167276-19-9

Usage

Chemical structure

A complex compound containing multiple hydroxyl groups and a benzopyran ring structure.

Hexahydroand trioxanaphthacene-12-one derivative

Indicates the presence of six hydrogen atoms and three oxygen atoms in the naphthacene ring structure.

Potential applications

Has potential implications in pharmaceutical, biotechnological, and medical research due to its unique and complex structure.

Further research needed

More studies and research are required to fully understand its properties and potential applications.

Molecular weight

Approximately 610.52 g/mol

Appearance

Likely a solid, due to the presence of multiple hydroxyl groups and the complex structure.

Solubility

Likely soluble in polar solvents such as water or methanol, due to the presence of hydroxyl groups.

Stability

May be sensitive to heat, light, or air, due to the presence of multiple hydroxyl groups and the complex structure.

Reactivity

May react with other chemicals, such as acids or bases, due to the presence of hydroxyl groups.

Upstream product

• 117-39-5 quercetol 

Downstream Products

• 1383562-38-6 C₁₅₈H₂₅₈O₂₂ 
• 1383562-29-5 1,3-bis-butyryloxy-11a-hydroxy-9-(3,5,7-tributyryloxy-4H-1-benzopyran-4-on-2-yl)-5a-(3,4-bisbutyryloxyphenyl)-5,5a,6,11,11a,12-hexahydro-5,6,11-trioxanaphthacene-12-one 

Relevant academic research and scientific papers

Structure of doubly-linked oxidative product of quercetin in lipid peroxidation

From quercetin during autoxidation of unsaturated lipid and radical reaction, a novel doubly-linked oxidative product was isolated and its structure has been characterized to be 1,3,11a-trihydroxy-9-(3,5,7-trihydroxy-4H-1-benzopyran-4-on-2-yl)-5a-(3,4-dih

A new flavonol glucoside from onion

A new flavonol glucoside was isolated from the outer bulb of onions (Allium cepa). The structure was determined by the analysis of spectral data.

Novel quercetin derivatives: Synthesis and screening for anti-oxidant activity and aldose reductase inhibition

The direct acylation of quercetin (I) with 3-chloro-2,2-dimethylpropanoyl chloride (II) gives a complex reaction mixture. The synthesis of different acylated quercetin with from mono- to tetra-O-substituted functions was achieved in a simple procedure whe

Novel quercetin derivatives, their preparation, pharmaceutical compositions containing them and their use

The invention relates to novel quercetin derivatives and pharmaceutically acceptable salts, hydrates, and solvates and dimers thereof; a process for the preparation of the novel quercetin derivatives and pharmaceutically acceptable salts, hydrates, and so

Oligomeric oxidation products of the flavonoid quercetin

Some of the main oxidation products of quercetin were shown to be compounds formed by oligomerization of the starting flavonoid. Conditions for the preparative synthesis of these compounds were developed. Their structures were established using HPLC-MS an