Interesting facts
Interesting Facts about (2,2,2-trichloro-1-methyl-ethyl) acetate
(2,2,2-trichloro-1-methyl-ethyl) acetate is a fascinating organic compound that combines an ester functional group with a unique chlorinated hydrocarbon structure. Here are some intriguing insights into its properties and applications:
- Applications in Industry: This compound is commonly used as a solvent in paint thinners and varnishes, making it invaluable in various industrial applications. Its ability to dissolve a wide range of substances is due to the presence of ester and chlorine groups.
- Environmental Impact: The presence of chlorine in its structure makes this compound subject to scrutiny regarding its environmental and health effects. Chlorinated compounds can be persistent in the environment, leading to potential bioaccumulation and harmful effects on aquatic life.
- Reactivity: (2,2,2-trichloro-1-methyl-ethyl) acetate can participate in various chemical reactions, including nucleophilic substitutions and hydrolysis. Its reactivity profile opens up pathways for further chemical transformations, which can be leveraged in synthesizing other compounds.
- Safety Precautions: When handling this compound, *appropriate safety measures* should be taken. It is essential to work in well-ventilated areas and use proper personal protective equipment (PPE) to minimize any health risks.
- Historical Significance: Chlorinated compounds like this one have been studied since the early 20th century. Their synthesis and applications have significantly evolved, leading to modern innovations in organic chemistry.
In summary, (2,2,2-trichloro-1-methyl-ethyl) acetate is not only a useful industrial compound but also an essential subject of study in understanding the environmental implications of chlorinated hydrocarbons. As scientists and students delve deeper into its properties, they uncover the complexities of its interactions and applications, paving the way for more sustainable choices in chemical use.
Synonyms
1,1,1-trichloropropan-2-yl acetate
19376-15-9
Acetic acid 1-methyl-2,2,2-trichloroethyl ester
Trichloroisopropyl acetate
Acetic acid, ester with alpha-trichloroisopropanol
BRN 1760560
ACETIC ACID, 1-METHYL-2,2,2-TRICHLOROETHYL ESTER
0-02-00-00130 (Beilstein Handbook Reference)
SCHEMBL27263431
DTXSID00941060
2,2,2-trichloroisopropyl acetate
Solubility of (2,2,2-trichloro-1-methyl-ethyl) acetate
(2,2,2-trichloro-1-methyl-ethyl) acetate, with its distinctive structure, exhibits intriguing solubility characteristics. This compound is known to be moderately soluble in organic solvents such as ethanol, methanol, and acetone, thanks to the presence of the acetate group which facilitates interactions with polar solvents.
However, when it comes to water, the solubility is notably limited. This is primarily due to the hydrophobic nature of the trichloroethyl group, which tends to repel water molecules. As a result, one might observe the following:
The balance between the hydrophilic acetate group and the hydrophobic trichloroethyl group creates a unique solubility profile that is pivotal in various applications. Understanding these solubility properties can guide the use of (2,2,2-trichloro-1-methyl-ethyl) acetate in chemical processes or formulations. In summary, while the compound thrives in organic environments, it shies away from aqueous conditions, showcasing the fascinating interactions at play in chemical solubility.