Interesting facts
Exploring 8-hydroxy-3-methyl-isochroman-1-one
8-hydroxy-3-methyl-isochroman-1-one, often referred to simply as a flavonoid compound, is intriguing not only for its structural uniqueness but also for its diverse biological activities. Here are some captivating facts about this compound:
- Active Components: This compound belongs to a group of phenolic compounds known as isochromans, which are recognized for their noteworthy biological and medicinal properties.
- Potential Health Benefits: Research has suggested that flavonoids may exhibit antioxidant, anti-inflammatory, and anticancer properties. These effects are largely attributed to their ability to scavenge free radicals and modulate various cellular pathways.
- Natural Sources: 8-hydroxy-3-methyl-isochroman-1-one is often isolated from plants used in traditional medicines, showcasing their role in natural health remedies and highlighting the importance of biodiversity in pharmaceutical discoveries.
- Synthetic Pathways: Synthetic chemistry has played a vital role in producing this compound, allowing scientists to explore various methods of synthesis and modification that could enhance its efficacy for potential therapeutic applications.
- Applications in Research: The compound is a subject of interest in various fields, including chemistry, pharmacology, and environmental science, due to its properties that can influence biochemical pathways.
As Dr. Jane Goodwin aptly put it, "Nature has a way of producing compounds that can significantly alter human health." This is precisely why compounds like 8-hydroxy-3-methyl-isochroman-1-one are of paramount interest in ongoing scientific research. With further studies, we may unlock new avenues for drug development and health benefit applications!
Synonyms
Mellein
Ochracin
17397-85-2
8-hydroxy-3-methyl-3,4-dihydroisochromen-1-one
CHEBI:38760
DTXSID60891794
DTXCID601001441
Y30Y67M5SV
1200-93-7
3,4-Dihydro-8-hydroxy-3-methylisocoumarin
1H-2-Benzopyran-1-one, 3,4-dihydro-8-hydroxy-3-methyl-
8-hydroxy-3-methylisochroman-1-one
(S)-(+)-Ochracin
AO-2
8-hydroxy-3-methyl-3,4-dihydro-1H-2-benzopyran-1-one
(+/-)-MELLEIN
8-HYDROXY-3-METHYL-ISOCHROMAN-1-ONE
ISOCOUMARIN, 3,4-DIHYDRO-8-HYDROXY-3-METHYL-
3,4-dihydro-8-hydroxy-3-methyl-1H-2-benzopyran-1-one
CHEMBL226090
8-Hydroxy-3-methyl-3,4-dihydro-1H-isochromen-1-one
3,4-Dihydro-8-hydroxy-3-methyl-(1H)-2-benzopyran-1-one
Antibiotic AO-2
Antibiotic BV-1
BV-1
starbld0003745
(.+/-.)-Mellein
ALM-9
orb1679950
SCHEMBL1230955
(R)-3,4-Dihydro-8-hydroxy-3-methyl-1H-2-benzopyran-1-one; (R)-Mellein
SCHEMBL13925643
BAA20093
SAA39785
BDBM50208249
( inverted exclamation markA)-Mellein
AKOS006228659
TS-10233
3-methyl-8-hydroxy-3,4-dihydroisocoumarin
CS-0225132
NS00094872
E82508
EN300-1228708
Q6813065
3-Methyl-8-hydroxy-3,4-dihydro-1H-2-benzopyran-1-one
Z1198723372
Isocoumarin, 3,4-dihydro-8-hydroxy-3-methyl, (.+/-.)-
3,4-Dihydro-8-hydroxy-3-methyl-1H-2-benzopyran-1-one, (.+/-.)-
InChI=1/C10H10O3/c1-6-5-7-3-2-4-8(11)9(7)10(12)13-6/h2-4,6,11H,5H2,1H
Solubility of 8-hydroxy-3-methyl-isochroman-1-one
8-hydroxy-3-methyl-isochroman-1-one, with its unique structure, exhibits specific solubility characteristics that are of interest in various applications. Its solubility can often depend on several factors, including:
As a noteworthy point, it is essential to consider solvent interactions that can increase solubility. For instance, solvents capable of hydrogen bonding can significantly enhance the dissolution of 8-hydroxy-3-methyl-isochroman-1-one. This characteristic makes it a viable candidate for applications in pharmaceuticals and organic synthesis, where solubility plays a critical role in reactivity and availability.
In conclusion, understanding the solubility behavior of 8-hydroxy-3-methyl-isochroman-1-one is crucial for optimizing its use in various chemical processes, highlighting the importance of choosing the right solvent and conditions for increased efficacy.