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Indometacin farnesil

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Identification
Molecular formula
C36H48ClNO4
CAS number
3581-85-3
IUPAC name
3,7,11-trimethyldodeca-2,6,10-trienyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate
State
State

At room temperature, Indometacin farnesil is in a solid state. It is usually stored in a well-sealed container to protect it from moisture and from the atmosphere.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
467.15
Boiling point (Kelvin)
740.30
General information
Molecular weight
677.21g/mol
Molar mass
677.1880g/mol
Density
1.2700g/cm3
Appearence

Indometacin farnesil typically appears as an off-white to pale yellow crystalline solid. It is often odourless or may have a slight characteristic odor. The compound is usually supplied as a powder form for medicinal use.

Comment on solubility

Solubility of 3,7,11-trimethyldodeca-2,6,10-trienyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate

The solubility characteristics of the compound with the formula C36H48ClNO4 can be quite intriguing due to its complex structure. As a large organic molecule featuring multiple aromatic rings and polar functional groups, its solubility is influenced by several factors:

  • Polarity: The presence of the 4-chlorobenzoyl and methoxy groups can affect the overall polarity. Generally, polar compounds have better solubility in polar solvents.
  • Hydrophobic Regions: The long alkyl chain (dodeca) gives rise to hydrophobic characteristics, potentially impacting solubility in aqueous environments.
  • Solvents: Typically, such compounds may show better solubility in organic solvents like dimethyl sulfoxide (DMSO), ethanol, or acetone rather than in water.
  • Temperature Effects: Increased temperature can enhance solubility for many organic compounds, which may also apply to this particular compound.

In many instances, the specific solubility data is context-dependent, meaning it can vary greatly based on concentration, temperature, and the presence of other solutes. To summarize, the solubility of C36H48ClNO4 demands consideration of its molecular structure and the environment in which it exists.

Interesting facts

Interesting Facts about 3,7,11-trimethyldodeca-2,6,10-trienyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate

The compound 3,7,11-trimethyldodeca-2,6,10-trienyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate is a fascinating example of complex organic chemistry, combining multiple functional groups that contribute to its unique properties. Here are some engaging facts about this compound:

  • Synthetic Roots: This compound showcases the beauty of synthetic organic chemistry, illustrating how chemists can design and construct complex molecules through deliberate manipulation of molecular subunits.
  • Diverse Applications: Compounds with such intricate structures are often explored for their potential use in pharmaceuticals, agrochemicals, and materials science, potentially exhibiting biological activity or serving as intermediates in the synthesis of other valuable compounds.
  • Indole Derivatives: The presence of an indole moiety in this compound suggests significant biological relevance, as indoles are widely recognized for their roles in various natural products and pharmaceuticals. They often contribute to anti-cancer, anti-inflammatory, and anti-viral activities.
  • Chlorobenzoyl Influence: The 4-chlorobenzoyl group enhances hydrophobicity and may improve the interaction of the molecule with biological membranes, potentially impacting its pharmacokinetics.
  • Mesomeric Effects: The π-conjugation resulting from the diene system can lead to unique electronic properties, affecting how the compound interacts with light and other compounds.

In summary, 3,7,11-trimethyldodeca-2,6,10-trienyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate is not only a testament to the creativity of chemists but also exemplifies the connectivity between molecular structure and function in the realm of chemical compounds.

Synonyms
E 0710; IM-F; Indometacin farnesil