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itraconazole

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Identification
Molecular formula
C35H38Cl2N8O4
CAS number
84625-61-6
IUPAC name
buta-1,3-diene-1,1,4-tricarboxylic acid
State
State

Itraconazole is typically a solid at room temperature.

Melting point (Celsius)
166.74
Melting point (Kelvin)
439.89
Boiling point (Celsius)
478.00
Boiling point (Kelvin)
751.15
General information
Molecular weight
705.64g/mol
Molar mass
705.6370g/mol
Density
1.2380g/cm3
Appearence

Itraconazole is a colorless or slightly yellow crystalline powder.

Comment on solubility

Solubility of Buta-1,3-diene-1,1,4-tricarboxylic Acid

Buta-1,3-diene-1,1,4-tricarboxylic acid, with the chemical formula C35H38Cl2N8O4, exhibits distinctive solubility characteristics that are essential for its application in various chemical processes.

Key Solubility Factors:

  • Polarity: The solubility of this compound is influenced by its polar carboxylic acid functional groups which can engage in hydrogen bonding, making it more soluble in polar solvents such as water.
  • Hydrophobic Regions: Due to its hydrocarbon chain, the compound may also show some solubility in non-polar organic solvents.
  • Concentration Sensitivity: The solubility can vary significantly with concentration; lower concentrations tend to dissolve more readily compared to saturating solutions.
  • Temperature Dependence: An increase in temperature generally enhances the solubility of organic compounds by providing energy to overcome intermolecular forces.

In summary, the solubility of buta-1,3-diene-1,1,4-tricarboxylic acid suggests a synergistic balance between its polar and non-polar characteristics, impacting its behavior in both aqueous and organic environments. Understanding these solubility trends is crucial for effective utilization in synthetic applications and reaction mechanisms.

Interesting facts

Interesting Facts about Buta-1,3-diene-1,1,4-tricarboxylic Acid

Buta-1,3-diene-1,1,4-tricarboxylic acid is a fascinating compound that has captivated the attention of chemists for several reasons:

  • Versatile Reactivity: This compound contains three carboxylic acid functional groups, granting it the ability to participate in a variety of chemical reactions, including esterification and decarboxylation.
  • Biological Significance: Compounds like buta-1,3-diene-1,1,4-tricarboxylic acid can mimic natural metabolites in living organisms. Researchers are keen to explore its role in biochemical pathways.
  • Potential Applications: With its unique structure, this compound has potential applications in the development of polymers and medicinal chemistry. It may be used in synthesizing new materials or drugs.
  • Synthesis Challenges: The synthesis of buta-1,3-diene-1,1,4-tricarboxylic acid poses interesting challenges. Its synthetic routes often require advanced organic chemistry techniques, making it a topic of interest for students and researchers alike.
  • Chemical Behavior: The compound’s diene moiety makes it reactive towards electrophiles, providing valuable insight into **conjugated systems**, which are essential in many organic reactions.

As with many chemical compounds, understanding buta-1,3-diene-1,1,4-tricarboxylic acid not only deepens our knowledge of organic chemistry but also opens doors to innovative applications in numerous scientific fields.

Synonyms
DTXSID301344311
1,3-Butadiene-1,1,4-tricarboxylic acid