71335-86-9

Basic information

• Product Name: 1-hydroxy-4-{[4-(2-hydroxyethyl)phenyl]amino}anthracene-9,10-dione
• CAS NO: 71335-86-9
• Molecular Formula: C₂₂H₁₇NO₄
• Molecular Weight: 359.3747
• Mol File: 71335-86-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 570.8°C at 760 mmHg
• Flash Point: 299°C
• Density: 1.415g/cm³
• Vapor Pressure: 7.22E-14mmHg at 25°C
• Refractive Index: 1.726
• CAS DataBase Reference: 1-hydroxy-4-{[4-(2-hydroxyethyl)phenyl]amino}anthracene-9,10-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-hydroxy-4-{[4-(2-hydroxyethyl)phenyl]amino}anthracene-9,10-dione(71335-86-9)
• EPA Substance Registry System: 1-hydroxy-4-{[4-(2-hydroxyethyl)phenyl]amino}anthracene-9,10-dione(71335-86-9)

Safety Data

• Hazardous Substances Data: 71335-86-9(Hazardous Substances Data)

Usage

Derivative of anthracene

Originates from anthracene, a tricyclic aromatic hydrocarbon, indicating a similar core structure.

Hydroxyethyl group

Contains a functional group with an alcohol (-OH) group attached to an ethyl (-CH2-CH3) group, which may contribute to its potential antioxidant and cytoprotective properties.

Amino group

Features an amino group (-NH2) attached to the central benzene ring, which may play a role in its biological activities and potential applications in medical research.

Potential antioxidant properties

HPEA has been studied for its ability to neutralize free radicals and protect cells from oxidative damage, which could be beneficial in the treatment of various diseases.

Cytoprotective properties

The compound has shown promise in protecting cells from damage or death, which may be useful in treating certain types of cancer.

Cancer treatment potential

HPEA has been investigated for its use in targeting and destroying cancer cells, particularly in combination with other therapeutic agents.

Photodynamic therapy

The compound has been explored for its potential use in photodynamic therapy, a treatment that utilizes light-sensitive compounds to selectively target and eliminate cancer cells.

Ongoing research

Further studies are needed to fully understand the potential uses and effects of 1-hydroxy-4-[4-(2-hydroxyethyl)phenyl]aminoanthracene-9,10-dione, as its unique structure and biological activities make it an intriguing subject for scientific inquiry.

Upstream product

• 81-64-1 1,4-dihydroxy-9,10-anthracenedione 
• 17648-03-2 9,10-Dihydroxy-2,3-dihydro-anthracene-1,4-dione 
• 104-10-9 2-(4'-aminophenyl)ethyl alcohol 

Downstream Products

• 1310893-71-0 1-(4-(2-(allylaminocarbonyloxy)ethyl)phenyl)amino-4-hydroxyanthraquinone 
• 1310893-73-2 1-(4-(2-methacryloyloxyethyl)phenyl)amino-4-hydroxy-9,10-anthraquinone 

Relevant articles and documents

Colorant compounds

Compounds of the formula wherein M is either (1) a metal ion having a positive charge of +y wherein y is an integer which is at least 2, said metal ion being capable of forming a compound with at least two chromogen moieties, or (2) a metal-containing moiety capable of forming a compound with at least two chromogen moieties, z is an integer representing the number of chromogen moieties associated with the metal and is at least 2, R1, R2, R3, R4, R5, R6, R7, a, b, c, d, Y, and z are as defined herein, Q? is a COO? group or a SO3— group, A is an organic anion, and CA is either a hydrogen atom or a cation associated with all but one of the Q? groups.

Methods for making colorant compounds

Disclosed is a process for preparing a colorant of the formula 1wherein Y is a hydrogen atom or a bromine atom, n is an integer of 0, 1, 2, 3, or 4, R1 is an alkylene group or an arylalkylene group, R2 is an alkyl group, an aryl grou