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Dibenzyl isophthalate

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Identification
Molecular formula
C22H18O4
CAS number
9003-63-2
IUPAC name
dibenzyl benzene-1,3-dicarboxylate
State
State

At room temperature, dibenzyl isophthalate can exist as a liquid or low-melting solid depending on its specific formulation and purity.

Melting point (Celsius)
37.00
Melting point (Kelvin)
310.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
344.35g/mol
Molar mass
344.3490g/mol
Density
1.1800g/cm3
Appearence

Dibenzyl isophthalate typically appears as a colorless to pale yellow viscous liquid or solid. Its appearance can vary slightly depending on its purity and specific form.

Comment on solubility

Solubility of Dibenzyl Benzene-1,3-Dicarboxylate

Dibenzyl benzene-1,3-dicarboxylate (C17H16O4) exhibits noteworthy solubility characteristics that are important to consider. This compound is generally recognized for its limited solubility in water, which can be attributed to its large hydrophobic (non-polar) benzyl groups. However, it shows a greater affinity for organic solvents.

Solubility Profile

In terms of solubility, dibenzyl benzene-1,3-dicarboxylate can be summarized as follows:

  • Water: Sparingly soluble
  • Organic Solvents: Soluble in common organic solvents such as ethanol, methanol, dichloromethane, and chloroform

This solubility pattern can be explained by the principle of like dissolves like, where the non-polar sections of the molecule engage favorably with similar organic solvents, but struggle to interact effectively with polar water molecules.

Overall, when working with dibenzyl benzene-1,3-dicarboxylate, it is crucial to consider the choice of solvent for any chemical processes or extractions, as its limited aqueous solubility can impact reaction conditions and outcomes. Always remember to consult solvent compatibility charts and consider the polarity of your solvent system!

Interesting facts

Interesting Facts about Dibenzyl Benzene-1,3-Dicarboxylate

Dibenzyl benzene-1,3-dicarboxylate is a fascinating organic compound that belongs to the class of dicarboxylates. This compound is notable for several reasons:

  • Versatile Applications: Dibenzyl benzene-1,3-dicarboxylate is often used in the synthesis of pharmaceuticals and agrochemicals. Its unique structure makes it an excellent building block in organic chemistry.
  • Structural Significance: The presence of two benzyl groups attached to a dicarboxylate moiety bestows the compound with interesting steric and electronic properties, which can be leveraged in various chemical reactions.
  • Role in Research: Scientists often study this compound to understand reaction mechanisms involving dicarboxylate structures, providing insights into more complex organic synthesis processes.
  • Biodegradability: Investigations into the compound highlight its potential environmental benefits, as dicarboxylates are generally more biodegradable compared to other organic compounds. This opens avenues for exploring sustainable chemical processes.
  • Historical Context: The exploration of dibenzyl benzene derivatives has a rich history, with significant contributions from chemists in the early 20th century who were paving the way for modern organic synthesis.

In conclusion, dibenzyl benzene-1,3-dicarboxylate not only serves essential roles in synthetic methodologies but also presents exciting opportunities for future research and applications within the field of organic chemistry.

Synonyms
dibenzyl benzene-1,3-dicarboxylate
16034-14-3
SCHEMBL312910
MFCD03129996
E83185