1,1,1,3-Tetrachloroacetone
- Molecular formula
- C3H4Cl4O
- CAS Number
- 921-17-1
- IUPAC Name
- 1,1,1,3-tetrachloropropan-2-one
- Molecular Weight
- 194.87g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5600g/cm3
- Synonyms
- 1, 1, 1, 3-TETRACHLOROACETONE
Identification
Interesting Facts about 1,1,1,3-Tetrachloropropan-2-one
1,1,1,3-Tetrachloropropan-2-one, often referred to by its IUPAC name, is a fascinating compound with a variety of intriguing characteristics and applications in the field of chemistry. Here are some key insights:
- Structural Composition: This compound features a carbon backbone flanked by chlorine atoms. The presence of multiple chlorine substituents contributes to its unique chemical reactivity.
- Reactivity: Due to its halogenated structure, 1,1,1,3-tetrachloropropan-2-one is known for its reactivity in nucleophilic substitution reactions. This makes it a valuable intermediate in organic synthesis.
- Applications: It serves various roles in both industrial and laboratory settings, including its use as a solvent, a reagent, and a building block in the synthesis of more complex organic compounds.
- Environmental and Health Considerations: Being a chlorinated compound, it is essential to handle 1,1,1,3-tetrachloropropan-2-one with care, as it may pose health risks and environmental concerns. Studies have been conducted to analyze its toxicity and behavior in biological systems.
- Regulatory Status: Understanding its properties has led to regulations surrounding its use, emphasizing the importance of responsible management of chlorinated compounds in chemical practices.
In summary, 1,1,1,3-tetrachloropropan-2-one exemplifies the complexities of chlorinated organic compounds. Its chemical behavior and practical applications make it a subject of interest among chemists, while also reminding us of the responsibilities tied to chemical usage in industry and research. As we continue to explore the world of chemistry, understanding such compounds can lead to innovation and the development of safer alternatives.