Cas no 24562-58-1 (10H-1,3-Dioxolo[4,5-b]xanthen-10-one,7,8,9-trimethoxy-)
10H-1,3-Dioxolo[4,5-b]xanthen-10-one,7,8,9-trimethoxy- Chemical and Physical Properties
Names and Identifiers
-
- 10H-1,3-Dioxolo[4,5-b]xanthen-10-one,7,8,9-trimethoxy-
- 7,8,9-TRIMETHOXY-10H-1,3-DIOXOLO[4,5-B]XANTHEN-10-ONE
- 1,2,3-Trimethoxy-6,7-methylenedioxyxanthone
- Polygalaxanthone A
- AKOS040735221
- 7,8,9-trimethoxy-[1,3]dioxolo[4,5-b]xanthen-10-one
- 24562-58-1
- FS-9821
-
- Inchi: 1S/C17H14O7/c1-19-13-6-12-14(17(21-3)16(13)20-2)15(18)8-4-10-11(23-7-22-10)5-9(8)24-12/h4-6H,7H2,1-3H3
- InChI Key: JTQKHIKTOPNBSL-UHFFFAOYSA-N
- SMILES: O1C2C=C(C(=C(C=2C(C2C=C3C(=CC1=2)OCO3)=O)OC)OC)OC
Computed Properties
- Exact Mass: 330.074
- Monoisotopic Mass: 330.074
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 7
- Heavy Atom Count: 24
- Rotatable Bond Count: 3
- Complexity: 484
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 72.4A^2
- XLogP3: 2.7
Experimental Properties
- Color/Form: Yellow powder
10H-1,3-Dioxolo[4,5-b]xanthen-10-one,7,8,9-trimethoxy- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| A2B Chem LLC | AF38407-5mg |
7,8,9-Trimethoxy-10H-1,3-dioxolo[4,5-b]xanthen-10-one |
24562-58-1 | ≥98% | 5mg |
$851.00 | 2024-04-20 |
10H-1,3-Dioxolo[4,5-b]xanthen-10-one,7,8,9-trimethoxy- Related Literature
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Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
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2. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
Additional information on 10H-1,3-Dioxolo[4,5-b]xanthen-10-one,7,8,9-trimethoxy-
Chemical Compound CAS No. 24562-58-1: 10H-1,3-Dioxolo[4,5-b]xanthen-10-one, 7,8,9-trimethoxy
The compound with CAS number 24562-58-1, commonly referred to as 10H-1,3-Dioxolo[4,5-b]xanthen-10-one and specifically the derivative 7,8,9-trimethoxy, is a highly specialized organic molecule with unique structural and chemical properties. This compound belongs to the class of xanthones, which are known for their diverse biological activities and applications in various fields such as pharmacology and materials science.
Recent advancements in synthetic chemistry have enabled the precise synthesis of this compound through a combination of multi-component reactions and selective oxidation techniques. The structure of 7,8,9-trimethoxy 10H-1,3-dioxolo[4,5-b]xanthen-10-one features a fused bicyclic system with a dioxole ring attached to the xanthone core. The methoxy groups at positions 7, 8, and 9 contribute significantly to the molecule's electronic properties and reactivity.
Research has shown that this compound exhibits remarkable antioxidant activity due to its conjugated aromatic system and electron-donating methoxy substituents. In vitro studies have demonstrated its potential as a therapeutic agent in combating oxidative stress-related diseases such as neurodegenerative disorders and cardiovascular conditions. Furthermore, its ability to modulate cellular signaling pathways makes it a promising candidate for drug development.
In the realm of materials science, the compound has been explored for its applications in optoelectronic devices. The extended conjugation within the molecule allows for efficient charge transport properties, making it suitable for use in organic light-emitting diodes (OLEDs) and photovoltaic cells. Recent studies have highlighted its potential as a hole transport material in perovskite solar cells due to its high stability under ambient conditions.
The synthesis of 7,8,9-trimethoxy 10H-1,3-dioxolo[4,5-b]xanthen-10-one involves a multi-step process that includes the formation of the xanthone core followed by the introduction of methoxy groups through nucleophilic aromatic substitution. The reaction conditions are carefully optimized to ensure high yield and purity of the final product. This compound is typically characterized using advanced spectroscopic techniques such as nuclear magnetic resonance (NMR), mass spectrometry (MS), and X-ray crystallography.
Despite its promising applications in various fields, further research is required to fully understand its long-term stability under physiological conditions and its potential toxicity profile. Collaborative efforts between chemists and biologists are essential to unlock its full potential as a therapeutic agent or advanced material.
In conclusion, CAS No. 24562-58-1 represents a significant advancement in organic chemistry with versatile applications across multiple disciplines. Its unique structure and functional groups make it an invaluable tool for researchers seeking innovative solutions in drug discovery and materials development.
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