142942-21-0

Basic information

• Product Name: 1,10-Phenanthroline, 2-(4-methoxyphenyl)-
• CAS NO: 142942-21-0
• Molecular Formula: C19H14N2O
• Molecular Weight: 286.333
• Mol File: 142942-21-0.mol

Chemical Properties

• CAS DataBase Reference: 1,10-Phenanthroline, 2-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-Phenanthroline, 2-(4-methoxyphenyl)-(142942-21-0)
• EPA Substance Registry System: 1,10-Phenanthroline, 2-(4-methoxyphenyl)-(142942-21-0)

Safety Data

• Hazardous Substances Data: 142942-21-0(Hazardous Substances Data)

Usage

Uses

Used in Coordination Chemistry:
1,10-Phenanthroline, 2-(4-methoxyphenyl)is used as a ligand in coordination chemistry for forming complexes with metal ions. The application reason is its ability to chelate with metal ions, enhancing the stability and reactivity of the resulting complexes.
Used in Biological Studies:
1,10-Phenanthroline, 2-(4-methoxyphenyl)is used as a research tool in biological studies for investigating the interactions between metal ions and biomolecules. The application reason is its potential to modulate the activity of metalloenzymes and other metal-binding proteins.
Used in Organic Synthesis:
1,10-Phenanthroline, 2-(4-methoxyphenyl)is used as a building block in the synthesis of other organic compounds. The application reason is its unique structural features, which can be exploited to create novel molecules with specific properties and functions.

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 66-71-7 1,10-Phenanthroline 
• 14774-77-7 p-methoxyphenyllithium 

Downstream Products

• 142942-22-1 2-methyl-9-(p-anisyl)-1,10-phenanthroline 
• 142942-24-3 C₄₄H₃₈N₄O₂ 
• 159726-85-9 (C₁₂H₆N₂C₆H₄OCH₃)2C₆H₄ 
• 201403-32-9 2-(p-methoxyphenyl)-9-(5'-methylpyridin-2'-yl)-1,10-phenanthroline 
• 188637-85-6 (tris(2-pyridylmethyl)amine)copper(I) hexafluorophosphate 
• 782491-09-2 (Cu(N₂C₁₂H₆(C₆H₄OCH₂CH₂OCH₂CH₂OCH₂)2)(N₂C₁₈H₁₁OCH₃))⁽¹⁺⁾*PF₆^(1-)=(Cu(N₂C₁₂H₆(C₆H₄OCH₂CH₂OCH₂CH₂OCH₂)2)(N₂C₁₈H₁₁OCH₃))PF₆ 
• 889663-74-5 bis(2-p-anisyl-1,10-phenanthroline)copper(I) hexafluorophosphate 
• 142942-23-2 C₄₀H₃₀N₄O₂ 
• 159726-86-0 m-bis(2-(p-hydroxyphenyl)-1,10-phenanthrolinyl)benzene 
• 1260105-36-9 (C₁₅N₃H₁₀C₆H₄CH₃)Ru(CH₃OC₆H₃C₁₂N₂H₇)⁽¹⁺⁾*PF₆^(1-)=C₁₅N₃H₁₀C₆H₄CH₃RuCH₃OC₆H₃C₁₂N₂H₇PF₆ 

Relevant articles and documents

A trefoil knotted polymer produced through ring expansion

A synthetic strategy is reported for the production of a trefoil knotted polymer from a copper(I)-templated helical knot precursor through ring expansion. The expected changes in the properties of the knotted polymer compared to a linear analogue, for exa

New rhenium(i) complexes with substituted diimine ligands for highly efficient phosphorescent devices fabricated by a solution process

A series of new carbonyl rhenium(i) complexes chelated by a substituted 1,10-phenanthroline ligand with the general formula Re(CO)3LCl, where L = 2-(2′-methoxyphenyl)-1,10-phenanthroline (L1), 2-(4′-methoxyphenyl)-1,10-phenanthroline

Dicopper(I) trefoil knots and related unknotted molecular systems: Influence of ring size and structural factors on their synthesis and electrochemical and excited-state properties

Five new dicopper(I) knots have been synthesized as well as their face-to-face isomers. The knots range from 80- to 90-membered rings, and their preparation yields depend crucially on structural parameters such as number of methylene fragments linking the