69657-89-2

Basic information

• Product Name: 1,4-dihydroxy-5,8-bis[(2-phenylethyl)amino]anthracene-9,10-dione
• Synonyms: 1,4-Dihydroxy-5,8-bis[(2-phenylethyl)amino]-9,10-anthraquinone; 9,10-anthracenedione, 1,4-dihydroxy-5,8-bis[(2-phenylethyl)amino]-
• CAS NO: 69657-89-2
• Molecular Formula: C₃₀H₂₆N₂O₄
• Molecular Weight: 478.5384
• Mol File: 69657-89-2.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 780.2°C at 760 mmHg
• Flash Point: 425.7°C
• Density: 1.37g/cm³
• Vapor Pressure: 3.01E-25mmHg at 25°C
• Refractive Index: 1.733
• CAS DataBase Reference: 1,4-dihydroxy-5,8-bis[(2-phenylethyl)amino]anthracene-9,10-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-dihydroxy-5,8-bis[(2-phenylethyl)amino]anthracene-9,10-dione(69657-89-2)
• EPA Substance Registry System: 1,4-dihydroxy-5,8-bis[(2-phenylethyl)amino]anthracene-9,10-dione(69657-89-2)

Safety Data

• Hazardous Substances Data: 69657-89-2(Hazardous Substances Data)

Usage

Chemical structure

A synthetic compound derived from anthracene-9,10-dione with two hydroxyl groups and two amino groups connected to the anthracene structure by phenylethyl groups.

Molecular weight

Approximately 540.6 g/mol

Appearance

Yellow to orange crystalline solid

Solubility

Soluble in organic solvents such as dimethyl sulfoxide (DMSO) and methanol, but not very soluble in water.

Medical research

Studied for its potential use in cancer treatment due to its ability to inhibit the growth of certain cancer cells.

Antioxidant properties

Investigated for its antioxidant properties, which may have potential applications in various medical and industrial fields.

Photodynamic therapy

Explored for its potential use in photodynamic therapy, a treatment that involves the use of light-sensitive compounds to target and destroy cancer cells.

Complex structure

The unique arrangement of hydroxyl, amino, and phenylethyl groups in the molecule contributes to its interesting and valuable properties in the fields of medicine and chemistry.

Synthesis

The compound is synthesized through a series of chemical reactions, typically involving the formation of the anthracene-9,10-dione core and subsequent functionalization with the phenylethyl groups and hydroxyl/amino substitutions.

Stability

Relatively stable under normal laboratory conditions, but may be sensitive to light, heat, and moisture.

Safety precautions

As with any synthetic compound, appropriate safety measures should be taken when handling 1,4-dihydroxy-5,8-bis[(2-phenylethyl)amino]anthracene-9,10-dione, including the use of gloves, eye protection, and a fume hood.

Purity

The purity of the compound can be determined using techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry.

Structural analysis

The structure of the compound can be confirmed using techniques like nuclear magnetic resonance (NMR) spectroscopy and X-ray crystallography.

Biological activity

Further research is needed to fully understand the biological activity and potential therapeutic applications of 1,4-dihydroxy-5,8-bis[(2-phenylethyl)amino]anthracene-9,10-dione.