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Ketenimines

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Identification
Molecular formula
C10H8N2O4
CAS number
50306-13-1
IUPAC name
1-(6-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethanone
State
State
The compound exists as a solid at room temperature. It can be handled as a crystalline powder that is stable under standard conditions.
Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
322.00
Boiling point (Kelvin)
595.15
General information
Molecular weight
220.18g/mol
Molar mass
220.2110g/mol
Density
1.4100g/cm3
Appearence

1-(6-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethanone typically appears as a crystalline solid. The color of the compound can range from yellow to light brown due to the presence of a nitro group, which is often associated with yellowish hues in aromatic compounds.

Comment on solubility

Solubility of 1-(6-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethanone

The solubility of 1-(6-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethanone can be influenced by various factors, such as temperature, pH, and the presence of solvents. Understanding its solubility is essential for applications in chemical synthesis and pharmaceutical formulations. Here are the key points regarding its solubility:

  • Solvent Compatibility: This compound may show varying solubility in different solvents. Organic solvents such as dimethyl sulfoxide (DMSO) and ethanol are often good candidates to explore for solubilization.
  • Temperature Dependency: Generally, increasing the temperature can enhance solubility for many organic compounds, potentially leading to increased molecular motion and interactions with solvent molecules.
  • Influence of pH: The pH of the solvent can affect the ionization states of functional groups in the compound, thereby impacting its solubility. For example, a more acidic or basic environment may change the solubility profile drastically.
  • Hydrogen Bonding: The presence of functional groups such as nitro groups and ether linkages in this compound may facilitate or hinder solubility through hydrogen bonding interactions with solvent molecules.

In conclusion, the solubility of 1-(6-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethanone is a multifaceted attribute that would require empirical testing across various conditions to establish definitive solubility parameters. As always, it's paramount to approach solubility studies with a systematic experimental design for comprehensive insights.

Interesting facts

Interesting Facts About 1-(6-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethanone

This fascinating compound, 1-(6-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethanone, is a prime example of an aromatic nitro compound with intriguing structural features. Here are several key points that highlight its significance in both research and application:

  • Versatile Applications: This compound is used in various fields, particularly in the synthesis of agrochemicals and pharmaceuticals, owing to its unique reactivity and functional groups.
  • Potential Biological Activity: Nitro-substituted benzoxazines are often explored for their potential biological activities, including anti-inflammatory and anticancer properties, making this compound of high interest in medicinal chemistry.
  • Structural Intrigue: The presence of a benzoxazine structure confers a unique bicyclic arrangement, providing stability and contributing to its chemical properties. The bond between the nitro group and the benzoxazine ring can influence its reactivity significantly.
  • Synthetic Pathways: The compound can be synthesized through various creative methods, often involving condensation reactions, which enhance its accessibility in a laboratory setting.
  • Environmental Impact: As with many nitro compounds, the environmental behavior and potential toxicity of this compound must be studied carefully to ensure safe handling and application in agriculture and pharmaceuticals.

Researchers are continually exploring the extensive possibilities of compounds like 1-(6-nitro-1,4-dihydro-2,3-benzoxazin-3-yl)ethanone, reinforcing the essential role of chemical compounds in advancing technology and medicine. As noted in scientific literature, "the potential to modify and optimize these compounds can lead to breakthroughs in sustainable practices and novel therapeutic agents."


The dynamic nature of this compound exemplifies the ever-evolving world of organic chemistry, where each molecule holds secrets waiting to be unlocked by dedicated scientists and students.

Synonyms
21977-26-4
BRN 1219112
1H-2,3-BENZOXAZINE, 3,4-DIHYDRO-3-ACETYL-6-NITRO-
DTXSID10176386
3-Acetyl-6-nitro-3,4-dihydro-1H-2,3-benzoxazine
1H-2,3-Benzoxazine, 3-acetyl-3,4-dihydro-6-nitro-
RefChem:237268
DTXCID2098877
3-Acetyl-3,4-dihydro-6-nitro-1H-2,3-benzoxazine