Sodium 2-(4-allyloxy-3-chlorophenyl)acetate

Identification

Molecular formula

C₁₁H₁₀ClNaO₃

CAS number

73384-59-5

IUPAC name

sodium;2-(4-allyloxy-3-chloro-phenyl)acetate

State

At room temperature, Sodium 2-(4-allyloxy-3-chlorophenyl)acetate exists as a solid. It is stable under standard conditions and does not dissolve readily in water.

Melting point (Celsius)

150.00

Melting point (Kelvin)

423.15

Boiling point (Celsius)

420.00

Boiling point (Kelvin)

693.15

General information

Molecular weight

246.66g/mol

Molar mass

246.6600g/mol

Density

1.2400g/cm³

Appearence

The compound appears as a white to off-white crystalline powder. It is typically odorless, but may have a faint characteristic odor due to the presence of the allyloxy functional group.

Comment on solubility

Solubility of Sodium 2-(4-allyloxy-3-chloro-phenyl)acetate

Sodium 2-(4-allyloxy-3-chloro-phenyl)acetate, a salt formed from a phenylacetate derivative, exhibits interesting solubility characteristics that can be outlined as follows:

Water Solubility: This compound is typically soluble in water due to the presence of the sodium ion, which often increases the solubility of organic compounds in aqueous solutions.
Organic Solvents: It may show higher solubility in polar organic solvents such as ethanol and methanol, given the presence of the ether functional group in its structure.
Temperature Dependence: Solubility can also be influenced by temperature; generally, increased temperature enhances solubility for many salts.
pH Influence: The solubility of this compound could vary with pH, potentially increasing in more basic conditions due to deprotonation of acidic groups.

In summary, the solubility of sodium 2-(4-allyloxy-3-chloro-phenyl)acetate is a complex interplay of its ionic nature, solvent interactions, and environmental conditions. As with many salts, understanding these factors is crucial for its application in various fields.

Interesting facts

Interesting Facts about Sodium 2-(4-Allyloxy-3-chloro-phenyl)acetate

Sodium 2-(4-allyloxy-3-chloro-phenyl)acetate is a fascinating compound that showcases the intersection of organic chemistry and medicinal applications. Here are some noteworthy points:

Structural Complexity: This compound features an intricate structure that includes both an allyloxy group and a chloro-substituted aromatic ring, making it a subject of interest in synthetic organic chemistry.
Potential Therapeutic Uses: Research has indicated that compounds of this class may possess biological activities, leading to exploration within pharmaceutical chemistry for potential applications in drug development.
Versatility: The allyloxy moiety can engage in various chemical reactions, making this compound a useful intermediate in organic synthesis and possibly leading to the development of new derivatives.
Chemical Reactions: The presence of a chloro substituent on the phenyl ring suggests that this compound could participate in nucleophilic substitution reactions, which is a fundamental concept in organic synthesis.
Environmental Impact: As with many chemical compounds, understanding the environmental behavior of sodium 2-(4-allyloxy-3-chloro-phenyl)acetate is crucial for assessing its safety and ecological effects when used in industrial or laboratory settings.

In sum, sodium 2-(4-allyloxy-3-chloro-phenyl)acetate is more than just a chemical entity; it serves as a gateway to discussions on medicinal chemistry, organic synthesis, and environmental considerations. As one would quote, "Every compound tells a story, and this one hints at the potential for a remarkable narrative in the realm of pharmaceuticals."