22225-63-4

Basic information

• Product Name: 1-hydroxy-3-methoxy-6-methylanthracene-9,10-dione
• Synonyms: 1-Hydroxy-3-methoxy-6-methylanthra-9,10-quinone; 1-Hydroxy-3-methoxy-6-methylanthraquinone
• CAS NO: 22225-63-4
• Molecular Formula: C₁₆H₁₂O₄
• Molecular Weight: 268.2641
• Mol File: 22225-63-4.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 502.2°C at 760 mmHg
• Flash Point: 193°C
• Density: 1.356g/cm³
• Vapor Pressure: 1.05E-10mmHg at 25°C
• Refractive Index: 1.649
• CAS DataBase Reference: 1-hydroxy-3-methoxy-6-methylanthracene-9,10-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-hydroxy-3-methoxy-6-methylanthracene-9,10-dione(22225-63-4)
• EPA Substance Registry System: 1-hydroxy-3-methoxy-6-methylanthracene-9,10-dione(22225-63-4)

Safety Data

• Hazardous Substances Data: 22225-63-4(Hazardous Substances Data)

Upstream product

• 52062-24-5 (E)-1-acetoxy-3-methyl-1,3-butadiene 
• 65120-69-6 3-chloro-5-hydroxy-7-methoxy-1,4-naphthoquinone 
• 83823-73-8 1,3-dimethoxy-6-methylanthracene-9,10-dione 
• 116888-98-3 (1RS,2SR,3RS,4aRS,9aRS)-2,3-epoxy-1,2,3,4,4a,9a-hexahydro-8-hydroxy-2-methyl-1-(trimethylsiloxy)-9,10-anthraquinone 
• 116888-94-9 (1RS,4aRS,9aRS)-5-acetoxy-1,4,4a,9a-tetrahydro-7-methoxy-1-(trimethylsiloxy)-9,10-anthraquinone 
• 116888-97-2 (1RS,2RS,3RS,4aRS,9aRS)-5-acetoxy-2,3-epoxy-1,2,3,4,4a,9a-hexahydro-7-methoxy-2-methyl-1-(trimethylsiloxy)-9,10-anthraquinone 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 481-39-0 5-hydroxynaphtho-1,4-quinone 
• 70063-61-5 5-hydroxy-7-methoxy-1,4-naphthoquinone 
• 116888-93-8 5-acetoxy-7-methoxy-1,4-naphthoquinone 
• 116888-95-0 (1RS,4aRS,9aRS)-1,4,4a,9a-tetrahydro-8-hydroxy-2-methyl-1-(trimethylsiloxy)-9,10-anthraquinone 
• 83823-70-5 2,4-Dimethoxy-6-(3-methyl-benzyl)-benzoic acid 
• 83823-66-9 2,4-Dimethoxy-6-(3-methyl-benzyl)-benzoic acid ethyl ester 
• 137822-31-2 (+/-)-1-deoxyaustrocortirubin 

Relevant articles and documents

New antitumour fungal metabolites from Alternaria porri

Chemical investigation of the onion pathogenic fungus Alternaria porri resulted in the isolation of two new phthalides named zinnimide (2) and deprenylzinnimide (8), along with a new bianthraquinone, alterporriol F (10). The structures of the new metabolites were characterised by spectroscopic analysis and chemical degradation. Of the new compounds isolated, alterporriol F was highly cytotoxic towards HeLa and KB cells, with IC50 values of 6.5 and 7.0 g mL-1.

An investigation of the reaction mechanism of the bis-acylation of aromatics with o-phthaloyl dichlorides: Regioselective synthesis of anthraquinones

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Pigments of fungi. LXV Tetrahydroanthraquinone and anthraquinone gentiobiosides from the fungus Dermocybe splendida

The tetrahydroanthraquinones (1S,3S)-austrocortirubin (7) and (1S,3S)-austrocortilutein (10) and the anthraquinones austrocortinin (13), xanthorin (14) and 3-methylxanthopurpurin 6-O-methyl ether (15) occur in the fungus Dermocybe splendida mainly in the form of their respective 8-O-β-D-gentiobiosides (26), (11), (16), (19) and (22) (gentiobiose = 6-O-β-D-glucopyranosyl-β-D-glucopyranose). The various gentiobiosides are isolated from lyophilized fruit bodies, separated by chromatography and characterized, in the main, as their acetyl derivatives by spectroscopic and chemical methods. A method for the selective cleavage of phenolic acetyl groups in peracetylated anthraquinone and tetrahydroanthraquinone glycosides is described. CSIRO 2000.