine

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Identification
Molecular formula
C17H14N2
CAS number
519-23-3
IUPAC name
5,11-dimethyl-6H-pyrido[4,3-b]carbazole
State
State
At room temperature, ellipticine is a solid. It tends to maintain its solid state under ambient conditions, rather than converting to a gas or liquid, given its relatively high melting point.
Melting point (Celsius)
265.00
Melting point (Kelvin)
538.20
Boiling point (Celsius)
515.60
Boiling point (Kelvin)
788.80
General information
Molecular weight
246.31g/mol
Molar mass
246.3060g/mol
Density
1.2500g/cm3
Appearence

Ellipticine appears as a yellow crystalline solid. It is known for its intense yellow color, and the crystals can sometimes display a slight greenish hue under specific lighting conditions.

Comment on solubility

Solubility of 5,11-dimethyl-6H-pyrido[4,3-b]carbazole (C17H14N2)

5,11-dimethyl-6H-pyrido[4,3-b]carbazole is a complex organic compound known for its interesting structural and solubility characteristics. Understanding its solubility is crucial for its potential applications in various fields.

General Solubility Profile

  • Solvent Compatibility: The solubility of this compound tends to depend significantly on the choice of solvent. It exhibits varying degrees of solubility in organic solvents such as chloroform, dichloromethane, and ethanol.
  • Polarity Effects: Given the highly aromatic structure, compounds with lower polarity solvents often yield better solubility. Polar solvents might struggle to dissolve this compound efficiently.
  • Temperature Influence: As with many organic compounds, increasing the temperature generally enhances solubility. It's prudent to consider thermal conditions when attempting to dissolve this compound.

Practical Insights

In laboratory settings, it's often observed that:

  • Concentration matters: Higher concentrations may lead to precipitation.
  • pH Variations: The solubility may also be influenced by the pH of the solution, although the effects can vary depending on the presence of specific functional groups.
  • Crystal Form: The crystallization form of the compound can affect its solubility; exploring different polymorphs can be beneficial.

In summary, the solubility of 5,11-dimethyl-6H-pyrido[4,3-b]carbazole is influenced by a combination of factors such as solvent type, temperature, and concentration. **Optimizing these conditions is essential for effective use in chemical processes.**

Interesting facts

Interesting Facts about 5,11-Dimethyl-6H-pyrido[4,3-b]carbazole

5,11-Dimethyl-6H-pyrido[4,3-b]carbazole is a fascinating compound that has piqued the interest of chemists and researchers alike due to its unique structure and potential applications. Here are some compelling aspects of this compound:

  • Structural Complexity: This compound belongs to a group of polycyclic aromatic heterocycles, showcasing a complex arrangement of carbon and nitrogen atoms. Its unique carbon-nitrogen framework contributes to its intriguing chemical behavior and properties.
  • Biological Relevance: Compounds similar to 5,11-dimethyl-6H-pyrido[4,3-b]carbazole have been studied for their biological activity. Research suggests they may have anti-cancer properties and could be involved in numerous biochemical pathways.
  • Fluorescence: Certain derivatives of this compound exhibit strong fluorescence, making them useful in various applications, including organic light-emitting diodes (OLEDs) and biological imaging techniques.
  • Synthetic Challenge: The synthesis of this compound is not trivial and often requires multistep reactions. This complexity makes it a subject of interest for synthetic chemists looking to develop innovative methods of organic synthesis.

As a compound rich in both chemical diversity and potential, 5,11-dimethyl-6H-pyrido[4,3-b]carbazole stands at the intersection of organic chemistry and materials science. Researchers continue to explore its properties, with the hope that it may lead to advances in both theoretical and applied chemistry.

"Each new compound holds a story waiting to be uncovered." — An Aspiring Chemist

Synonyms
ellipticine
519-23-3
5,11-Dimethyl-6H-pyrido[4,3-b]carbazole
Elliptisine
NSC 71795
5,11-Dimethyl-6H-pyrido(4,3-b)carbazole
TCMDC-125546
NSC-71795
ICIG 770
elliptecine
CCRIS 2003
BRN 0221300
EINECS 208-264-0
CHEBI:4776
UNII-117VLW7484
NSC71795
ELLIPTICINE [MI]
6H-Pyrido(4,3-b)carbazole, 5,11-dimethyl-
6H-Pyrido[4,3-b]carbazole, 5,11-dimethyl-
CHEMBL123
117VLW7484
MLS000028487
MLS000736786
DTXSID30199855
5-23-09-00417 (Beilstein Handbook Reference)
CCG-36483
SMR000058370
5,11-Dimethylpyrido[4,3-b]carbazole
CP 5
SR-01000003083
Ellipticin
Ellipticine?
5,11-Dimethyl-6H-pyrido[4,3-b]carbazole; CP 5; NSC 71795
ellipticine, HCl
5,3-b]carbazole
Prestwick_194
MFCD00010524
Ellipticine, synthetic
Opera_ID_1748
Prestwick0_000614
Prestwick1_000614
Prestwick2_000614
Prestwick3_000614
Lopac-E-3380
Probes1_000152
Probes2_000130
cid_3213
Neuro_000031
Lopac0_000531
REGID_for_CID_3213
BSPBio_000548
MLS001076505
SCHEMBL138079
SPBio_002767
BPBio1_000604
DTXCID90122346
HMS1569L10
HMS2096L10
HMS2230H10
HMS3261L03
HMS3371L09
BCP13208
EX-A2053
Tox21_500531
BDBM50004233
AKOS024457578
CS-5294
LP00531
SDCCGSBI-0050514.P002
CCG36483; NSC71795
NCGC00015411-01
NCGC00015411-02
NCGC00015411-03
NCGC00015411-04
NCGC00015411-05
NCGC00015411-06
NCGC00015411-07
NCGC00015411-08
NCGC00015411-09
NCGC00015411-10
NCGC00015411-12
NCGC00015411-14
NCGC00015411-19
NCGC00022199-03
NCGC00022199-04
NCGC00022199-05
NCGC00261216-01
AC-35834
AS-77042
CAS-519-23-3
HY-15753
NCI60_040685
5,11-dimethyl-2H-pyrido[4,3-b]carbazole
DB-052047
WLN: T D6 B656 FN LMJ C1 J1
EU-0100531
NS00032376
C09154
E 3380
K00071
SR-01000003083-2
SR-01000003083-6
BRD-K85985071-001-03-3
BRD-K85985071-001-16-5
BRD-K85985071-001-22-3
Q10359556