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GSK 3 inhibitor VI

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Identification
Molecular formula
C17H19NO3
CAS number
143170-93-0
IUPAC name
N-(2-phenylethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide
State
State

At room temperature, this compound is solid. It is commonly found as a crystalline powder, which facilitates its handling and measurement for research purposes.

Melting point (Celsius)
158.30
Melting point (Kelvin)
431.45
Boiling point (Celsius)
325.70
Boiling point (Kelvin)
598.85
General information
Molecular weight
282.33g/mol
Molar mass
282.3330g/mol
Density
1.2352g/cm3
Appearence

GSK 3 inhibitor VI is generally a white to off-white powder. It has a crystalline structure indicative of many high-purity organic solids. The compound is typically handled in powder form in laboratory settings.

Comment on solubility

Solubility of N-(2-phenylethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide

The solubility characteristics of N-(2-phenylethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide can be quite intriguing due to its unique molecular structure. This compound presents significant variability in solubility depending on various factors such as temperature and solvent choice.

Key Solubility Features:

  • Polarity: The presence of the carboxamide functional group typically enhances polarity, which can contribute to better solubility in polar solvents like water.
  • Non-Polar Solvents: Conversely, due to the phenyl and benzoxazine rings, the compound may show good solubility in non-polar organic solvents such as chloroform or benzene.
  • Temperature Dependence: It is crucial to consider that solubility can increase with temperature; thus, heating may enhance solubility in various solvents.
  • pH Effects: As a carboxamide, the solubility can vary with pH changes; alkaline conditions may promote better solubility compared to neutral or acidic environments.

Overall, understanding the solubility of N-(2-phenylethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide requires careful consideration of these parameters. Experimentation in different solvents and conditions will often provide the most accurate insights into its practical solubility behavior.

Interesting facts

Interesting Facts about N-(2-phenylethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide

N-(2-phenylethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide, a compound with fascinating structural properties, belongs to the class of benzoxazines, which are significant in both synthetic chemistry and material science. Here are some notable points regarding this compound:

  • Structural Diversity: This compound exhibits a unique molecular architecture, combining features of aromatic and aliphatic systems. The presence of the 1benzoxazine ring contributes to its stability and chemical reactivity.
  • Tunable Properties: Compounds in the benzoxazine family are known for their ability to be tailored for specific applications, such as in polymers. By modifying substituents like the phenyl group, one can potentially enhance characteristics like thermal stability or solubility.
  • Origin of Applications: Benzoxazines have gained attention in the fields of material science, particularly as precursors for thermosetting resins. They can polymerize to form durable materials used in coatings, adhesives, and composites.
  • Biological Relevance: Some derivatives of benzoxazines have shown promising biological activities, making them subjects of pharmaceutical research. The structural similarity to other bioactive compounds supports their further investigation.
  • Mechanistic Insight: Understanding the reactivity of N-(2-phenylethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide can shed light on reaction mechanisms involving nitrogen-containing heterocycles, which are essential in organic synthesis.

In summary, N-(2-phenylethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxamide is not only a compound of structural interest but also holds potential for various applications in **material science** and **pharmaceutical research**. As researchers continue to explore its properties, it paves the way for exciting developments in the world of chemistry.

Synonyms
AKOS000179048
AKOS017281347