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Flavone

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Identification
Molecular formula
C15H10O2
CAS number
525-82-6
IUPAC name
2-phenylchromen-4-one
State
State

Flavone is a solid at room temperature, present as a stable crystalline powder.

Melting point (Celsius)
98.00
Melting point (Kelvin)
371.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
222.24g/mol
Molar mass
222.2430g/mol
Density
1.2577g/cm3
Appearence

Flavone appears as a pale yellow solid with a crystalline texture. It is a component of certain plant pigments and imparts a yellow hue.

Comment on solubility

Solubility of 2-phenylchromen-4-one

2-phenylchromen-4-one, also known as flavone, exhibits interesting solubility characteristics which can vary depending on the medium. Here are some key points to consider:

  • Solvent Dependence: This compound is known to be soluble in organic solvents such as ethanol, methanol, and acetone, making it suitable for various applications in organic synthesis.
  • Water Solubility: One of the main features of flavone is its relatively low solubility in water, usually yielding only minimal amounts, which can limit its application in aqueous environments.
  • Temperature Influence: Increasing the temperature typically enhances the solubility of 2-phenylchromen-4-one in organic solutions, highlighting the impact of thermal energy on the dissolution process.

Overall, the solubility of 2-phenylchromen-4-one is a crucial factor for its utility in various fields, including pharmacology and organic chemistry. As with many compounds, understanding its solubility profile can open new avenues for research and application.

Interesting facts

Interesting Facts about 2-Phenylchromen-4-one

2-Phenylchromen-4-one, also known as a type of flavonoid, is a fascinating compound that boasts a variety of intriguing properties. Here are some noteworthy aspects:

  • Natural Occurrence: This compound is often found in various plants, contributing to their vibrant colors and potential health benefits. Flavonoids, like 2-phenylchromen-4-one, are known for their presence in fruits, vegetables, and herbs.
  • Biological Activity: Research has shown that compounds in the flavonoid family can exhibit a range of biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. These effects make 2-phenylchromen-4-one of interest in medicinal chemistry.
  • Structure and Reactivity: The unique structure of 2-phenylchromen-4-one allows it to engage in various chemical reactions, making it a valuable target for synthetic chemists aiming to develop new compounds with enhanced properties.
  • Potential Applications: Due to its biological activities, 2-phenylchromen-4-one is being studied for potential applications in pharmaceuticals, particularly in designing drugs to combat oxidative stress and related diseases.
  • Flavor and Fragrance: In addition to its medicinal properties, this compound can also contribute to the flavor and aroma of certain foods, enhancing our culinary experiences.

As scientists continue to explore 2-phenylchromen-4-one, numerous opportunities arise in both academic research and practical applications. Its rich history in traditional medicine paired with cutting-edge research may pave the way for innovative treatments and products that benefit health and well-being.

Synonyms
FLAVONE
2-Phenyl-4H-chromen-4-one
2-Phenylchromone
2-Phenyl-4-chromone
Asmacoril
Chromocor
2-phenylchromen-4-one
Cromaril
2-Phenyl-4H-1-benzopyran-4-one
2-Phenyl-4-benzopyron
4H-1-Benzopyran-4-one, 2-phenyl-
Phenylchromone
Cromarile
2-Phenyl-gamma-benzopyrone
Flavon
2-Phenylbenzopyran-4-one
2-Phenyl-4H-benzopyran-4-one
2-Phenyl-.gamma.-benzopyrone
Flavone (VAN)
2-Phenyl-4H-chromen-4-on
NSC 19028
NSC-19028
CCRIS 4288
2-phenyl-1,4-benzopyrone
EINECS 208-383-8
UNII-S2V45N7G3B
BRN 0157598
S2V45N7G3B
DTXSID2022048
CHEBI:42491
FLAVONE [MI]
2-phenyl-1-benzopyran-4-one
DTXCID602048
5-17-10-00552 (Beilstein Handbook Reference)
Flavone (VAN) (8CI)
CHEBI:24043
208-383-8
inchi=1/c15h10o2/c16-13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-10
vhbffqkbgnrlfz-uhfffaoysa-n
525-82-6
2-Phenyl-chromen-4-one
MFCD00006825
NSC19028
MLS002638647
CHEMBL275638
NCGC00090962-05
CAS-525-82-6
FLN
SMR000112315
Flavone, Flavone
4hki
2-phenyl-4H-chromone
Maybridge3_005286
bmse000945
CBiol_000263
SCHEMBL18879
GTPL409
MLS002177804
MLS002473400
2-Phenylbenzo[b]pyran-4-one
BIDD:ER0515
MEGxp0_001685
2-Phenyl-4H-chromen-4-one #
ACon1_000055
HMS1446A06
HMS2269O06
HMS3604K19
HY-N2424
Tox21_202987
Tox21_400059
BDBM50028962
ICCB2_000263
LMPK12110097
s3967
STK164205
AKOS000603572
CCG-214679
DB07776
FF52488
IDI1_016673
NCGC00090962-01
NCGC00090962-02
NCGC00090962-03
NCGC00090962-04
NCGC00090962-06
NCGC00168837-01
NCGC00260532-01
AC-35144
AS-58464
SY012830
DB-052142
CS-0022637
F0015
NS00007856
C10043
AH-357/03404044
EN300-18246169
L001213
CU-00000000060-1
Q2742033
BRD-K86741145-001-01-5
6CC153EB-39A6-42FC-BE96-C8BF1D585E27
2-Phenyl-4H-1-benzopyran-4-one;2-Phenyl-4H-chromen-4-one
11091-19-3