7089-67-0

Basic information

• Product Name: 1,10-phenanthrolin-4-broMo-
• Synonyms: 1,10-phenanthrolin-4-broMo-;1,10-Phenanthroline, 4-broMo-;4-broMo-1,10-phenanthroline
• CAS NO: 7089-67-0
• Molecular Formula: C₁₂H₇BrN₂
• Molecular Weight: 259.10138
• Mol File: 7089-67-0.mol

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 1,10-phenanthrolin-4-broMo-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-phenanthrolin-4-broMo-(7089-67-0)
• EPA Substance Registry System: 1,10-phenanthrolin-4-broMo-(7089-67-0)

Safety Data

• Hazardous Substances Data: 7089-67-0(Hazardous Substances Data)

Usage

Uses

Used in Catalysis:
1,10-Phenanthrolin-4-bromois used as a catalyst in various chemical reactions for its unique properties that can enhance the reaction efficiency and selectivity.
Used in Organic Synthesis:
1,10-Phenanthrolin-4-bromois used as a reagent or intermediate in organic synthesis for the preparation of various organic compounds, taking advantage of its reactivity and properties.
Used in Material Science:
1,10-Phenanthrolin-4-bromois used in the development of new materials with specific properties, such as conductivity, magnetism, or optical properties, by exploiting its coordination chemistry capabilities.
Overall, 1,10-phenanthrolin-4-bromois a valuable chemical compound with diverse potential applications in research and industrial settings, including catalysis, organic synthesis, and material science.

Upstream product

• 93533-15-4 1H-1,10-phenanthrolin-4-one 
• 23443-31-4 4-hydroxy-1,10-phenanthroline 
• 95-54-5 1,2-diamino-benzene 
• 503863-91-0 1,2-bis-[(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidenemethyl)amino]benzene 
• 87330-27-6 1,4,7,10-tetrahydro-1,10-phenanthroline-4,7-dione 
• 156492-30-7 4,7-dibromo-1,10-phenanthroline 

Downstream Products

• 97802-07-8 4-p-bromophenyl-1,10-phenanthroline 

Relevant articles and documents

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

Synthesis of aryl-substituted 2-pyridyl-1,10-phenanthrolines; A series of oriented terpyridine analogues

A 3 × 3 matrix of manisyl (4-methoxy-2,6-dimethylphenyl) substituted pyridyl-1,10-phenanthrolines has been synthesized by utilizing a general palladium catalyzed cross-coupling procedure. The directionality of these terdentate ligands will generate chiral

A total synthesis of subarine, a marine alkaloid related to the pyridoacridine family

The synthesis of the marine alkaloid subarine has been accomplished in four steps in 70% overall yield starting from 4-bromo-1,10-phenanthroline. The natural compound and three intermediates in the synthesis were tested at six concentrations on six differ