Interesting facts
Interesting Facts about 2-Phenylchroman-4-one
2-Phenylchroman-4-one, also known in certain circles as a specific flavonoid derivative, has garnered attention for its intriguing properties and potential applications. Below are some engaging aspects of this compound:
- Natural Origins: This compound is part of a larger family of flavonoids, which are commonly found in plants and play a crucial role in plant coloration and health. Flavonoids are renowned for their antioxidant properties, contributing to the plant's defense mechanisms.
- Biological Activity: 2-Phenylchroman-4-one has been studied for its potential health benefits. Some research suggests it may exhibit anti-inflammatory and anticancer properties, making it a compound of interest in pharmaceutical development.
- Structural Nuances: The structural makeup of this compound includes a chroman ring fused with a phenyl group, which imparts unique chemical properties. This fusion enhances reactivity and can influence how the compound interacts with other molecules.
- Research Applications: Its unique structure encourages investigations into its applications within the fields of organic synthesis and medicinal chemistry. Scientists are exploring how modifications to its structure can enhance its therapeutic potential.
- Historical Context: Flavonoids, including derivatives like 2-phenylchroman-4-one, have been utilized in traditional medicine for centuries. They have roots in ancient herbal practices, highlighting the longstanding human fascination with plant-derived compounds.
In summary, 2-phenylchroman-4-one is not just a chemical entity; it embodies a blend of traditional knowledge and modern scientific inquiry. As research continues, this compound may unveil even more secrets about its role in health and disease management.
Synonyms
FLAVANONE
487-26-3
2-Phenylchroman-4-one
2,3-Dihydroflavone
4-Flavanone
2,3-Dihydro-2-phenyl-4H-1-benzopyran-4-one
NSC-50393
4H-1-Benzopyran-4-one, 2,3-dihydro-2-phenyl-
2-Phenyl-2,3-dihydro-4H-chromen-4-one
EINECS 207-654-8
UNII-WX22P730FB
NSC 50393
BRN 0183227
CHEBI:5070
WX22P730FB
DL-FLAVANONE
2-phenyl-2,3-dihydrochromen-4-one
DTXSID9022318
ZONYXWQDUYMKFB-UHFFFAOYSA-
5-17-10-00480 (Beilstein Handbook Reference)
PROPAFENONE HYDROCHLORIDE IMPURITY H [EP IMPURITY]
(+-)-flavanone
PROPAFENONE HYDROCHLORIDE IMPURITY H (EP IMPURITY)
a flavanone
phenylchroman-4-one
DTXCID302318
flavanone, (+-)-
inchi=1/c15h12o2/c16-13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-9,15h,10h2
zonyxwqduymkfb-uhfffaoysa-n
2-Phenyl-4-chromanone
Flavanone-d5
2,3-Dihydro-2-phenyl-4H-benzopyran-4-one
2-Phenylchromanone
MFCD00006841
(+/-)-flavanone
MLS002667384
CHEMBL274318
FLAVANONE, (+/-)-
NSC50393
(2RS)-2-Phenyl-2,3-dihydro-4H-1-benzopyran-4-one
FLAVANONE (3,3-D2)
SMR001306759
2-Phenyl-chroman-4-one
Propafenone IMpurity H (EP/BP/USP)
2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one
flavan-4-one
Propafenone Hydrochloride Imp. H (EP); Propafenone Imp. H (EP); (2RS)-2-Phenyl-2,3-dihydro-4H-1-benzopyran-4-one; Propafenone Hydrochloride Impurity H; Propafenone Impurity H
Flavanone, 98%
2-phenyl-2
Spectrum_000081
SpecPlus_000724
Spectrum2_000205
Spectrum3_000174
Spectrum4_001646
Spectrum5_000491
Flavone, 2,3-dihydro-
(2R)-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one
Oprea1_401736
SCHEMBL19745
BSPBio_001667
GTPL408
KBioGR_002111
KBioSS_000501
SPECTRUM200343
MLS002207195
DivK1c_006820
SPBio_000189
MEGxp0_001684
ACon1_002246
KBio1_001764
KBio2_000501
KBio2_003069
KBio2_005637
KBio3_001167
HY-N7128
WFA19691
BBL027613
BDBM50051358
CCG-21177
s3679
STL373060
AKOS000120276
AKOS016040110
FF23297
NCGC00095802-01
NCGC00095802-02
NCGC00095802-03
NCGC00095802-05
AS-48159
DA-53215
NCI60_004213
SY049235
2-Phenyl-2,3-dihydro-4H-chromen-4-one #
CS-0030762
EU-0012871
F0255
NS00007587
4H-1-Benzopyran-4-one,3-dihydro-2-phenyl-
EN300-17915
C00766
F19539
L000786
SR-01000500943
F4C11F5A-DFFA-4E0E-BCC9-2FD60204B2DD
SR-01000500943-1
BRD-A07824748-001-02-6
BRD-A07824748-001-03-4
Q27077305
Z57085783
2,3-Dihydro-2-phenyl-4H-1-benzopyran-4-one;2,3-Dihydroflavone
Solubility of 2-phenylchroman-4-one
2-phenylchroman-4-one has a unique solubility profile that can be influenced by various factors. This compound is generally characterized as:
In terms of solubility behavior:
It is often noted that, as with many organic compounds, the solubility is greatly affected by the “like dissolves like” principle, meaning nonpolar compounds will favorably dissolve in nonpolar solvents. Therefore, to effectively utilize 2-phenylchroman-4-one in practical applications, it's essential to select the appropriate solvent based on its solubility characteristics.