Skip to main content

9H-Xanthen-9-one

ADVERTISEMENT
Identification
Molecular formula
C13H8O2
CAS number
90-47-1
IUPAC name
xanthen-9-one
State
State

At room temperature, 9H-Xanthen-9-one is typically found in a solid state. It is stable and non-volatile under normal conditions.

Melting point (Celsius)
172.00
Melting point (Kelvin)
445.00
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.00
General information
Molecular weight
196.21g/mol
Molar mass
196.2090g/mol
Density
1.3367g/cm3
Appearence

9H-Xanthen-9-one is a pale yellow crystalline solid. It exhibits fluorescence under ultraviolet light and is often used as a dye or in dye synthesis due to its bright color properties.

Comment on solubility

Solubility of Xanthen-9-one

Xanthen-9-one, with the chemical formula C13H10O, exhibits interesting solubility characteristics that can be noteworthy for its applications in various fields.

In terms of solvent interactions, xanthen-9-one displays differing solubility behavior in various media:

  • Polar Solvents: It has moderate solubility in polar solvents such as water and alcohols, primarily due to the presence of its functional groups.
  • Nonpolar Solvents: Conversely, xanthen-9-one is more soluble in nonpolar solvents like toluene and benzene, reflecting its hydrophobic character.
  • Temperature Dependence: As with many organic compounds, its solubility can increase with temperature, which can be advantageous in processes requiring dissolution before chemical reactions.

In essence, when considering the solubility of xanthen-9-one, it is essential to keep in mind:

  • The solvent type and polarity
  • The concentration of the solution
  • The temperature at which the dissolution occurs

Ultimately, understanding the solubility of xanthen-9-one is vital for optimizing its use in research and application settings, reflecting the profound relationship between chemical structure and solvent compatibility.

Interesting facts

Interesting Facts about Xanthen-9-one

Xanthen-9-one is a fascinating compound that belongs to the class of xanthones and holds significant importance in various fields, particularly in organic chemistry and biochemistry. Here are some captivating details about this compound:

  • Structure and Isomerism: Xanthen-9-one features a unique heterocyclic structure consisting of three fused rings, providing it with distinct chemical properties and reactivity. Its structure also allows for several isomeric forms, which can exhibit diverse biological activities.
  • Biological Relevance: Compounds related to xanthen-9-one have shown promising results in pharmacological studies. They are often investigated for their potential medicinal properties including anti-inflammatory, antibacterial, and even anticancer effects.
  • Fluorescent Properties: One of the intriguing characteristics of this compound is its ability to fluoresce. This makes xanthen-9-one and its derivatives useful in various applications such as fluorescence microscopy and as fluorescent markers in biochemical assays.
  • Synthesis: Xanthen-9-one can be synthesized through various methods, including cyclization reactions. This versatility in synthetic routes allows chemists to explore its derivatives easily, which can lead to the discovery of new compounds with enhanced properties.
  • Analytical Applications: The unique properties of xanthen-9-one enable it to be used in analytical chemistry, particularly in high-performance liquid chromatography (HPLC) for the detection and quantification of various substances.

In summary, xanthen-9-one represents a rich area of study within the realm of chemical sciences, with its unique structure enabling a variety of applications. As researchers continue to explore this compound, it's evident that xanthen-9-one will remain an essential subject of interest for years to come.

Synonyms
XANTHONE
9H-Xanthen-9-one
90-47-1
Xanthen-9-one
9-Xanthenone
Benzophenone oxide
9-Oxoxanthene
Xanthenone
Genicide
9-Xanthone
Diphenylene ketone oxide
Dibenzo-gamma-pyrone
Xanthene, 9-oxo-
9H-Xanthene, 9-oxo-
Caswell No. 905
Dibenzo-.gamma.-pyrone
NSC 14978
diphenyline ketone oxide
EINECS 201-997-7
UNII-9749WEV0CA
MFCD00005060
EPA Pesticide Chemical Code 086503
9749WEV0CA
DTXSID6021795
CHEBI:37647
AI3-00077
XANTHONE [MI]
NSC-14978
XANTHONE [USP-RS]
CHEMBL186784
DTXCID201795
E 6
NSC14978
XANTHONE (USP-RS)
Dibenzo(b,e)pyran-10-one
Dibenzo[b,e]pyran-10-one
9Oxoxanthene
9Xanthenone
Xanthen9one
9Xanthone
Dibenzo-g-pyrone
Dibenzogammapyrone
9HXanthen9one
xanthene-9-one
Xanthene, 9oxo
Dibenzo-I3-pyrone
9HXanthene, 9oxo
Xanthone (Genicide)
Xanthone (Standard)
Xanthone, 97%
ST024714
Spectrum2_000052
Spectrum3_001884
SCHEMBL41161
BSPBio_003388
SPECTRUM200523
MLS002207109
SPBio_000203
ghl.PD_Mitscher_leg0.1212
HY-N0126R
KBio3_002891
WLN: T C666 BO IVJ
HMS3651G22
BCP21155
HY-N0126
STR05546
Tox21_301151
BDBM50155411
CCG-38356
s2372
STK372481
AKOS001213782
FX29267
SDCCGMLS-0066462.P001
CAS-90-47-1
NCGC00095484-01
NCGC00095484-02
NCGC00095484-03
NCGC00255049-01
DA-68731
SMR000112239
SY017687
CS-0007833
NS00039360
SW219800-1
X0005
EN300-20176
C22599
F15407
AC-907/21098006
Q421789
SR-05000002437
SR-05000002437-1
BRD-K27135764-001-08-7
F8889-9282
Z104477176
Xanthone, United States Pharmacopeia (USP) Reference Standard