Interesting facts
Exploring 2-Methoxy-2-Methyl-4-Phenyl-3,4-Dihydropyrano[3,2-c]chromen-5-one
This compound, known for its unique structure and properties, occupies an interesting niche in the world of organic chemistry. Here are some fascinating insights:
- Natural Products: 2-methoxy-2-methyl-4-phenyl-3,4-dihydropyrano[3,2-c]chromen-5-one is often associated with the chemical family of natural products, particularly flavonoids and chromenes. These compounds are known for their diverse biological activities.
- Pharmacological Potential: Research indicates that similar structures have exhibited a range of pharmacological properties, including anti-inflammatory, antioxidant, and anticancer activities. This could suggest a potential role in drug development.
- Synthetic Interest: The synthesis of this compound can be a subject of intrigue in organic chemistry. Its complex structure offers a great opportunity to explore various synthetic pathways, including multi-step reactions that highlight the creativity of synthetic chemists.
- Varied Applications: Besides medicinal chemistry, compounds of this nature can also be studied in the fields of material science and agricultural chemistry. They may serve as bioactive agents or contribute to innovative material formulations.
As we delve deeper into the complexities of such compounds, we can appreciate their multifaceted roles in both nature and synthetic applications. The study of 2-methoxy-2-methyl-4-phenyl-3,4-dihydropyrano[3,2-c]chromen-5-one not only enriches our understanding of chemical interactions but also paves the way for novel research avenues.
As one researcher put it, "The beauty of chemistry lies in its ability to create unexpected connections and solutions." Exploring this compound exemplifies this sentiment perfectly.
Synonyms
Cyclocoumarol
CYCLOCUMAROL
518-20-7
Pyranocumarin
Pyranocumarin [German]
2-methoxy-2-methyl-4-phenyl-3,4-dihydropyrano[3,2-c]chromen-5-one
EINECS 208-248-3
UNII-725P8AW50M
anticoagulant No. 63
725P8AW50M
CYCLOCUMAROL [MI]
DTXSID60862101
2-Methyl-2-methoxy-4-phenyl-3,4-dihydro-pyrano-(3,2-c)-cumarin [German]
2-Methyl-2-methoxy-4-phenyl-3,4-dihydro-pyrano-(3,2-c)-cumarin
methopyranorin
3,4-(2'-Methyl-2'-methoxy-4'-phenyl)dihydropyranocoumarin
2-methoxy-2-methyl-4-phenyl-3,4-dihydropyrano(3,2-c)chromen-5-one
DTXCID10810915
3,4-Dihydro-2-methoxy-2-methyl-4-phenyl-2H,5H-pyrano-(3,2-c)(1)-benzopyran-5-one
208-248-3
zgfasekbkwvcgp-uhfffaoysa-n
Pyranocoumarin
Cumopyran
Cumopyrin
Methanopyranorin
Anticoagulans 63
Compound 63 link
BL 5
3,4-Dihydro-2-methoxy-2-methyl-4-phenyl-2H,5H-pyrano(3,2-c)(1)benzopyran-5-one
2H,5H-Pyrano(3,2-c)(1)benzopyran-5-one, 3,4-dihydro-2-methoxy-2-methyl-4-phenyl-
2H,5H-Pyrano[3,2-c][1]benzopyran-5-one, 3,4-dihydro-2-methoxy-2-methyl-4-phenyl-
starbld0009647
Cyclocoumarol [INN:BAN]
SCHEMBL38087
CHEMBL2104144
CHEBI:135368
3,4-Dihydro-2-methoxy-2-methyl-4-phenylpyrano(3,2-c)chromen-5-one
NCGC00166195-01
2H-Pyran-5-carboxylic acid, 3,4-dihydro-6-(o-hydroxyphenyl)-2-methoxy-2-methyl-4-phenyl-, delta-lactone
NS00044150
Pyranocoumarin, PESTANAL(R), analytical standard
SR-01000883723
SR-01000883723-1
Q27266024
2-Methoxy-2-methyl-4-phenyl-3,4-dihydro-2H,5H-pyrano[3,2-c]chromen-5-one #
2H-Pyran-5-carboxylic acid, 3,4-dihydro-6-(o-hydroxyphenyl)-2-methoxy-2-methyl-4-phenyl-, .delta.-lactone
Solubility of 2-methoxy-2-methyl-4-phenyl-3,4-dihydropyrano[3,2-c]chromen-5-one
The solubility of 2-methoxy-2-methyl-4-phenyl-3,4-dihydropyrano[3,2-c]chromen-5-one is influenced by its complex structure and functional groups present within the molecule. This compound displays characteristics typical of many organic compounds, and its solubility can be described as follows:
In summary, one can state that "solubility is a key factor in determining the usability of a compound in different chemical contexts." The solubility of 2-methoxy-2-methyl-4-phenyl-3,4-dihydropyrano[3,2-c]chromen-5-one is predominantly favorable in organic solvents, making it an interesting candidate for various chemical applications.