Ethyl chlorooxoacetate
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- 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
Identification
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.