517-48-6

Basic information

• Product Name: 2,2',4,4',5,5'-Hexahydroxy-7,7'-dimethyl-1,1'-bi[anthracen-10(9H)-one]
• Synonyms: 2,2',4,4',5,5'-Hexahydroxy-7,7'-dimethyl-1,1'-bi[anthracen-10(9H)-one];Penicilliopsin
• CAS NO: 517-48-6
• Molecular Formula: C₃₀H₂₂O₈
• Molecular Weight: 510.49
• Mol File: 517-48-6.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2',4,4',5,5'-Hexahydroxy-7,7'-dimethyl-1,1'-bi[anthracen-10(9H)-one](CAS DataBase Reference)
• NIST Chemistry Reference: 2,2',4,4',5,5'-Hexahydroxy-7,7'-dimethyl-1,1'-bi[anthracen-10(9H)-one](517-48-6)
• EPA Substance Registry System: 2,2',4,4',5,5'-Hexahydroxy-7,7'-dimethyl-1,1'-bi[anthracen-10(9H)-one](517-48-6)

Safety Data

• Hazardous Substances Data: 517-48-6(Hazardous Substances Data)

Usage

Chemical Class

Polyaromatic ketone

Explanation

The compound has a complex structure based on multiple interconnected aromatic rings and a ketone group.

Explanation

The presence of six hydroxyl groups contributes to its solubility, reactivity, and interaction with other molecules.

Explanation

The two methyl groups are attached to the anthracene backbone, influencing the compound's stability and physical properties.
4. Derived from Anthraquinone Family

Explanation

The compound originates from the anthraquinone family, which is known for its chemical and structural diversity.
5. Intense Color and Fluorescence Properties

Explanation

The complex structure and presence of multiple hydroxyl and methyl groups give the compound its unique color and fluorescence, making it suitable for use as a dye.
6. Use in Optical Brightening Agents

Explanation

The compound's fluorescence properties make it an ideal choice for use in optical brightening agents to enhance the appearance of materials.
7. Potential Medical Applications

Explanation

The compound's unique structure and properties may lead to potential applications in the field of medicine, such as drug development or imaging agents.
8. Polymerization Catalyst

Explanation

The compound can act as a catalyst in polymerization reactions, facilitating the formation of polymers with specific properties.
9. Organic Electronic Devices

Explanation

The compound's electronic properties make it a potential candidate for use in organic electronic devices, such as organic light-emitting diodes (OLEDs) or organic solar cells.

Hydroxyl Groups

Six (OH) groups

Methyl Groups

Two (CH3) groups

Downstream Products

• 613-12-7 2-methylanthracene 
• 602-14-2 3-hydroxy-5-methyl-2,4,6-trinitro-benzoic acid 
• 797043-43-7 1,3,8-trihydroxy-6-methyl-2,4,5,7-tetranitro-anthraquinone 
• 144-62-7 oxalic acid 
• 491-60-1 emodinanthrone