87330-27-6

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 
• 97802-07-8 4-p-bromophenyl-1,10-phenanthroline 
• 7089-67-0 4-bromo-1,10-phenanthroline 

Relevant academic research and scientific papers

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

Organic electroluminescence material and organic photoelectric device

The invention provides a compound with a structure as shown in formula I. The invention also provides an application of the compound in an organic photoelectric device and the organic photoelectric device. The compound provided by the invention has a ther

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.

The Synthesis of Pyridoquinolines with Dialkylaminopropylamine Side Chains

Several new pyridoquinolines with dimethylaminopropyl side chains including 4,7-bis(3'-dimethylaminopropylamino)-1,10-phenanthroline (1), 4,10-bis(3'-dimethylaminopropylamino)-1,7-phenanthroline (2), 4,10-bis(3'-dimethylaminopropylamino)-6-methyl-1,7-phen