Methyl 5-amino-2-[5-(1,3-dioxoisoindolin-2-yl)pentoxy]benzoate

Identification

Molecular formula

C₂₁H₂₀N₂O₅

CAS number

956461-30-2

IUPAC name

methyl 5-amino-2-[5-(1,3-dioxoisoindolin-2-yl)pentoxy]benzoate

State

The compound is typically a solid at room temperature, existing in crystalline form.

Melting point (Celsius)

183.50

Melting point (Kelvin)

456.65

Boiling point (Celsius)

562.30

Boiling point (Kelvin)

835.45

General information

Molecular weight

368.38g/mol

Molar mass

368.3840g/mol

Density

1.3271g/cm³

Appearence

The compound appears as a solid, typically in the form of a powder. Its color can vary from white to off-white, depending on purity and specific conditions of the sample.

Comment on solubility

Solubility of Methyl 5-amino-2-[5-(1,3-dioxoisoindolin-2-yl)pentoxy]benzoate

The solubility of methyl 5-amino-2-[5-(1,3-dioxoisoindolin-2-yl)pentoxy]benzoate can vary based on several factors, including the solvent used and the temperature. Here are some key points to consider:

Polar vs. Nonpolar Solvents: This compound is likely to exhibit higher solubility in polar solvents due to the presence of amino and carboxyl functional groups.
Temperature Influence: Solubility typically increases with temperature; thus, heating the solvent may improve the dissolution rate.
pH Dependence: The ionization of the amino group may also affect solubility, indicating that a higher or lower pH could lead to variations in solubility.
Hydrogen Bonding: The potential for hydrogen bonding in solution can greatly enhance solubility, suggesting that the presence of hydroxyl or amine groups aids in this process.

In conclusion, while the exact solubility values may remain specific to experimental conditions, understanding these factors can guide researchers in predicting the behavior of methyl 5-amino-2-[5-(1,3-dioxoisoindolin-2-yl)pentoxy]benzoate in various environments. As always, empirical testing is recommended for precise applications.

Interesting facts

Interesting Facts about Methyl 5-amino-2-[5-(1,3-dioxoisoindolin-2-yl)pentoxy]benzoate

Methyl 5-amino-2-[5-(1,3-dioxoisoindolin-2-yl)pentoxy]benzoate is a fascinating compound that belongs to the class of benzoate esters. It possesses a unique combination of structural features that contribute to its intriguing properties and potential applications in various fields. Here are some compelling aspects of this compound:

Diverse Applications: This compound has the potential for use in pharmaceuticals and agrochemicals due to its intricate structure that may exhibit bioactivity.
Structural Complexity: The compound contains a benzoate moiety, which is bonded to an amine group, adding to its reactivity and versatility in chemical modifications.
Isocyclic Components: With a 1,3-dioxoisoindoline motif, this compound is linked to numerous studies focused on the development of novel drug candidates and bioactive molecules.
Green Chemistry: Processes involving methyl esters like this one often align with green chemistry principles, facilitating sustainable practices in organic synthesis.
Research Potential: Ongoing research in medicinal chemistry is targeting the functionalization of compounds similar to methyl 5-amino-2-[5-(1,3-dioxoisoindolin-2-yl)pentoxy]benzoate for enhanced pharmacological attributes.

As scientists continuously explore the potential of such complex organic compounds, they open doors to innovative therapeutic applications and contribute to a deeper understanding of molecular interactions. The beauty of chemical research lies in the capability to engineer and optimize such compounds for better efficacy and safety in real-world applications.

In the words of Sir Isaac Newton, "If I have seen further it is by standing on the shoulders of giants." This echoes the importance of building on existing knowledge to advance our scientific explorations in chemistry.