N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide

Identification

Molecular formula

C₁₃H₁₈N₂O₂

CAS number

4230-98-0

IUPAC name

N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide

State

At room temperature, N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide is typically in a solid state.

Melting point (Celsius)

127.00

Melting point (Kelvin)

400.15

Boiling point (Celsius)

511.60

Boiling point (Kelvin)

784.80

General information

Molecular weight

234.30g/mol

Molar mass

234.3000g/mol

Density

1.0820g/cm³

Appearence

N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide typically appears as a solid at room temperature. The exact color and form may vary, and it should be characterized by additional descriptions of crystalline or amorphous forms if applicable.

Comment on solubility

Solubility of N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide

The solubility of N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide can be influenced by various factors, particularly due to its organic nature and the functional groups present. Here are some critical aspects to consider:

Polarity: The benzoxazine structure introduces both polar and nonpolar characteristics, which can affect solubility in different solvents.
Solvent Compatibility: This compound is likely to exhibit solubility in organic solvents such as ethanol, acetone, and dimethyl sulfoxide (DMSO). However, it may have limited solubility in water due to its hydrophobic pentyl group.
Temperature: Increasing the temperature generally enhances the solubility of most organic compounds, enabling N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide to dissolve more readily under heated conditions.
pH Influence: The ionization state of the carboxamide group can change with pH, potentially improving solubility in alkaline conditions compared to neutral or acidic environments.

In summary, while N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide may not be highly soluble in water, it demonstrates favorable solubility in various organic solvents, making it versatile for applications in organic chemistry. Understanding these solubility characteristics is crucial for effectively handling and utilizing this compound in research and industrial contexts.

Interesting facts

Interesting Facts about N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide

N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide is a fascinating compound that belongs to the family of benzoxazines, which are known for their versatile applications in various fields. Here are some interesting aspects of this compound:

Structural Uniqueness: The compound is characterized by a unique bicyclic structure that includes a 1,4-benzoxazine ring. This distinctive feature contributes to its chemical reactivity and potential applications.
Potential Applications: Compounds like N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide have been researched for use in pharmaceuticals, polymers, and bioactive materials, thanks to their intriguing chemical properties.
Interactions with Biological Systems: Some studies have suggested that benzoxazine derivatives exhibit biological activity, possibly interacting with various biochemical pathways, making them candidates for further research in medicinal chemistry.
Green Chemistry: The synthesis of benzoxazines often involves eco-friendly methodologies, in line with the principles of green chemistry, making them suitable for sustainable practices.

In summary, N-pentyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide not only presents a fascinating structure and promising applications but also reflects the ongoing advancements in the synthesis and development of novel compounds in chemistry. As with many such compounds, its full potential is still being explored, keeping scientists intrigued and motivated to uncover further uses and applications.

Synonyms

AKOS000182800

AKOS017280587