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Nitrobenzoxazinyl ethyl carbamate

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Identification
Molecular formula
C11H13N3O5
CAS number
127067-15-6
IUPAC name
2-(7-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethyl carbamate
State
State

This compound is typically in a solid state at room temperature.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
268.24g/mol
Molar mass
268.2430g/mol
Density
1.4310g/cm3
Appearence

This compound is typically a pale-yellow crystalline powder. The color may vary slightly based on particle size and purity.

Comment on solubility

Solubility Profile of 2-(7-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethyl carbamate

The solubility of 2-(7-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethyl carbamate can be influenced by several factors. Understanding these factors is crucial for its applications in various fields.

  • Polarity: The presence of nitro and carbamate functional groups can increase polarity, which may enhance solubility in polar solvents like water.
  • Solvent Interactions: This compound may display differing solubility profiles in various solvents. For example, it might dissolve better in dimethyl sulfoxide (DMSO) and alcohols compared to nonpolar solvents.
  • Temperature Effects: Generally, increased temperature can enhance solubility, making it crucial to evaluate solubility at different temperatures for optimal conditions.
  • pH Levels: The solubility may also be affected by the pH of the solution, particularly due to the presence of the carbamate group, which can exist in different forms depending on the acidity or basicity of the environment.

As with many complex compounds, a thorough understanding of its solubility can aid in predicting behavior in different environments and guiding practical applications. It is paramount to perform empirical testing to determine the exact solubility characteristics under relevant conditions.

Interesting facts

Interesting Facts about 2-(7-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethyl carbamate

The compound 2-(7-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethyl carbamate is an intriguing molecule in the field of organic chemistry and pharmacology. Here are some fascinating details:

  • Structural Complexity: This compound exhibits a unique structure combining a benzoxazine ring with a carbamate moiety, showcasing the intriguing possibilities of heterocyclic chemistry.
  • Biological Significance: Benzoxazinones, including this compound, are known for their biological activities, including antibacterial, antifungal, and herbicidal properties, making them valuable in agricultural applications.
  • Research Applications: Due to its structural characteristics, it is often utilized in drug discovery and development, particularly in the synthesis of potential therapeutic agents.
  • Nitro Group: The presence of the nitro group is significant as it can enhance the reactivity of the compound and influence its biological activity, highlighting the intricate relationship between structure and function in chemical compounds.
  • Chemical Synthetic Routes: The synthesis of this compound typically involves a series of reaction steps, including nitrogen functionalization and carbamate formation, emphasizing the inventive strategies chemists employ to construct complex molecules.

As quoted in the research community, "The ability to manipulate molecular structures opens up new horizons in material science and pharmacology." The study of such compounds exemplifies how chemistry bridges the gap between fundamental science and practical innovation.

This compound not only serves as a subject of academic interest but also underlines the importance of interdisciplinary approaches in tackling real-world problems through chemistry.

Synonyms
BRN 1149753
21038-12-0
1H-2,3-BENZOXAZINE, 3,4-DIHYDRO-3-(2-CARBAMOYLOXYETHYL)-7-NITRO-
DTXSID80175245
3-(2-Carbamoyloxyethyl)-7-nitro-3,4-dihydro-1H-2,3-benzoxazine
1H-2,3-Benzoxazine, 3-(2-carbamoyloxyethyl)-3,4-dihydro-7-nitro-
RefChem:237267
DTXCID6097736