Interesting facts
Exploring 7-isopropoxy-3-phenyl-chromen-4-one
7-isopropoxy-3-phenyl-chromen-4-one, a fascinating compound belonging to the class of flavonoids, has captured the interest of many scientists and researchers due to its diverse range of biological activities and applications. Here are some intriguing facts about this compound:
- Natural Sources: Many flavonoids, including derivatives like 7-isopropoxy-3-phenyl-chromen-4-one, can be found in various plants, where they play a crucial role in pigmentation and UV protection.
- Biological Activities: This compound exhibits potential anti-inflammatory, antioxidant, and anticancer properties, making it a subject of interest for drug discovery and medicinal chemistry.
- Pharmacological Potential: Due to its structural motifs, it is hypothesized that 7-isopropoxy-3-phenyl-chromen-4-one may interact with specific biological targets, leading to therapeutic effects against various diseases.
- Synthetic Accessibility: The synthesis of this compound is often studied to develop efficient pathways for creating flavonoid derivatives, highlighting its importance in organic chemistry.
- Research Applications: Researchers are actively investigating its properties in areas like cancer therapy, neuroprotection, and as a natural pesticide, illustrating the compound's versatility.
As quoted by renowned chemist, "The exploration of chemical compounds like 7-isopropoxy-3-phenyl-chromen-4-one not only enhances our understanding of nature but also opens doors to innovative solutions in health and agriculture."
This compound exemplifies the intersection of chemistry and biology, showcasing how understanding molecular structures can lead to significant advancements in science and medicine.
Synonyms
ipriflavone
35212-22-7
Osten
7-Isopropoxyisoflavone
Yambolap
Osteofix
Ipriflavona
Iprosten
7-Isopropoxy-3-phenyl-4H-1-benzopyran-4-one
Ipriflavonum
Osteoquine
Ostivone
3-phenyl-7-propan-2-yloxychromen-4-one
Ipriflavone [INN:JAN]
7-isopropoxy-3-phenyl-4H-chromen-4-one
Osten (TN)
Osteochin
3-phenyl-7-(propan-2-yloxy)-4H-chromen-4-one
TC 80
7-(1-Methylethoxy)-3-phenyl-4H-1-benzopyran-4-one
FL 113
FL-113
MLS000069470
7-isopropyloxy-isoflavone
MFCD00221719
SMR000059060
4H-1-Benzopyran-4-one, 7-(1-methylethoxy)-3-phenyl-
80BJ7WN25Z
DTXSID5040679
CHEBI:31719
NSC-755888
NCGC00024094-04
Quinogin
DTXCID3020679
Ipriflavone (Osteofix)
Iprivone
Ipriflavonum [INN-Latin]
Ipriflavona [INN-Spanish]
CAS-35212-22-7
CCRIS 1920
BRN 4754346
UNII-80BJ7WN25Z
Ipriflavon
(Ipriflavone)
Ipriflavone, INN
7-isopropoxy-isoflavone
Ipriflavone (Standard)
Ipriflavone (JAN/INN)
IPRIFLAVONE [MI]
Opera_ID_1176
IPRIFLAVONE [INN]
IPRIFLAVONE [JAN]
Ipriflavone (JP18/INN)
IPRIFLAVONE [VANDF]
Cambridge id 6663564
cid_3747
IPRIFLAVONE [MART.]
Oprea1_106310
Oprea1_275552
IPRIFLAVONE [WHO-DD]
MLS000759494
MLS001146879
MLS001424060
MLS006011644
SCHEMBL111472
7-isopropoxy-3-phenyl-chromone
CHEMBL165790
Ipriflavone, analytical standard
BDBM43662
HY-N0094R
SFBODOKJTYAUCM-UHFFFAOYSA-
FL113
HMS2051J15
HMS2234M05
HMS3371E17
HMS3393J15
HMS3656K19
HMS3715D04
TC-80
TN-39
HY-N0094
Tox21_111532
Tox21_113172
s2422
STL512460
AKOS003627375
Tox21_111532_1
Tox21_113172_1
AC-8130
CCG-100963
CS-6395
DB13618
FI07802
NC00213
NSC 755888
NCGC00018139-01
NCGC00018139-02
NCGC00018139-03
NCGC00018139-04
NCGC00018139-05
NCGC00018139-07
NCGC00018139-08
AS-12306
3-phenyl-7-propan-2-yloxy-chromen-4-one
DB-048754
I0669
NS00010326
SW197593-2
3-phenyl-7-propan-2-yloxy-1-benzopyran-4-one
D01338
D70301
AB00384280-21
SR-01000000042
Q1097778
SR-01000000042-2
7-Isopropoxy-3-phenyl-4H-1-benzopyran-4-one, 97%
BRD-K93618743-001-20-2
BRD-K93618743-001-21-0
F0196-0909
InChI=1/C18H16O3/c1-12(2)21-14-8-9-15-17(10-14)20-11-16(18(15)19)13-6-4-3-5-7-13/h3-12H,1-2H3
Solubility of 7-isopropoxy-3-phenyl-chromen-4-one
The solubility of 7-isopropoxy-3-phenyl-chromen-4-one (C18H16O3), a coumarin derivative, can be influenced by several physicochemical factors. Typically, the solubility of such compounds in various solvents can be categorized as follows:
Coumarins often exhibit limited solubility in polar solvents due to their relatively hydrophobic nature.
These compounds may dissolve more readily in non-polar solvents, as their hydrophobic characteristics align well with non-polar environments.
Intermediate solubility can be observed in mixed solvents, allowing for a balance between polar and non-polar characteristics.
Moreover, factors such as temperature and pH can further alter solubility:
In summary, while 7-isopropoxy-3-phenyl-chromen-4-one displays selective solubility profiles, it is essential to consider the choice of solvent and environmental conditions to optimize its solubility for various applications. As the saying goes, “like dissolves like,” emphasizing the importance of matching the solute's properties with those of the solvent for effective dissolution.