6,8-Dichloro-3-phenyl-2H-1,3-benzoxazin-4-one

Identification

Molecular formula

C₁₄H₇Cl₂NO₂

CAS number

142426-21-9

IUPAC name

6,8-dichloro-3-phenyl-2H-1,3-benzoxazin-4-one

State

6,8-dichloro-3-phenyl-2H-1,3-benzoxazin-4-one is a solid at room temperature, typically found in a dry, crystalline form.

Melting point (Celsius)

210.00

Melting point (Kelvin)

483.15

Boiling point (Celsius)

472.00

Boiling point (Kelvin)

745.15

General information

Molecular weight

308.10g/mol

Molar mass

308.0990g/mol

Density

1.4500g/cm³

Appearence

The compound 6,8-dichloro-3-phenyl-2H-1,3-benzoxazin-4-one typically presents as a crystalline solid. The precise appearance can vary based on purity and conditions under which the compound is synthesized. It might exhibit a white to pale yellow coloration depending on its form and any impurities present.

Comment on solubility

Solubility of 6,8-dichloro-3-phenyl-2H-1,3-benzoxazin-4-one

The solubility of 6,8-dichloro-3-phenyl-2H-1,3-benzoxazin-4-one in various solvents is a critical aspect to consider in its applications and interactions. Here are some key points regarding its solubility:

Solvent Dependence: This compound tends to show variable solubility in organic solvents, generally exhibiting better solubility in non-polar solvents compared to polar solvents.
Temperature Influence: Increased temperatures often lead to enhanced solubility. For example, solubility might increase in organic solvents as the temperature rises.
Structural Factors: The presence of chlorine and phenyl groups affects the molecular interactions, often leading to hydrophobic characteristics which impact its overall solubility.

It is important to note that while some studies report limited solubility in water, other organic solvents such as dichloromethane or ethyl acetate may greatly enhance its solubility profile. Understanding these solubility characteristics is essential for practical applications and effective formulation in chemical processes.

Interesting facts

Exploring 6,8-Dichloro-3-phenyl-2H-1,3-benzoxazin-4-one

6,8-Dichloro-3-phenyl-2H-1,3-benzoxazin-4-one is a fascinating compound with various applications in the realm of chemistry and beyond. Here are some intriguing facts:

Structure and Functionality: This compound features a benzoxazine ring, a notable structure that is known for its ability to undergo diverse chemical reactions which can lead to the development of novel materials.
Pesticide and Herbicide Applications: Compounds like 6,8-dichloro-3-phenyl-2H-1,3-benzoxazin-4-one are studied for their potential use in agricultural settings, particularly as herbicides, due to their effectiveness in controlling unwanted plant growth.
Biochemical Importance: The presence of the phenyl group in its structure can enhance its biological activity, making it a subject of interest in medicinal chemistry and pharmacology, especially for developing new drug candidates.
Environmental Impact: As with many chlorinated compounds, it is crucial to study its environmental behavior and degradation pathways to assess its safety and potential ecological effects.
Research Interest: The compound is part of ongoing research looking into its synthetic pathways, which can reveal new methods of preparing similar benzoxazine derivatives with improved properties.

As a scientist, one is often drawn to the unique characteristics and potentials of such compounds. The combination of chlorine substituents, the phenyl ring, and the benzoxazin scaffold adds layers of complexity and opportunities for innovation in various fields, from agriculture to pharmaceuticals.

In summary, 6,8-dichloro-3-phenyl-2H-1,3-benzoxazin-4-one exemplifies how intricate molecular designs can lead to real-world applications and prompts further investigation into its chemical properties and effects.

Synonyms

20973-03-9

BRN 1585011

4H-1,3-BENZOXAZIN-4-ONE, 6,8-DICHLORO-2,3-DIHYDRO-3-PHENYL-

6,8-Dichloro-2,3-dihydro-3-phenyl-4H-1,3-benzoxazin-4-one

DTXSID10175157

DTXCID7097648

RefChem:297039