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Carisoprodol

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Identification
Molecular formula
C12H18N2O4
CAS number
78-44-4
IUPAC name
(4-acetamidophenyl) isopropyl carbonate
State
State

At room temperature, Carisoprodol is in a solid state, typically available as tablets for medical use.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
260.34g/mol
Molar mass
260.3350g/mol
Density
1.1400g/cm3
Appearence

Carisoprodol appears as a white, crystalline powder. It is odorless and has a bitter taste.

Comment on solubility

Solubility of (4-acetamidophenyl) isopropyl carbonate

(4-acetamidophenyl) isopropyl carbonate, known for its unique structure, exhibits interesting solubility characteristics that are important in various applications. Generally, the solubility of this compound can be influenced by several factors:

  • Polarity: The presence of polar functional groups, such as the acetamido group, often allows for better solubility in polar solvents like water, while non-polar components can enhance solubility in organic solvents.
  • Temperature: Increasing temperature typically improves the solubility of solids in liquids. Thus, heating may help dissolve (4-acetamidophenyl) isopropyl carbonate in suitable solvents.
  • pH Level: The solubility can be altered with changes in pH, particularly if the compound can ionize or form complexes with ions in solution.

In practical terms, you may find that:

  • This compound is readily soluble in common organic solvents, making it suitable for reactions or formulations requiring organic media.
  • However, it exhibits limited solubility in water due to its hydrophobic isopropyl group, which can impede interaction with polar water molecules.

In summary, understanding the solubility of (4-acetamidophenyl) isopropyl carbonate is crucial for its effective use in chemical processes. As with many compounds, **"like dissolves like,"** so selecting the right solvent will greatly influence the compound's solubility behaviors.

Interesting facts

Interesting Facts about (4-acetamidophenyl) isopropyl carbonate

(4-acetamidophenyl) isopropyl carbonate is a fascinating chemical compound that belongs to the class of carbonates. Its unique structure and functional groups make it notable for various applications in organic chemistry.

Key Characteristics

  • Functional Groups: This compound features an amide functional group, which can influence the reactivity and properties of the compound. The presence of the carbonate moiety contributes to its stability and potential applications.
  • Potential Applications: The compound may serve as an intermediate in the synthesis of pharmaceuticals or as a versatile reagent due to its carbonate functionality. It can also be investigated for its role in drug delivery systems.
  • Research Opportunities: The unique combination of the acetamido and phenyl groups opens avenues for research in medicinal chemistry, especially regarding potential therapeutic effects and structure-activity relationships.

Significance in Synthetic Chemistry

The synthesis of carbonates is an essential aspect of organic chemistry, with (4-acetamidophenyl) isopropyl carbonate representing a salient example. Its synthesis methods can provide insights into the manipulation of carbonate linkages, which are pertinent in polymer chemistry and material science.

Quote to Ponder

As John C. McKinsey once said, “Chemistry is the “central science” that bridges other natural sciences.” The study of compounds like (4-acetamidophenyl) isopropyl carbonate illustrates the interconnectivity of chemistry, biology, and material science.

In summary, (4-acetamidophenyl) isopropyl carbonate stands out due to its interesting structure and potential applications in drug development. Continued research on such compounds is crucial in unearthing novel therapeutic agents and advancing chemical knowledge.

Synonyms
4-Acetamidophenyl isopropyl carbonate
BRN 2736428
17239-27-9
DTXSID50169272
CARBONIC ACID, ISOPROPYL ESTER, ESTER with 4'-HYDROXYACETANILIDE
DTXCID1091763