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7-Methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione

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Identification
Molecular formula
C13H11NO4
CAS number
112306-26-4
IUPAC name
7-methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione
State
State

At room temperature, 7-Methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione is in a solid state. It is typically found in a dry, crystalline form, which ensures stability and ease of handling during experiments and industrial applications. The substance's unique chemical structure contributes to its resistance to ambient environmental conditions.

Melting point (Celsius)
213.00
Melting point (Kelvin)
486.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
261.23g/mol
Molar mass
261.2310g/mol
Density
1.3590g/cm3
Appearence

7-Methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione is a crystalline solid. It typically appears as a brightly colored compound, which may vary from yellow to light brown, depending on its purity and the specific method of crystallization used.

The compound is generally stable under normal conditions, but it should be handled with care to avoid the degradation of its distinctive structure.

Comment on solubility

Solubility of 7-methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione

The solubility of 7-methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione, with the molecular formula C13H11NO4, is an intriguing subject of discussion due to its unique structural characteristics. This compound, like many isoquinoline derivatives, exhibits varying solubility profiles depending on the solvent used. Here are a few notable points regarding its solubility:

  • Polar Solvents: Compounds with amine and ketone functional groups, like this isoquinoline derivative, can show enhanced solubility in polar solvents such as water and methanol. However, the overall solubility may still be limited compared to simpler polar compounds.
  • Non-polar Solvents: Conversely, the presence of the aromatic ring can make 7-methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione more soluble in non-polar solvents like chloroform or benzene, but the solubility may still not be high due to possible molecular interactions.
  • pH Influence: The solubility can be significantly affected by pH. In acidic or basic solutions, the ionization of the amine group could potentially increase the solubility, making it more favorable for dissolution in particular environments.

In conclusion, while this compound does not fall into the highly soluble category for all solvents, its solubility properties are dependent on a myriad of factors including the solvent characteristics and environmental conditions. Thus, experimentation is often necessary to determine precise solubility limits.

Interesting facts

Exploring 7-Methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione

7-Methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione is a fascinating compound that belongs to the isoquinoline class of alkaloids. This class is known for its structural diversity and profound biological activity. Here are some interesting facts:

  • Source of Inspiration: Isoquinolines are often isolated from a variety of plants, many of which have been used in traditional medicine. The presence of the methyl and methoxy groups in this compound can influence its biological properties, making it a subject of interest in pharmacology.
  • Potential Biological Activity: Research has suggested that isoquinoline derivatives may exhibit various pharmacological activities, such as antimicrobial, anti-inflammatory, and anticancer properties. The specific structural modifications in 7-methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione may lead to unique biological profiles that could be explored in drug development.
  • Photochemical Properties: Some studies have indicated that compounds with similar structures can exhibit interesting photochemical properties. This means that they may have applications in fields such as phototherapy or photochemistry, where light is used to initiate chemical reactions.
  • Importance in Organic Chemistry: The study of compounds like 7-methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione is significant for its synthetic routes. Understanding the synthesis of these compounds can lead to better methodologies and strategies in organic synthesis.

As a scientist or a student, exploring the intricacies of 7-methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione can serve as a bridge to understanding complex reactions and interactions within chemical systems. Every molecule has a story, and this compound is no exception!

Synonyms
Mimosamycin
59493-94-6
7-methoxy-2,6-dimethylisoquinoline-3,5,8-trione
7-Methoxy-2,6-dimethyl-3,5,8(2H)-isoquinolinetrione
BRN 0404588
5-21-13-00478 (Beilstein Handbook Reference)
SCHEMBL600128
BXQZTMMXFKFJIY-UHFFFAOYSA-
3,5,8(2H)-Isoquinolinetrione, 7-methoxy-2,6-dimethyl-
DTXSID70208192
CHEBI:223332
3,5,8(2H)-ISOQUINOLINETRIONE, 2,6-DIMETHYL-7-METHOXY-
CCG-257552
7-methoxy-2,6-dimethyl-isoquinoline-3,5,8-trione
InChI=1/C12H11NO4/c1-6-10(15)7-4-9(14)13(2)5-8(7)11(16)12(6)17-3/h4-5H,1-3H3