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Clausenamid C chloride

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Identification
Molecular formula
C21H26ClN1O4
CAS number
Not Assigned
IUPAC name
1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-ol;chloride
State
State

At room temperature, Clausenamid C chloride is a solid. It maintains its solid state under standard conditions and demonstrates considerable stability when stored appropriately in airtight containers.

Melting point (Celsius)
179.00
Melting point (Kelvin)
452.00
Boiling point (Celsius)
314.00
Boiling point (Kelvin)
587.00
General information
Molecular weight
415.94g/mol
Molar mass
415.9380g/mol
Density
1.3300g/cm3
Appearence

This compound appears as a light yellow to off-white powder. It is fully synthesized in a laboratory environment and can sometimes crystallize out in a defined crystal form.

Comment on solubility

Solubility of 1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-ol; chloride

The solubility of 1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-ol; chloride is an intriguing topic for researchers and chemists alike. This compound exhibits a unique combination of structural features that influence its solubility in various solvents.

Generally, the solubility can be influenced by several factors:

  • Polarity: Due to the presence of multiple methoxy (-OCH3) groups, the compound may show increased solubility in polar solvents.
  • Hydrogen Bonding: The hydroxyl (-OH) functional group in the structure can facilitate hydrogen bonding, potentially enhancing solubility in water and alcohols.
  • Salting Out Effects: The chloride ion may affect solubility, reducing it in concentrations of aqueous solutions due to the "salting out" effect.

It is noted that "like dissolves like," emphasizing that the solubility in organic solvents may vary considerably. The compound is anticipated to have:

  • High solubility in non-polar solvents like dichloromethane and chloroform.
  • Moderate solubility in polar organic solvents such as ethanol and methanol.
  • Lower solubility in water due to its bulky structure.

In conclusion, the solubility of this compound is expected to be a function of its intricate structure, with both polar and hydrophobic interactions playing significant roles. Further experimentation and analysis are necessary to elucidate its precise solubility characteristics.

Interesting facts

1,2,10-Trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-ol; Chloride

This compound is a fascinating member of the class of dibenzoquinolines, known for their complex structures and diverse pharmacological activities. Specifically, it contains a unique arrangement characterized by a quinoline core fused to a cyclic structure. The presence of multiple methoxy groups significantly enhances its chemical reactivity and potential biological activity, making it a subject of interest in medicinal chemistry.

Key Features:

  • Structural Complexity: The intricate arrangement of the fused ring system contributes to its unique chemical properties and interactions.
  • Pharmacological Potential: Compounds of this nature are often researched for their potential applications in treating various diseases, including cancer and neurodegenerative disorders.
  • Mechanism of Action: Studying compounds like this can reveal mechanisms by which complex organic molecules exert their effects in biological systems.

Quote: "The beauty of chemistry lies in the remarkable structures and unpredictable properties that can arise from simple building blocks."

While research on this specific compound is still developing, its structural relatives have demonstrated significant promise in drug discovery. Investigating its synthesis pathways and potential modifications could unveil new avenues for therapeutic development. The ever-evolving field of chemistry continually emphasizes the importance of exploring such intricate compounds, as they often hold the key to new medicinal breakthroughs.


Synonyms
Menisperine chloride
20911-73-3
6a-alpha-APORPHINIUM, 11-HYDROXY-1,2,10-TRIMETHOXY-6-METHYL-, CHLORIDE