Ethyl chlorooxoacetate

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Identification

Molecular formula
C4H5ClO3
CAS Number
4858-90-1
IUPAC Name
ethyl 2-chloro-2-oxo-acetate
Molecular Weight
152.56g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2345g/cm3
Synonyms
4755-77-5
Interesting facts

Interesting Facts about Ethyl 2-chloro-2-oxo-acetate

Ethyl 2-chloro-2-oxo-acetate is a fascinating compound with numerous applications in both organic synthesis and various industrial processes. Here are some intriguing aspects of this compound:

  • Synthetic Versatility: This compound is often utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, allowing chemists to create a wide variety of derivatives, making it a valuable building block in organic chemistry.
  • Chirality in Action: The presence of the chloro group in its structure introduces interesting chirality, which can be harnessed in asymmetric synthesis, a technique that is crucial for producing specific enantiomers in drug development.
  • Reactivity: Ethyl 2-chloro-2-oxo-acetate participates in several chemical reactions, including nucleophilic substitutions and acylation, thus extending its utility in various synthetic pathways.
  • Applications in Materials Science: This compound has been explored for its potential role in creating polymeric materials due to its reactive functional groups that can be further modified to tailor properties and enhance performance.
  • Environmental Considerations: As with many chlorinated compounds, researchers are examining its environmental impact, assessing toxicity levels and persistence, which is an important aspect for safe handling and regulation.

Overall, the study of ethyl 2-chloro-2-oxo-acetate provides insightful lessons in chemical reactivity, synthesis, and the broader implications of using such compounds in various fields. As chemists continue to explore its capabilities, this compound remains a significant subject of interest in modern chemistry.

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