56921-85-8

Basic information

• Product Name: 2-(4-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIMIDINE
• Synonyms: 2-(4-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIMIDINE;imidazo[1,2-a]pyrimidine,2-(4-bromophenyl)-;2-(4-Bromo-phenyl)-imidazo[1,2-a] pyrimidine >99%
• CAS NO: 56921-85-8
• Molecular Formula: C₁₂H₈BrN₃
• Molecular Weight: 274.12
• Mol File: 56921-85-8.mol
• Article Data: 14

Chemical Properties

• Melting Point: 279℃
• Appearance: /
• Density: 1.58
• Storage Temp.: 2-8°C
• PKA: 4.47±0.30(Predicted)
• CAS DataBase Reference: 2-(4-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIMIDINE(56921-85-8)
• EPA Substance Registry System: 2-(4-BROMO-PHENYL)-IMIDAZO[1,2-A]PYRIMIDINE(56921-85-8)

Safety Data

• Hazardous Substances Data: 56921-85-8(Hazardous Substances Data)

Usage

General Description

2-(4-Bromo-phenyl)-imidazo[1,2-a]pyrimidine is a chemical compound with the molecular formula C11H7BrN4. It belongs to the class of imidazopyrimidine derivatives and is commonly used in the pharmaceutical industry as a building block for the synthesis of various biologically active compounds. This chemical has potential applications in the development of drugs for the treatment of various diseases, including cancer, inflammation, and infectious diseases. Its unique structure and properties make it a valuable tool for medicinal chemists in their quest to discover new therapeutic agents. Additionally, 2-(4-Bromo-phenyl)-imidazo[1,2-a]pyrimidine may also have applications in other fields such as agrochemicals and materials science.

InChI:InChI=1S/C12H8BrN3/c13-10-4-2-9(3-5-10)11-8-16-7-1-6-14-12(16)15-11/h1-8H

Upstream product

• 109-12-6 2-aminopyrimidine 
• 99-73-0 para-bromophenacyl bromide 
• 875289-82-0 2,4-dinitro-benzenesulfonic acid 2-(4-bromo-phenyl)-2-oxo-ethyl ester 
• 99-90-1 para-bromoacetophenone 
• 98475-05-9 α-tosyloxy-4-bromoacetophenone 

Downstream Products

• 60472-19-7 4-(4-bromophenyl)-1H-imidazol-2-ylamine 
• 143696-99-5 2-(4-Bromo-phenyl)-5,6,7,8-tetrahydro-imidazo[1,2-a]pyrimidine 
• 64454-32-6 2-(4-bromo-phenyl)-3-nitroso-imidazo[1,2-a]pyrimidine 
• 60472-19-7 5-(p-bromophenyl)-2-aminoimidazole 
• 134044-60-3 2-(4-Bromo-phenyl)-3-nitro-imidazo[1,2-a]pyrimidine 
• 134044-61-4 2-(4-Bromo-phenyl)-imidazo[1,2-a]pyrimidin-3-ylamine 

Relevant articles and documents

DIAZABICYCLIC SUBSTITUTED IMIDAZOPYRIMIDINES AND THEIR USE FOR THE TREATMENT OF BREATHING DISORDERS

The present invention relates to novel diazabicyclically substituted imidazo[1,2-a]pyrimidine derivatives, to methods for producing the same, to the use thereof either alone or in combinations for the treatment and/or prevention of diseases, as well as to

Imidazo[1,2-A]pyrimidine-containing compounds, method for preparing the same, and their use in electronic devices

The present disclosure describes novel imidazo[1,2-a]pyrimidine-containing organic light-emitting compounds represented by formula (I): wherein R1 and R2 independently represent hydrogen, an alkyl group, or an aryl group which is uns

Hypervalent iodine(III) sulfonate mediated synthesis of 2-arylimidazo[1,2-a]pyrimidines in liquid PEG-400

PEG-400[poly(ethylene glycol-400)] is used as a "green" recyclable solvent in the one-pot synthesis of 2-arylimidazo[1,2-a]pyrimidines by reaction with ketones, [hydroxyl(2,4-dinitrobenzenesulfonyloxy)-iodo]benzene (HDNIB), and 2-aminopyrimidine. Signific