Interesting facts
Exploring Ethyl 2-(4-oxo-2-phenyl-chromen-7-yl)oxyacetate
Ethyl 2-(4-oxo-2-phenyl-chromen-7-yl)oxyacetate is a fascinating compound with intriguing properties and potential applications. This compound belongs to the family of chromenone derivatives, which are well-known for their diverse biological activities. Here are some interesting facts:
- Bioactivity: Compounds like ethyl 2-(4-oxo-2-phenyl-chromen-7-yl)oxyacetate are often studied for their antioxidant properties. Research has indicated that they may help in combating oxidative stress in biological systems.
- Pharmacological Potential: The structural features of this compound suggest it may have valuable pharmacological properties, including anti-inflammatory and anticancer activities. Many chromenones are explored as potential leads for drug development.
- Synthesis: The synthesis of such compounds can be a delightful challenge for chemists, often involving creative organic reactions that highlight the principles of modern synthetic chemistry.
- Applications: Beyond their medicinal potential, derivatives of chromenones can be utilized in various fields, including agrochemicals and material sciences, due to their versatility and functional properties.
- Structure-Activity Relationship: Studying the structure-activity relationship (SAR) of this compound can provide critical insights into how modifications to its structure influence biological activity, enabling the design of more effective derivatives.
In conclusion, ethyl 2-(4-oxo-2-phenyl-chromen-7-yl)oxyacetate is more than just a chemical compound; it's a promising contender in the world of drug discovery and bioactive materials. With its unique properties, this compound invites further research and exploration in various scientific domains.
Synonyms
Efloxate
119-41-5
Angorlisin
Coril
Efloxato
NSC-758891
CZU6V3902K
Flacethyle
Corosanin
DTXSID3048736
Oxiflavil
Oxyflavil
Recordil
ethyl 2-((4-oxo-2-phenyl-4H-chromen-7-yl)oxy)acetate
NCGC00182622-01
NCGC00182622-02
Domucor
Efloxatum
Ethyl-((4-oxo-2-phenyl-4H-1-benzopyran-7-yl)oxy) acetate
Dilatan kore
Eflossato [DCIT]
DTXCID0028662
Ethyl 7-hydroxyflavone
Eflossato
Efloxate [INN:JAN]
Ethyl 7-flavonoxyacetate
Efloxato [INN-Spanish]
Ethyl flavone-7-oxyacetate
Flavone-7-ethyl-oxyacetate
Ethyl flavon-7-yloxyacetate
CAS-119-41-5
7-Flavone ethyl hydroxyacetate
CCRIS 5253
RE 1-0185
7-Flavonoxyacetic acid ethyl ester
7-alpha-(Acetoxyethane)-oxyflavone
EINECS 204-321-9
ethyl 2-[(4-oxo-2-phenyl-4H-chromen-7-yl)oxy]acetate
REC 1-0185
BRN 0313027
UNII-CZU6V3902K
Efloxate (Standard)
Efloxate (JAN/INN)
EFLOXATE [INN]
EFLOXATE [JAN]
EFLOXATE [MI]
Maybridge3_003026
((4-Oxo-2-phenyl-4H-1-benzopyran-7-yl)oxy)acetic acid ethyl ester
EFLOXATE [MART.]
EFLOXATE [WHO-DD]
ethyl 2-(4-oxo-2-phenylchromen-7-yl)oxyacetate
Oprea1_663744
4-18-00-00695 (Beilstein Handbook Reference)
MLS000859001
SCHEMBL309159
CHEMBL1349073
CHEBI:31531
HY-B0930R
ZVXBAHLOGZCFTP-UHFFFAOYSA-N
HMS1439J12
HMS2787P19
HMS3264O09
Pharmakon1600-01504518
AAA11941
HY-B0930
Tox21_113177
Tox21_113178
NSC758891
AKOS030526077
CCG-213948
CS-4399
DB13333
NSC 758891
ACETIC ACID, ((4-OXO-2-PHENYL-4H-1-BENZOPYRAN-7-YL)OXY)-, ETHYL ESTER
IDI1_014413
NCGC00182622-03
DA-73019
MS-24824
SMR000459180
SBI-0207066.P001
NS00001790
D01135
F85196
AB00643675_07
Q962269
SR-01000760674
SR-01000760674-2
BRD-K55166090-001-03-3
BRD-K55166090-001-07-4
BRD-K55166090-001-09-0
Solubility of Ethyl 2-(4-oxo-2-phenyl-chromen-7-yl)oxyacetate
The solubility of ethyl 2-(4-oxo-2-phenyl-chromen-7-yl)oxyacetate (C18H18O4) can be an intriguing aspect to investigate, particularly considering its structure and functional groups.
Generally, the solubility of organic compounds like this one is influenced by several factors:
For ethyl 2-(4-oxo-2-phenyl-chromen-7-yl)oxyacetate, it may show:
In conclusion, the solubility profile of this compound is expected to reflect a balance between its polar and non-polar characteristics, making it essential to assess specific solvent interactions for practical applications.