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Isoquinoline-1,3,4-trione

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Identification
Molecular formula
C9H3NO3
CAS number
491-31-6
IUPAC name
isoquinoline-1,3,4-trione
State
State

At room temperature, isoquinoline-1,3,4-trione is a solid. It maintains a stable crystalline structure under standard conditions.

Melting point (Celsius)
271.00
Melting point (Kelvin)
544.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
161.12g/mol
Molar mass
161.1160g/mol
Density
1.5790g/cm3
Appearence

Isoquinoline-1,3,4-trione appears as a pale yellow to yellow crystalline solid. It is relatively stable and has a unique structure, allowing it to have distinctive chemical properties.

Comment on solubility

Solubility of isoquinoline-1,3,4-trione

isoquinoline-1,3,4-trione is a fascinating compound known for its unique structural features. When it comes to solubility, several key points should be highlighted:

  • Solvent Dependence: The solubility of isoquinoline-1,3,4-trione is highly dependent on the type of solvent used. It is generally more soluble in polar solvents such as water and ethanol.
  • Temperature Influence: Increasing the temperature often enhances the solubility of this compound. For example, one might observe that its solubility increases significantly in hot solvents compared to cold.
  • pH Sensitivity: The solubility can also be affected by the pH level of the solution, with certain pH conditions promoting greater solubility due to changes in the compound's ionization state.
  • Complex Formation: isoquinoline-1,3,4-trione can form complexes with various metal ions, which can further influence its solubility in different environments.

In conclusion, the solubility of isoquinoline-1,3,4-trione is a multifaceted property influenced by multiple factors, making it an interesting subject for further study and application in various chemical processes.

Interesting facts

Interesting Facts about Isoquinoline-1,3,4-trione

Isoquinoline-1,3,4-trione is a fascinating compound that falls into the category of isoquinoline derivatives. This compound is notable for its unique ring structure and its potential applications in various fields of research and industry. Here are some interesting aspects to consider:

  • Structural Features: Isoquinoline-1,3,4-trione contains a fused bicyclic framework that contributes to its intriguing chemical properties. The trione functional group adds to its reactivity, making it a subject of interest in synthetic organic chemistry.
  • Biological Activity: Compounds related to isoquinoline structures have been studied for their biological activities, showcasing a range of effects from antimicrobial to anticancer properties. Such activities point to the potential of isoquinoline-1,3,4-trione in pharmaceutical applications.
  • Colorimetric Applications: Due to its specific electronic structure, isoquinoline-1,3,4-trione can be used as a chromogenic reagent. Its ability to change color in response to different conditions makes it valuable in analytical chemistry.
  • Natural Product Synthesis: Isoquinoline-1,3,4-trione may serve as a precursor in the synthesis of more complex natural products, expanding the toolkit of chemists interested in drug discovery and development.
  • Versatile Intermediates: It can act as an important intermediate in organic synthesis, leading to diverse functionalized derivatives that contribute to materials science, such as dyes and pigments.

In conclusion, isoquinoline-1,3,4-trione is not just a simple compound; it embodies a wealth of possibilities in both fundamental and applied chemistry. As scientists continue to explore its potential, isoquinoline-1,3,4-trione stands as a testament to the intricate connections found within organic compounds.

Synonyms
isoquinoline-1,3,4(2H)-trione
521-73-3
isoquinoline-1,3,4-trione
Phthalonimide
1,3,4(2H)-Isoquinolinetrione
1,3,4-(2H)ISOQUINOLINETRIONE
BM68CV5X6Q
NSC-407248
NSC 407248
BRN 0383773
3deh
MFCD01717158
NSC407248
UNII-BM68CV5X6Q
1,2,3,4-tetrahydroisoquinoline-1,3,4-trione
1,4(2H)-Isoquinolinetrione
5-21-11-00575 (Beilstein Handbook Reference)
CHEMBL206435
Isoquinoline-1,3,4-trione 1
SCHEMBL1122624
BDBM10247
DTXSID40200103
AKOS006276226
LS-13574
DB-082869
CS-0149741
D81951
Q27465167
RXA