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7-ethoxyphenoxazin-3-one

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Identification
Molecular formula
C14H11NO3
CAS number
2431-16-9
IUPAC name
7-ethoxyphenoxazin-3-one
State
State

At room temperature, 7-ethoxyphenoxazin-3-one is in a solid state. It is typically handled as a solid powder.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
438.00
Boiling point (Kelvin)
711.15
General information
Molecular weight
241.25g/mol
Molar mass
241.2500g/mol
Density
0.9874g/cm3
Appearence

The compound typically appears as a red solid. It is characterized by its vibrant color and is usually available in a crystalline form.

Comment on solubility

Solubility of 7-Ethoxyphenoxazin-3-one

When considering the solubility of 7-ethoxyphenoxazin-3-one (C14H11NO3), several factors come into play:

  • Polarity: This compound contains both aromatic and ether functionalities, suggesting a moderate polarity which may affect its solubility in various solvents.
  • Solvent Compatibility: Typically, compounds like 7-ethoxyphenoxazin-3-one tend to be more soluble in organic solvents such as ethanol, methanol, and acetone, rather than in polar solvents like water.
  • Temperature Dependence: The solubility may increase with temperature, as is common with many organic compounds, potentially allowing for easier dissolution in warmer conditions.

In conclusion, while precise solubility data for 7-ethoxyphenoxazin-3-one is limited, its chemical structure suggests it may exhibit characteristics typical of similar organic compounds, and thus could be more soluble in non-polar or less polar solvents than in water.

Interesting facts

Interesting Facts about 7-Ethoxyphenoxazin-3-one

7-Ethoxyphenoxazin-3-one is an intriguing compound that belongs to the phenoxazine class of compounds, notable for their diverse applications in various chemical and biological fields. Here are some captivating aspects of this compound:

  • Fluorescent Properties: This compound is recognized for its potential fluorescent properties, making it a valuable tool in biological imaging and detection.
  • Biological Applications: It has garnered interest in medicinal chemistry, particularly for its possible use in developing photodynamic therapy agents to treat cancer.
  • Electrochemical Activity: 7-ethoxyphenoxazin-3-one exhibits interesting electrochemical behaviors, opening avenues for its use in organic electronics and sensors.
  • Substituent Influence: The ethoxy group at the 7-position plays a crucial role in modulating the compound’s physicochemical properties, such as solubility and reactivity.
  • Synthetic Routes: Various synthetic methodologies are employed to produce this compound, including multi-step reactions that highlight the creativity and complexity inherent in organic synthesis.

In conclusion, the multifaceted nature of 7-ethoxyphenoxazin-3-one showcases its potential as an important compound in both academic and industrial research. As research continues, the scope of this compound's applications may extend even further, prompting excitement in the scientific community.

Synonyms
7-Ethoxyresorufin
5725-91-7
7-Ethoxy-3H-phenoxazin-3-one
Resorufin ethyl ether
ETHOXYRESORUFIN
7-ethoxy resorufin
7-Ethoxyphenoxazone
7-ethoxyphenoxazin-3-one
3H-Phenoxazin-3-one, 7-ethoxy-
CHEBI:34480
O-ETHYLRESORUFIN
59AF853SW7
DTXSID90205860
MFCD00037661
O7-Ethylresorufin
Resorufinethyl ether
7-ethoxy-3-phenoxazinone
SCHEMBL104497
UNII-59AF853SW7
7-ER
CHEMBL1080002
BDBM21360
DTXCID20128351
CRCWUBLTFGOMDD-UHFFFAOYSA-N
HY-D0145
STK299139
AKOS005428988
ER22912
AS-59402
CS-0010054
NS00115885
D97845
7-Ethoxy-3H-phenoxazin-3-one;7-O-Ethoxyresorufin
Q27116097