(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
Molecular Weight
356.74g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4235g/cm3
Synonyms
2183-38-2
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.

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