33539-20-7

Basic information

• Product Name: Ethanone, 1-(3,6-dihydroxy-2-methoxyphenyl)-
• Synonyms: 2,7-DIHYDROXY NAPHTHALENE-3,6-DISULPHONATE;3,6-dihydroxy-2-methoxyacetophenone;3,6-Dihydroxynaphthalene-2,7-Disulfonic Acid;6-methoxy-2,5-dihydroxyacetophenone;2,5-dihydroxy-6-methoxyacetophenone;3,6-Dihydroxy-naphthalin-2,7-disulfonsaeure;2,7-Naphthalenedisulfonic acid,3,6-dihydroxy;3,6-dihydroxy-2,7-naphthalenesulfonic acid;2-acetyl-3-methoxy-hydroquinone;2,4-dihydroxy-6-methoxy acetophenone;2,7-Dihydroxy-3,6-naphthalenedisulfonic acid
• CAS NO: 33539-20-7
• Molecular Formula: C9H10O4
• Molecular Weight: 182.176
• Mol File: 33539-20-7.mol
• Article Data: 8

Chemical Properties

• Melting Point: 91°C
• CAS DataBase Reference: Ethanone, 1-(3,6-dihydroxy-2-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3,6-dihydroxy-2-methoxyphenyl)-(33539-20-7)
• EPA Substance Registry System: Ethanone, 1-(3,6-dihydroxy-2-methoxyphenyl)-(33539-20-7)

Safety Data

• Hazardous Substances Data: 33539-20-7(Hazardous Substances Data)

Usage

Preparation

Preparation from 2-hydroxy-6-methoxyacetophenone by persulfate oxidation (Elbs reaction) (26–33%).

Upstream product

• 67-56-1 methanol 
• 490-78-8 2,5-Dihydroxyacetophenone 
• 699-83-2 2,6-dihydroxylacetophenone 
• 703-23-1 2'-hydroxy-6'-methoxyacetophenone 
• 2555-29-5 8-acetyl-7-hydroxy-4-methyl-2H-chromen-2-one 
• 1125-55-9 2-Acetyl-1,4-benzoquinone 

Downstream Products

• 6665-66-3 5,6-Dihydroxyflavone 
• 118021-60-6 6-hydroxy-5-methoxy-2-phenyl-4H-chromen-4-one 
• 85395-95-5 5-hydroxy-6-methoxy-2-phenyl-4H-chromen-4-one 
• 33554-48-2 5,6-dimethoxyflavone 
• 6665-77-6 5,6-diacetoxy-2-phenyl-chromen-4-one 
• 1187652-32-9 2-[(4-chloro-benzylamino)-methyl]-5,6-dihydroxy-chromen-4-one 
• 1187652-33-0 2-[(3-chloro-benzylamino)-methyl]-5,6-dihydroxy-chromen-4-one 
• 1187652-42-1 acetic acid 2-acetyl-4-benzyloxy-3-methoxy-phenyl ester 
• 1312762-15-4 C₂₅H₂₂ClNO₄ 
• 1312762-08-5 C₂₅H₂₂ClNO₄ 
• 1187652-43-2 6-benzyloxy-5-methoxy-2-methyl-chromen-4-one 
• 1187652-44-3 6-benzyloxy-5-methoxy-4-oxo-4H-chromene-2-carbaldehyde 
• 1312761-87-7 C₁₇H₁₄BrNO₄ 
• 1312761-88-8 C₁₇H₁₄INO₄ 

Relevant articles and documents

2-Arylmethylaminomethyl-5,6-dihydroxychromone derivatives with selective anti-HCV activity

Anti-HCV activity of aryl diketoacid (ADK) has been characterized by its two pharmacophoric elements, α,β-diketo acid moiety and substituted aryl ring. In this study, as a part of our ongoing efforts to discover a novel anti-HCV compound mimicking the ADK

FLAVONES

The present invention relates to flavone compounds and their use in methods of treating or preventing parasitic infections, fungal infections and cell proliferative disorders. The present invention also relates to the use of flavone compounds in methods of controlling pests.

A New and Facile Iodine(III)-Mediated Approach for the Regioselective Alkoxylation of 2,5-Dihydroxyacetophenone

Oxidation of 2,5-dihydroxyacetophenone with iodobenzene diacetate (IBD) in different alcohols leads to regioselective alkoxylation, thereby providing a new and convenient route for the synthesis of 6-alkoxy-2,5- dihydroxyacetophenones.