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6-Nitrosochromen-2-one

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Identification
Molecular formula
C9H5NO3
CAS number
55956-09-1
IUPAC name
6-nitrosochromen-2-one
State
State

At room temperature, 6-Nitrosochromen-2-one remains in a solid state. It typically requires higher temperatures to undergo phase transition to liquid, based on its melting point.

Melting point (Celsius)
116.00
Melting point (Kelvin)
389.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
177.15g/mol
Molar mass
177.1530g/mol
Density
1.4960g/cm3
Appearence

6-Nitrosochromen-2-one typically presents as a crystalline solid, characterized by its distinct coloration and crystalline structure. This compound may appear in various shades depending on its preparation and purity.

Comment on solubility

Solubility of 6-Nitrosochromen-2-one

6-Nitrosochromen-2-one, with the chemical formula C9H5NO3, presents intriguing solubility characteristics that are important to understand in both practical applications and theoretical studies. Here are some key points regarding its solubility:

  • Polar vs Non-Polar Solvents: The presence of the nitroso and carbonyl functional groups contributes to its polar nature, allowing it to be soluble in polar solvents such as water and alcohol.
  • Hydrogen Bonding: The functional groups can engage in hydrogen bonding, which enhances solubility in solvents that can act as hydrogen bond donors.
  • Solubility Limits: While 6-nitrosochromen-2-one exhibits some degree of solubility in organic solvents, exact solubility values may vary. It is recommended to consult specific literature for quantitative data.
  • Crystallization: Due to its aromatic structure, 6-nitrosochromen-2-one can also form crystals in certain conditions. This can affect its solubility as temperature varies.

In summary, the solubility of 6-nitrosochromen-2-one is influenced by its functional groups and aromatic nature. Understanding these factors can help in predicting its behavior in various chemical environments, making it a compound of interest in organic chemistry.

Interesting facts

Interesting Facts about 6-Nitrosochromen-2-one

6-Nitrosochromen-2-one, a fascinating compound in the realm of organic chemistry, belongs to the broader class of chromones. Here are some intriguing points regarding its structure and significance:

  • Unique Structure: The compound features a nitroso group attached to the chromone skeleton, which plays a critical role in its reactivity and biological properties.
  • Biological Relevance: Compounds related to chromones, including 6-nitrosochromen-2-one, are known for their diverse biological activities such as anti-inflammatory, antioxidant, and antimicrobial effects. They are often studied for potential pharmaceutical applications.
  • Synthetic Pathways: The synthesis of 6-nitrosochromen-2-one can be achieved through various methods, including nitration reactions. These reactions are essential to organic synthesis and contribute to its development.
  • Research Potential: Due to its distinct functional groups, 6-nitrosochromen-2-one is a subject of ongoing research, particularly in fields such as medicinal chemistry and material science.
  • Chromone Derivatives: This compound belongs to a broader category of chromone derivatives that are not only significant in medicinal chemistry but also demonstrate interesting photochemical properties.

As you explore the depths of organic chemistry, 6-nitrosochromen-2-one serves as a prime example of how slight modifications in molecular structure can lead to significant changes in chemical and biological behavior. Its study not only enriches our understanding of chromones but also enhances potential therapeutic avenues.

"The beauty of chemistry lies in the complexity and simplicity of its structures and reactions." - An avid chemist

Synonyms
6-Nitroso-1,2-benzopyrone
130506-22-8
6-nitroso-2H-chromen-2-one
6-nitrosochromen-2-one
2H-1-Benzopyran-2-one, 6-nitroso-
6-NO2BP
DTXSID90156580
6-Nitrosocoumarin
NOBP
Lopac-N-8403
6-NOBP
Lopac0_000869
SCHEMBL792923
CHEMBL1255659
DTXCID8079071
HMS3262N19
Tox21_500869
AKOS006271903
CCG-204951
LP00869
SDCCGSBI-0050844.P002
NCGC00015753-01
NCGC00015753-02
NCGC00015753-03
NCGC00015753-04
NCGC00094193-01
NCGC00094193-02
NCGC00261554-01
AS-85538
PD015149
DB-350613
EU-0100869
N 8403
SR-01000076033
SR-01000076033-1
6-Nitroso-1,2-benzopyrone, ADP-ribosyltransferase inhibitor