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Tetramethoxyphenanthroindolizine

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Identification
Molecular formula
C21H23NO4
CAS number
.
IUPAC name
2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine
State
State

At room temperature, Tetramethoxyphenanthroindolizine is a solid. It is insoluble in water but may dissolve in organic solvents like chloroform or methanol.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
414.50
Boiling point (Kelvin)
687.65
General information
Molecular weight
357.42g/mol
Molar mass
357.3720g/mol
Density
1.2412g/cm3
Appearence

Tetramethoxyphenanthroindolizine is a solid with a crystalline structure. It typically appears as a white to off-white powder, although slight variations in color can occur depending on purity and the presence of impurities.

Comment on solubility

Solubility of 2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine

The solubility of 2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine is influenced by several factors due to its complex structure. Understanding its solubility is crucial for practical applications, particularly in pharmaceutical chemistry and material science. Here are some key points regarding its solubility:

  • Solvent Type: This compound may exhibit varying degrees of solubility in different organic solvents. For instance, it is likely to be more soluble in polar aprotic solvents, such as dimethyl sulfoxide (DMSO) or acetonitrile.
  • Temperature Dependence: The solubility can increase with temperature, which is a common trend for many organic compounds, suggesting that heating the solution may facilitate dissolution.
  • Molecular Interactions: Intermolecular forces, such as hydrogen bonding and van der Waals interactions, play a significant role in solubility. The presence of methoxy groups can enhance solubility by disrupting the crystal lattice of the solid phase.
  • Concentration Effects: At higher concentrations, solubility can be markedly different. Pay attention to saturation concentrations and precipitation thresholds when working with solutions of this compound.

In summary, while this compound presents intriguing possibilities due to its structure, predicting its solubility requires careful consideration of both the solvent conditions and the interactions at play. A systematic approach to experimenting with different solvents and conditions is recommended to fully understand the solubility characteristics of 2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine.

Interesting facts

Interesting Facts about 2,3,5,6-Tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine

This fascinating compound, known for its complex structure and intriguing properties, offers a wealth of insights into organic chemistry. Below are several key points to consider:

  • Structural Complexity: The name itself is a testament to its intricate structure, featuring multiple methoxy groups and a hexahydrophenanthro framework. This complexity can pique interest in synthetic pathways and the challenges associated with creating such compounds.
  • Potential Biological Activity: Compounds with similar frameworks often showcase a variety of biological activities, making this compound a potential candidate for medicinal research. Its unique arrangements of functional groups could interact with biological systems in novel ways.
  • Importance in Material Science: The incorporation of such polycyclic compounds may lead to advancements in materials science. For instance, they could be relevant in the development of organic photovoltaics or molecular sensors due to their electronic properties.
  • Synthetic Challenges: Synthesizing compounds like 2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine involves navigating numerous chemical reactions and conditions, providing an excellent case study for organic chemistry students interested in mastery of synthetic methods.
  • Interdisciplinary Applications: Its potential extends beyond just chemistry; researchers in fields such as pharmacology, nanotechnology, and even environmental science might find uses for this compound, especially in the development of sustainable materials or drug design.

With its multidimensional applications and complex nature, 2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine exemplifies why the study of chemical compounds is both challenging and exciting.

Synonyms
Tylocrebrine DL-form [MI]
UNII-OOF3X9JZ8Q
OOF3X9JZ8Q
30061-35-9
Dibenzo(f,h)pyrrolo(1,2-b)isoquinoline, 9,11,12,13,13a,14-hexahydro-2,3,5,6-tetramethoxy-
2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro[9,10-f]indolizine
2,3,5,6-tetramethoxy-9,11,12,13,13a,14-hexahydrophenanthro(9,10-f)indolizine
(+-)-Tylocrebrine
TYLOCREBRINE DL-FORM
TYLOCREBRINE, (+-)-
DIBENZO(F,H)PYRROLO(1,2-B)ISOQUINOLINE, 9,11,12,13,13A,14-HEXAHYDRO-2,3,5,6-TETRAMETHOXY-, (+-)-
(+/-)-Tylocrebrine
Tylocrebrine, (+/-)-
Dibenzo(f,H)pyrrolo(1,2-b)isoquinoline, 9,11,12,13,13a,14-hexahydro-2,3,5,6-tetramethoxy-, (+/-)-
2,3,5,6-Tetramethoxy-9,11,12,13,13a,14-hexahydrodibenzo[f,h]pyrrolo[1,2-b]isoquinoline
(-)-Tylocrebrin
TYLOCREBIN-(+)
SCHEMBL673888
DTXSID80871937
Q27285759