2,2-dichloro-1-(2-chlorophenyl)ethanol
- Molecular formula
- C8H7Cl3O
- CAS Number
- 935-56-8
- IUPAC Name
- 2,2-dichloro-1-(2-chlorophenyl)ethanol
- Molecular Weight
- 211.49g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4500g/cm3
- Appearance
- can vary based on the presence of any impurities.
- Synonyms
- 27683-60-9
Identification
Interesting Facts about 2,2-Dichloro-1-(2-chlorophenyl)ethanol
2,2-Dichloro-1-(2-chlorophenyl)ethanol is a fascinating organic compound with a range of intriguing applications and properties that make it noteworthy in the field of chemistry. This compound is a derivative of chlorophenol and contains multiple chlorine substituents, which significantly impact its chemical reactivity and stability.
Chemical Structure and Properties
The unique structure of 2,2-dichloro-1-(2-chlorophenyl)ethanol leads to several important characteristics:
- Chirality: The compound features a chiral center, which allows for the existence of different stereoisomers, potentially impacting its biological activity and pharmacological properties.
- Reactivity: The presence of chlorine atoms makes this compound reactive in nucleophilic substitution reactions, enabling various synthetic pathways in organic chemistry.
Applications
This compound finds use in various fields, including:
- Pesticides: Owing to its chlorinated structure, it serves as an active ingredient in some insecticides, showcasing its potential in agricultural chemistry.
- Pharmaceuticals: The dichloro- and chlorophenyl-groups can influence the biological mechanisms of drug candidates, making this compound a point of interest in medicinal chemistry.
Safety and Environmental Considerations
Due to its chlorinated nature, 2,2-dichloro-1-(2-chlorophenyl)ethanol must be handled with caution:
- Regulatory Concerns: Compounds with chlorine substituents often face scrutiny regarding their environmental impact and potential toxicity.
- Research Focus: Ongoing studies are necessary to understand the metabolic pathways and ecological consequences of its use and degradation products.
In conclusion, 2,2-dichloro-1-(2-chlorophenyl)ethanol embodies a blend of chemical complexity and practical application, making it a subject of ongoing interest among chemists and researchers engaged in organic synthesis and its uses across various industries.