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(2,4-dinitrophenyl) 2-chloro-2-ethyl-3-methyl-pentanoate

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Identification
Molecular formula
C15H15ClN2O5
CAS number
2082-79-3
IUPAC name
(2,4-dinitrophenyl) 2-chloro-2-ethyl-3-methyl-pentanoate
State
State
The compound is a solid at room temperature, often used in chemical analysis and identification of carbonyl compounds, owing to its stability and solid state.
Melting point (Celsius)
118.10
Melting point (Kelvin)
391.25
Boiling point (Celsius)
352.70
Boiling point (Kelvin)
625.85
General information
Molecular weight
356.74g/mol
Molar mass
356.7440g/mol
Density
1.4235g/cm3
Appearence

The compound is typically a yellow crystalline solid, often in the form of fine powder or distinct crystals.

Comment on solubility

Solubility of (2,4-dinitrophenyl) 2-chloro-2-ethyl-3-methyl-pentanoate

The solubility of (2,4-dinitrophenyl) 2-chloro-2-ethyl-3-methyl-pentanoate can be influenced by several factors, enabling us to assess its behavior in various solvents. This compound, with both hydrophobic and hydrophilic characteristics, presents an intriguing case in the study of solubility:

  • Solvent Polarity: Polar solvents, such as water, may not dissolve this compound effectively due to its hydrophobic segments, while non-polar solvents might promote better solubility.
  • Temperature Dependency: Increasing the temperature generally enhances solubility for many organic compounds. Therefore, careful temperature control could optimize its solubility.
  • Structural Influence: The presence of the dinitrophenyl group introduces acidity, which can affect the compound's solubility in different pH conditions.

It's important to note that empirical studies are essential to determine the exact solubility limits and behavior of this compound. As a rule of thumb, when dealing with solubility:

  • Compounds with similar polarity tend to dissolve in one another.
  • Functional groups play a significant role in solubility characteristics.

In conclusion, while direct values for the solubility of (2,4-dinitrophenyl) 2-chloro-2-ethyl-3-methyl-pentanoate may not be readily available, understanding the factors influencing solubility can provide valuable insights for practical applications and further research.

Interesting facts

Interesting Facts about (2,4-Dinitrophenyl) 2-Chloro-2-Ethyl-3-Methyl-Pentanoate

(2,4-Dinitrophenyl) 2-chloro-2-ethyl-3-methyl-pentanoate, often abbreviated as DNP-chloropentanoate, is a fascinating compound with a variety of intriguing properties and applications. This compound is notable for its use in the field of synthetic organic chemistry and serves as a valuable intermediate in the synthesis of other chemical entities.

Key Characteristics and Applications:

  • Synthetic Utility: DNP-chloropentanoate is commonly used as a reagent in various organic reactions, particularly in the development of pharmaceutical compounds.
  • Biological Relevance: This compound can act as a *partial agonist* in certain biological pathways, making it relevant for research in pharmacology and drug development.
  • Environmental Considerations: As with many chemical compounds, the environmental impact and safe handling of DNP-chloropentanoate are important considerations in both research and industrial applications.

The presence of the dinitrophenyl group in the structure enhances the compound's electrophilic characteristics, allowing for more nuanced reactions with nucleophiles. Additionally, its chlorinated ethyl group provides interesting reactivity profiles that are explored in synthetic pathways.
As a student or researcher in the field, one might consider the implications of such compounds in developing more selective and effective therapeutic agents, highlighting the interconnectedness of chemistry and health sciences.

Research and Development:

  • Studies are ongoing regarding the *biological activities* of DNP-chloropentanoate, particularly in the context of its interaction with other compounds.
  • Its role as an intermediate sheds light on the versatility of chlorinated organic compounds in synthetic methodologies.

In summary, (2,4-dinitrophenyl) 2-chloro-2-ethyl-3-methyl-pentanoate is not just another compound; it's a gateway into the world of organic synthesis, highlighting key principles of molecular interaction and reactivity.

Synonyms
2183-38-2
Thompson-hayward T-H 113-M
TH 113-M
ENT 27,215
2-(1-Methylpropyl)-4,6-dinitrophenyl 2-chlorobutanoate
DTXSID40944434
BUTANOIC ACID, 2-CHLORO-, 2-(1-METHYLPROPYL)-4,6-DINITROPHENYL ESTER
2,4-dinitrophenyl 2-chloro-2-ethyl-3-methylpentanoate