4-Methyl-2-(trichloromethyl)-1,3-dioxolane

Identification

Molecular formula

C₅H₇Cl₃O₂

CAS number

27780-12-3

IUPAC name

4-methyl-2-(trichloromethyl)-1,3-dioxolane

State

At room temperature, 4-Methyl-2-(trichloromethyl)-1,3-dioxolane is typically found in a liquid state. It is volatile and can evaporate if not stored properly.

Melting point (Celsius)

-38.00

Melting point (Kelvin)

235.15

Boiling point (Celsius)

192.00

Boiling point (Kelvin)

465.15

General information

Molecular weight

185.49g/mol

Molar mass

185.4860g/mol

Density

1.4855g/cm³

Appearence

4-Methyl-2-(trichloromethyl)-1,3-dioxolane appears as a colorless liquid. It is known for its clear appearance and is generally used in organic synthesis as an intermediate or solvent.

Comment on solubility

Solubility of 4-methyl-2-(trichloromethyl)-1,3-dioxolane

4-methyl-2-(trichloromethyl)-1,3-dioxolane is a unique compound with interesting solubility characteristics. Its solubility profile can be influenced by several factors:

Polarity: The presence of the trichloromethyl group can increase the polarity of the molecule, which may enhance its solubility in polar solvents.
Solvent Interaction: This compound is likely to be more soluble in solvents such as water and alcohols due to the ability of these solvents to stabilize the polar regions of the molecule.
Temperature Effects: Generally, increasing temperature can improve solubility for many organic compounds, including 4-methyl-2-(trichloromethyl)-1,3-dioxolane, as it promotes greater molecular motion.

However, it is essential to note that while the compound may exhibit some solubility in polar solvents, its compatibility with nonpolar solvents may be limited due to the presence of electronegative chlorine atoms, which creates an imbalance in its structural polarity. As quoted by renowned chemists, "the solubility of a compound largely determines its reactivity and efficiency in various chemical applications."

In practical applications, understanding the solubility of 4-methyl-2-(trichloromethyl)-1,3-dioxolane can be vital for its use in synthesis and formulation processes. Overall, while its polar nature suggests potential solubility in certain environments, detailed empirical studies are necessary to draw conclusive insights.

Interesting facts

Interesting Facts about 4-methyl-2-(trichloromethyl)-1,3-dioxolane

4-methyl-2-(trichloromethyl)-1,3-dioxolane, often referred to as a dioxolane derivative, is a compound that showcases the fascinating interplay of organic chemistry and functional group manipulation. Here are some intriguing aspects of this compound:

Unique Structure: The presence of both a dioxolane ring and a trichloromethyl group in its structure gives this compound distinct chemical properties, influencing its reactivity and interactions.
Applications in Synthesis: Compounds like 4-methyl-2-(trichloromethyl)-1,3-dioxolane are often utilized in organic synthesis, particularly in the formation of various intermediates in the pharmaceutical industry.
Environmental Considerations: The trichloromethyl group is notable for its potential environmental and health implications, as chlorinated compounds can contribute to chemical persistence and bioaccumulation.
Synthesis Pathways: Understanding the synthesis of this compound requires knowledge of electrophilic substitutions and the manipulation of functional groups, making it an excellent example for students studying organic chemistry. As one chemist aptly stated, “Every compound is a journey; it tells the story of its creation."

The exploration of 4-methyl-2-(trichloromethyl)-1,3-dioxolane not only enriches our understanding of complex organic molecules but also highlights the importance of careful handling and study of chlorinated compounds in modern chemistry.

Synonyms

4-methyl-2-(trichloromethyl)-1,3-dioxolane

4353-02-0

SC-1690

BRN 0107136

2-(Trichloromethyl)-4-methyl-1,3-dioxolane

1,3-DIOXOLANE, 4-METHYL-2-(TRICHLOROMETHYL)-

4-19-00-00055 (Beilstein Handbook Reference)

DTXSID60963021