87330-27-6

Basic information

• Product Name: 1,4,7,10-tetrahydro-1,10-phenanthroline-4,7-dione
• CAS NO: 87330-27-6
• Molecular Weight: 212.208
• Mol File: 87330-27-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: >300 °C (decomp)
• Boiling Point: 417.9±45.0 °C(Predicted)
• Density: 1.371±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,4,7,10-tetrahydro-1,10-phenanthroline-4,7-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4,7,10-tetrahydro-1,10-phenanthroline-4,7-dione(87330-27-6)
• EPA Substance Registry System: 1,4,7,10-tetrahydro-1,10-phenanthroline-4,7-dione(87330-27-6)

Safety Data

• Hazardous Substances Data: 87330-27-6(Hazardous Substances Data)

Usage

Type of compound

Heterocyclic compound

Structure

Contains a phenanthroline skeleton and a dione functional group

Color

Yellow-orange

Solubility

Sparingly soluble in water

Applications

a. Synthesis of pharmaceuticals
b. Ligand in coordination chemistry (chelates with metal ions to form stable complexes)
c. Production of dyes
d. Catalysts
e. Materials for organic electronics

Investigated properties

a. Antimicrobial activity
b. Antifungal properties

Upstream product

• 87330-26-5 1,4,7,10-tetrahydro-3,8-dicarboxy-1,10-phenanthroline-4,7-dione 
• 95-54-5 1,2-diamino-benzene 
• 87330-25-4 1,4,7,10-tetrahydro-3,8-bis(ethoxycarbonyl)-1,10-phenanthroline-4,7-dione 
• 4921-71-5 N,N'-bis(2,2-di{ethoxycarbonyl}ethenyl)-1,2-diamino-benzene 
• 503863-91-0 1,2-bis-[(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidenemethyl)amino]benzene 

Downstream Products

• 5394-23-0 4,7-dichloro-1,10-phenanthroline 
• 156492-30-7 4,7-dibromo-1,10-phenanthroline 
• 7089-67-0 4-bromo-1,10-phenanthroline 
• 97802-07-8 4-p-bromophenyl-1,10-phenanthroline 

Relevant articles and documents

A novel photosensitizer based on a ruthenium(ii) phenanthroline bis(perylenediimide) dyad: synthesis, generation of singlet oxygen and in vitro photodynamic therapy

In this study, a novel photosensitizer having two perylenediimide units and a phenanthroline ruthenium(ii) coordination moiety (Ru-BP) has been developed for photodynamic therapy (PDT) of cancer cells. This new compound was prepared via reactions of two n

The synthesis of aromatic diazatricycles from phenylenediamine-bis(methylene Meldrum's acid) derivatives

The thermocyclisation of phenylenediamine-bis(methylene Meldrum's acid) derivatives has been investigated. Those of o-phenylenediamines give 1,10-phenanthroline derivatives, while those of m- and p-phenylenediamines lead to the preferential formation of angular diazatricycles. Thus, for example, the di-Meldrum's acid derivative of 2,5-dichloro-1,4-phenylenediamine gives, via ipso-substitution, the unexpected angular product 19.