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Ethyl 2-(2,4,6-tribromophenoxy)acetate

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Identification
Molecular formula
C10H9Br3O3
CAS number
26172-54-3
IUPAC name
ethyl 2-(2,4,6-tribromophenoxy)acetate
State
State

At room temperature, ethyl 2-(2,4,6-tribromophenoxy)acetate is typically in a solid state.

Melting point (Celsius)
85.00
Melting point (Kelvin)
358.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
430.90g/mol
Molar mass
430.8970g/mol
Density
1.9000g/cm3
Appearence

Ethyl 2-(2,4,6-tribromophenoxy)acetate is typically a solid compound with a crystalline structure. It is usually white or off-white in color.

Comment on solubility

Solubility of Ethyl 2-(2,4,6-tribromophenoxy)acetate

Ethyl 2-(2,4,6-tribromophenoxy)acetate demonstrates some intriguing properties when it comes to solubility. Being a brominated compound, its behavior in various solvents can be quite distinct. Here are some key observations:

  • Polar Solvents: Compounds similar to ethyl 2-(2,4,6-tribromophenoxy)acetate may show limited solubility in polar solvents like water due to their hydrophobic character influenced by the multiple bromine atoms.
  • Non-Polar Solvents: However, in non-polar solvents such as hexane or benzene, this compound is expected to exhibit greater solubility because of its non-polar characteristics, attributed to the aromatic content and ethyl group.
  • Temperature Dependence: The solubility of many organic compounds often increases with temperature, making it beneficial to consider heating when solubilizing this compound in solvents.
  • Concentration Factors: It is essential to note that at higher concentrations, the solubility may decrease due to intermolecular forces, leading to precipitation or phase separation.

In summary, while ethyl 2-(2,4,6-tribromophenoxy)acetate may find itself more soluble in organic, non-polar environments, its limited compatibility with polar solvents underscores the significance of solvent choice in its application. As the saying goes, “like dissolves like,” emphasizing the importance of understanding polarity in solubility phenomena.

Interesting facts

Interesting Facts about Ethyl 2-(2,4,6-tribromophenoxy)acetate

Ethyl 2-(2,4,6-tribromophenoxy)acetate, often referred to simply as a brominated aromatic compound, stands out due to its unique structural features and potential applications. Here are some fascinating aspects of this compound:

  • Bromine Atoms: The presence of three bromine atoms on the phenoxy ring makes this compound a notable representative of brominated organic compounds. This feature significantly impacts its chemical reactivity and physical properties.
  • Applications in Research: Compounds like ethyl 2-(2,4,6-tribromophenoxy)acetate are of interest in pharmaceuticals and agrochemicals due to their potential use as intermediates in the synthesis of more complex molecules.
  • Environmental Impact: As with many brominated compounds, one must consider the environmental implications, particularly regarding persistence and bioaccumulation. Their utility is offset by potential ecological risks, making proper handling essential.
  • Mechanism of Action: Research suggests that brominated compounds can exhibit specific biological activities, such as antimicrobial properties, which makes them intriguing for further investigations.

This compound exemplifies the complexity of organic chemistry, highlighting the balance between utility and environmental stewardship. As a nascent student of chemistry, one might say, "Exploring compounds like ethyl 2-(2,4,6-tribromophenoxy)acetate opens doors to understanding intricate molecular interactions and their broader implications."

In conclusion, ethyl 2-(2,4,6-tribromophenoxy)acetate serves as a striking example of how modifications at the molecular level can lead to diverse chemical properties and applications, reminding us of the endless possibilities within the field of chemistry.

Synonyms
BRN 1884300
Ethyl 2,4,6-tribromophenoxyacetate
26203-81-6
ACETIC ACID, (2,4,6-TRIBROMOPHENOXY)-, ETHYL ESTER
DTXSID50180841
0-06-00-00205 (Beilstein Handbook Reference)
RefChem:316115
DTXCID90103332
AKOS009143420