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5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane

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Identification
Molecular formula
C12H14Cl2O2
CAS number
56612-23-2
IUPAC name
5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane
State
State

The compound is a crystalline solid at room temperature. It remains stable under standard conditions and should be handled with care to prevent it from absorbing moisture from the air.

Melting point (Celsius)
74.00
Melting point (Kelvin)
347.15
Boiling point (Celsius)
306.00
Boiling point (Kelvin)
579.15
General information
Molecular weight
244.15g/mol
Molar mass
244.1530g/mol
Density
1.2320g/cm3
Appearence

5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane is a white crystalline solid with a powdery texture. It can appear as shiny crystalline fragments and may clump together under certain storage conditions.

Comment on solubility

Solubility of 5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane

The solubility characteristics of 5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane can be quite interesting due to its unique structure. Generally, the solubility of this compound can be influenced by several factors:

  • Polarity: The presence of chloromethyl groups may increase the polarity of the molecule, which commonly enhances solubility in polar solvents.
  • Hydrogen Bonding: As a dioxane derivative, it can potentially form hydrogen bonds, which may further augment its solubility in water and other polar mediums.
  • Solvent Interactions: The solubility can vary significantly among different solvents; thus, non-polar solvents might not solubilize this compound effectively.

When considering quantitative solubility data, it could be stated that:

  • The compound may exhibit moderate solubility in alcohols and ethers, facilitating interactions due to their similar polar characteristics.
  • Conversely, in non-polar solvents, we might observe limited to no solubility, emphasizing the role of the molecular structure.

In sum, while 5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane displays potential for solubility in polar environments, keep in mind that interactions with various solvents can lead to a wide range of solubility behaviors. As the saying goes, "like dissolves like," which is crucial when predicting solubility outcomes.

Interesting facts

Exploring 5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane

5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane is an intriguing compound within the realm of organic chemistry, especially noted for its unique structure and potential applications. This compound features a dioxane ring, which is a six-membered ring containing two oxygen atoms, contributing to several notable characteristics:

  • Synthetic Applications: The chloromethyl groups in its structure make it a valuable intermediate in organic synthesis. It can participate in various chemical reactions, enabling the formation of different organic compounds.
  • Pharmaceutical Potential: The phenyl ring contributes to the pharmacological properties, making this compound a candidate for drug formulation and development, particularly in targeting specific biological pathways.
  • Material Science: Its dioxane framework is also studied for its potential use in materials science, where derivatives of dioxane can contribute to the creation of novel polymers.
  • Reactivity Characteristics: The presence of chloromethyl groups can enhance the reactivity of the compound, making it useful in nucleophilic substitution reactions, further broadening its applicability in various organic reactions.

Interesting Facts

Here are a few fascinating points to consider regarding 5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane:

  1. The dioxane structure is famous for its ability to stabilize reactive intermediates in organic reactions due to its electron-withdrawing characteristics.
  2. This compound can act as a versatile building block for synthesizing a wide range of aromatic and heterocyclic compounds.
  3. Researchers are actively investigating the implications of dioxane derivatives in the field of bioinformatics, given their potential interactions with biological systems.

As with many organic compounds, the study of 5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane opens avenues for innovation and discovery in chemistry and its related fields. The balance of reactivity and structural complexity makes this compound a point of interest for chemists focused on the synthesis of functionalized organic materials.

Synonyms
6103-09-9
m-DIOXANE, 5,5-BIS(CHLOROMETHYL)-2-PHENYL-
NSC 55262
1,3-Dioxane, 5,5-bis(chloromethyl)-2-phenyl-
BRN 0154618
5,5-Bis(chloromethyl)-2-phenyl-m-dioxane
DTXSID70209902
5-19-01-00491 (Beilstein Handbook Reference)
DTXCID80132393
5,5-bis(chloromethyl)-2-phenyl-1,3-dioxane
NSC-55262
NSC55262
starbld0022474
4XP2GAG4EG
1,3-Dioxane,5,5-bis(chloromethyl)-2-phenyl-
NCIOpen2_002146
AKOS040752976
DS-008343
AG-690/12763542
SR-01000325223
SR-01000325223-1