21722-08-7

Basic information

• Product Name: 1-Phenyl-1H-iMidazol-2-aMine
• Synonyms: 1-Phenyl-1H-iMidazol-2-aMine
• CAS NO: 21722-08-7
• Molecular Formula: C₉H₉N₃
• Molecular Weight: 159.18786
• Mol File: 21722-08-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 1-Phenyl-1H-iMidazol-2-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Phenyl-1H-iMidazol-2-aMine(21722-08-7)
• EPA Substance Registry System: 1-Phenyl-1H-iMidazol-2-aMine(21722-08-7)

Safety Data

• Hazardous Substances Data: 21722-08-7(Hazardous Substances Data)

Usage

General Description

1-Phenyl-1H-imidazol-2-amine is a chemical compound that belongs to the class of imidazole derivatives. It is a white solid with a molecular formula C9H9N3 and a molecular weight of 159.19 g/mol. 1-Phenyl-1H-iMidazol-2-aMine is commonly used as a building block for the synthesis of other pharmaceuticals and organic compounds. It is also known for its ability to act as a ligand in coordination chemistry, forming complexes with various metal ions. Additionally, 1-Phenyl-1H-imidazol-2-amine has potential biological activities and is being researched for its pharmacological properties, including as an antidote for nerve agents and as a potential treatment for certain neurological disorders.

Upstream product

• 7720-39-0 1H-imidazol-2-amine 
• 591-50-4 iodobenzene 

Relevant articles and documents

Rational design of nickel catalysts containing N-acylated imidazolin-2-imine ligand for ethylene copolymerization with polar monomer

By taking advantage of electronic influence of ligand design, the novel neutral nickel complexes bearing strong electron-donating N-acylated imidazolin-2-imine ligand were synthesized and characterized. The nickel catalysts conducted ethylene polymerization with high activity and good thermal stability, affording semicrystalline polyethylene with short chain branches (32–46/1000 C atoms). The complex Ni2 bearing adamantyl substituent on the imidazoline ligand showed higher activity than phenyl substituted complex Ni1, and highest activity was observed at 60 °C (up to ~106 g?mol?1?h?1). Most importantly, the catalysts were also effective for the copolymerization of ethylene and 5-hexenyl acetate with moderate activity (~105 g?mol?1?h?1). The microstructure analyses by the 13C NMR spectroscopy indicated that the 5-hexenyl acetate was successfully incorporated into the polyethylene main chain with reasonable comonomer content.