31555-35-8

Basic information

• Product Name: 4-IMIDAZO[1,2-A]PYRIMIDIN-2-YLPHENYL METHYL ETHER
• Synonyms: 2-(4-METHOXY-PHENYL)-IMIDAZO[1,2-A]PYRIMIDINE;4-IMIDAZO[1,2-A]PYRIMIDIN-2-YLPHENYL METHYL ETHER
• CAS NO: 31555-35-8
• Molecular Formula: C₁₃H₁₁N₃O
• Molecular Weight: 225.25
• Mol File: 31555-35-8.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-IMIDAZO[1,2-A]PYRIMIDIN-2-YLPHENYL METHYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-IMIDAZO[1,2-A]PYRIMIDIN-2-YLPHENYL METHYL ETHER(31555-35-8)
• EPA Substance Registry System: 4-IMIDAZO[1,2-A]PYRIMIDIN-2-YLPHENYL METHYL ETHER(31555-35-8)

Safety Data

• Hazardous Substances Data: 31555-35-8(Hazardous Substances Data)

Upstream product

• 109-12-6 2-aminopyrimidine 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 875289-81-9 2,4-dinitro-benzenesulfonic acid 2-(4-methoxy-phenyl)-2-oxo-ethyl ester 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 123466-30-8 [(4-methoxyphenyl)ethynyl](phenyl)iodonium tosylate 

Downstream Products

• 134044-65-8 2-(4-Methoxy-phenyl)-5,6,7,8-tetrahydro-imidazo[1,2-a]pyrimidine 
• 30469-01-3 2-(4-methoxy-phenyl)-3-nitroso-imidazo[1,2-a]pyrimidine 
• 60472-20-0 5-(4-methoxyphenyl)-1H-imidazol-2-ylamine 
• 500228-75-1 2-(4-methoxyphenyl)imidazo[1,2-a]pyrimidine-3-carbaldehyde 
• 1186493-20-8 3-benzyl-2-(4-methoxyphenyl)imidazo[1,2-a]pyrimidine 
• 60472-20-0 4-(4-methoxyphenyl)-1H-imidazol-2-ylamine 
• 909104-18-3 3-(4-chlorophenyl)-2-(4-methoxyphenyl)imidazo[1,2-a]pyrimidine 
• 909104-20-7 3-(2-fluorophenyl)-2-(4-methoxyphenyl)imidazo[1,2-a]pyrimidine 

Relevant articles and documents

Synthesis and anti-inflammatory activity of 1,2-3-substituted 2a1,4,5-triazacyclopenta[cd]indene derivatives

The present study reports the synthesis of 1,2-3-substituted-2a1,4,5-triazacyclopenta[cd]indene derivatives. The synthetic methodology includes some of the prominent reaction steps as specified in sequence (i) Bromination of acetophenones (ii) Condensation of 2-bromo-1-(substituted phenyl) ethanone derivatives with 2-aminopyrimidine, and (iii) Coupling of imidazo[1,2-a]pyrimidine derivatives with 1,2-diaryl/diaklylethynes. The structures of the newly synthesized derivatives have been determined by 1H NMR, 13C NMR, LC-MS, and IR spectral analysis. Furthermore, these derivatives were screened for their preliminary anti-inflammatory activities using Carrageenan induced paw edema test method. These promising screening results suggested a huge potential for the molecular diversity from present compounds that can be inflated to better lead candidates.

Efficient Access to Imidazo[1,2- a] pyridines/pyrazines/pyrimidines via Catalyst-Free Annulation Reaction under Microwave Irradiation in Green Solvent

An expeditious catalyst-free heteroannulation reaction for imidazo[1,2-a]pyridines/pyrimidines/pyrazines was developed in green solvent under microwave irradiation. Using H2O-IPA as the reaction medium, various substituted 2-aminopyridines/pyra

Structure-activity relationship of 4(5)-aryl-2-amino-1 H -imidazoles, N 1-substituted 2-aminoimidazoles and imidazo[1,2- a ]pyrimidinium salts as inhibitors of biofilm formation by salmonella typhimurium and pseudomonas aeruginosa

A library of 112 4(5)-aryl-2-amino-1H-imidazoles, 4,5-diphenyl-2-amino-1H- imidazoles, and N1-substituted 4(5)-phenyl-2-aminoimidazoles was synthesized and tested for the antagonistic effect against biofilm formation by Salmonella Typhimurium and Pseudomo