Skip to main content

Budesonide

ADVERTISEMENT
Identification
Molecular formula
C25H34O6
CAS number
51333-22-3
IUPAC name
[2-(11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl] 3,3-dimethylbutanoate
State
State

At room temperature, Budesonide is a solid.

Melting point (Celsius)
224.00
Melting point (Kelvin)
497.15
Boiling point (Celsius)
571.15
Boiling point (Kelvin)
844.30
General information
Molecular weight
430.53g/mol
Molar mass
430.5340g/mol
Density
1.2500g/cm3
Appearence
Budesonide is a white to off-white crystalline powder.
Comment on solubility

Solubility Analysis

The compound [2-(11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl] 3,3-dimethylbutanoate presents a complex structure, indicating unique solubility characteristics. The solubility of such compounds can vary significantly based on several factors:

  • Polarity: Compounds with polar functional groups, such as hydroxyls, tend to have higher solubility in polar solvents like water.
  • Size and Steric Hindrance: Larger molecules may exhibit reduced solubility due to steric effects that hinder interactions with solvent molecules.
  • Hydrogen Bonding: The presence of hydroxyl groups can lead to enhanced solubility in protic solvents due to hydrogen bond formation.
  • Solvent Effects: The choice of solvent plays a critical role; for instance, non-polar solvents may dissolve non-polar parts of the molecule better.

As a result, it’s important to consider both the chemical structure and the environment when predicting solubility. In general, compounds with similar functional groups often exhibit similar solubility trends. Given the intricate structure of this compound, one might expect intermediate to low solubility in non-polar solvents while possibly achieving good solubility in alcohols or other polar solvents. This indicates the necessity for thorough solubility testing in different media.

In summary, understanding the solubility of this complex compound requires a multi-faceted approach, taking into account its physicochemical properties, potential for hydrogen bonding, and the choice of solvent.

Interesting facts

Interesting Facts about 2-(11,17-Dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl 3,3-dimethylbutanoate

This compound is a fascinating example of the complexity that can arise in chemical compounds, particularly in the realm of organic chemistry. It features a unique structure that incorporates multiple functional groups, attributes which might lead one to explore its biological significance and potential therapeutic applications.

Key Features

  • Cyclic Structure: The compound contains a cyclopenta[a]phenanthren core, indicating that it originates from a class of polycyclic aromatic hydrocarbons that are often found in natural products.
  • Hydroxyl Groups: The presence of dihydroxy functionalities at specific positions suggests potential for considerable reactivity and interaction with biological systems, contributing to its potential medicinal properties.
  • Modified Ester Linkage: The ester part of the molecule (3,3-dimethylbutanoate) hints at potential bioactivity, especially as esters are often utilized in medicinal chemistry to enhance the lipophilicity and absorbability of compounds.

Such compounds often serve as crucial intermediates in the synthesis of pharmaceuticals or other biologically active molecules. As noted by scientists in the field, "The diversity of structures and the resulting activities reflect the intricate relationship between molecular configuration and biological function."

Potential Applications

Given its structural attributes, this compound may warrant investigation for:

  • Anticancer Activity: Due to its complex arrangement, it could potentially interfere with cellular processes.
  • Endocrine Modulation: Compounds with similar backbones have been studied for their effects on hormone pathways.
  • Anti-inflammatory Properties: The hydroxyl groups might play a role in reducing inflammation by modulating immune response.

In summary, the deep structural intricacies of this compound provide a wealth of opportunity for research and development in medicinal chemistry, potentially leading to novel discoveries in the realm of pharmaceuticals.

Synonyms
11beta,17,21-Trihydroxypregn-4-ene-3,20-dione 21-(3,3-dimethylbutyrate)
DTXSID80871715
11,17-dihydroxy-3,20-dioxopregn-4-en-21-yl 3,3-dimethylbutanoate