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4-Chloro-1,3-dioxan-2-one

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Identification
Molecular formula
C4H5ClO3
CAS number
39620-13-4
IUPAC name
4-chloro-1,3-dioxan-2-one
State
State

At room temperature, 4-Chloro-1,3-dioxan-2-one is in a solid state.

Melting point (Celsius)
88.00
Melting point (Kelvin)
361.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
136.54g/mol
Molar mass
136.5410g/mol
Density
1.3832g/cm3
Appearence

4-Chloro-1,3-dioxan-2-one typically appears as a white crystalline solid. It is characterized by its distinct molecular structure which contributes to its physical properties.

Comment on solubility

Solubility of 4-chloro-1,3-dioxan-2-one

The compound 4-chloro-1,3-dioxan-2-one, known for its unique structure, exhibits interesting solubility properties that are important to consider in various chemical applications.

In general, the solubility of this compound can be influenced by a number of factors, including:

  • Polarity: The presence of chlorine and the dioxan ring contributes to a certain degree of polarity, which may enhance its solubility in polar solvents.
  • Solvent Type: It is commonly soluble in organic solvents such as dichloromethane and acetone, while showing limited solubility in water.
  • Temperature: As with many organic compounds, an increase in temperature generally leads to an increase in solubility.

Additionally, empirical studies suggest that "like dissolves like" applies here, meaning that the compound is more likely to dissolve in solvents with similar polarity characteristics.

To sum up, while 4-chloro-1,3-dioxan-2-one shows some solubility in specific organic solvents, its interaction with water is considerably less favorable, making it an intriguing subject for further exploration in chemical solubility dynamics.

Interesting facts

Interesting Facts about 4-Chloro-1,3-Dioxan-2-One

4-Chloro-1,3-dioxan-2-one is a fascinating compound that has garnered attention in both academic research and industrial applications. Here are some intriguing points about this compound:

  • Structural Uniqueness: 4-Chloro-1,3-dioxan-2-one features a dioxane ring, which is a six-membered ether containing two oxygen atoms within the ring itself. This unique structure gives rise to interesting chemical behaviors and properties.
  • Chlorine Substitution: The presence of the chlorine atom enhances the reactivity of the compound, making it useful in organic synthesis and pharmaceuticals. The chlorinated derivatives often exhibit altered biological activity compared to their non-chlorinated counterparts.
  • Applications in Synthesis: This compound can be utilized as an intermediate in the synthesis of various complex molecules, including agrochemicals and drug compounds, making it an important building block in synthetic chemistry.
  • Research Potential: Ongoing studies focus on understanding the mechanisms and pathways influenced by 4-chloro-1,3-dioxan-2-one, particularly in fields such as medicinal chemistry where chlorinated compounds are often more potent.

In short, the distinct features and potential applications of 4-chloro-1,3-dioxan-2-one make it a compound of significant interest in the realm of chemistry. As scientists continue to explore its capabilities, it is likely that we will discover even more fascinating aspects of this unique molecule.

Synonyms
Epichlorohydrin carbonate
NSC 76035
BRN 0111159
Carbonic acid, (chloromethyl)ethylene ester
CARBONIC ACID, CYCLIC 3-CHLOROPROPYLENE ESTER
5-19-04-00023 (Beilstein Handbook Reference)
Carbonic acid, cyclic (chloromethyl)ethylene ester (7CI,8CI)
DTXCID601023332
Carbonic acid, (chloromethyl)ethylene ester (6CI)
dtxsid30883848
SCHEMBL14890299
Carbonic acid, cyclic (chloromethyl)ethylene ester