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Bungarotoxin

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Identification
Molecular formula
C27H31N3O1
CAS number
1408-57-1
IUPAC name
1,1-diethyl-3-(7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea
State
State

At room temperature, bungarotoxin is typically found in a solid state. It is known to be quite stable in typical laboratory settings, which makes it easy to store and transport for research purposes. Due to its solid crystalline form, it does not vaporize or sublimate easily under ambient conditions.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
471.61g/mol
Molar mass
471.6130g/mol
Density
1.2300g/cm3
Appearence

Bungarotoxin is generally found as a solid, crystalline substance. It appears as a white powder under standard conditions, which can be verified using polarizing light microscopy. The crystalline nature is also characterized by specific angles and refractive indices when analyzed through crystallography.

Comment on solubility

Solubility of 1,1-diethyl-3-(7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea

The solubility of 1,1-diethyl-3-(7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea (C27H31N3O1) is influenced by its complex structure and functional groups. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar: Given the significant presence of nitrogen and oxygen in the molecule, it has the potential for polar interactions.
  • Solvent Compatibility: This compound may exhibit varying solubility in different solvents:
    • Water: Likely low solubility due to its organic structure.
    • Organic solvents: Possible better solubility in organic solvents like ethanol or dimethyl sulfoxide (DMSO).
  • Temperature Dependency: As with many organic compounds, its solubility might increase with temperature, making it important to consider when choosing a solvent for application.
  • Hydrogen Bonding: The presence of urea functionality suggests the potential for hydrogen bonding, which can further influence solubility characteristics.

In conclusion, while 1,1-diethyl-3-(7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea may not be highly soluble in water, its behavior in organic solvents presents a nuanced picture that can be tailored based on the intended application. Understanding these factors is essential for effective usage in chemical processes.

Interesting facts

Interesting Facts about 1,1-Diethyl-3-(7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea

This complex compound, featuring a unique structure that combines elements of both urea and indoloquinoline, has sparked significant interest in the field of medicinal chemistry. Here are some intriguing aspects of this compound:

  • Diverse Applications: Compounds like this one are often studied for their potential therapeutic effects, particularly in the realms of anti-cancer and neurological disorders.
  • Structural Complexity: Its intricate structure includes multiple rings and substituents, which can lead to interesting interactions with biological systems and can affect the compound's activity.
  • Indoloquinoline Derivative: The indoloquinoline framework is notable for its biological activity, making the study of this compound relevant for understanding mechanisms of action and bioactivity.
  • Potential for Innovation: Research into analogues of this compound can lead to the discovery of new drugs, as structural modifications can yield differing pharmacological profiles.
  • Scientific Quote: As chemist Linus Pauling once said, “The best way to have a good idea is to have lots of ideas.” Exploring such complex compounds opens the door to numerous innovative possibilities.

In summary, the study of 1,1-diethyl-3-(7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinolin-9-yl)urea is a captivating field that encourages further exploration into its properties and potential benefits in science and medicine. With ongoing research, compounds like this can usher in discoveries that may transform therapeutic approaches.

Synonyms
S-(-)-Lisuride
860177-23-7
140387-89-9
CHEMBL57059
SCHEMBL14507250
DTXSID10860218
DA-67335
L000349
Na(2)-(9,10-Didehydro-6-methylergolin-8-yl)-N,N-diethylurea