15764-47-3

Basic information

• Product Name: 2-PHENYLIMIDAZO[1,2-A]PYRIMIDINE
• Synonyms: 2-PHENYLIMIDAZO[1,2-A]PYRIMIDINE
• CAS NO: 15764-47-3
• Molecular Formula: C₁₂H₉N₃
• Molecular Weight: 195.22
• Mol File: 15764-47-3.mol
• Article Data: 26

Chemical Properties

• Melting Point: 196-197 °C
• Appearance: /
• Density: 1.21±0.1 g/cm3(Predicted)
• PKA: 4.68±0.30(Predicted)
• CAS DataBase Reference: 2-PHENYLIMIDAZO[1,2-A]PYRIMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENYLIMIDAZO[1,2-A]PYRIMIDINE(15764-47-3)
• EPA Substance Registry System: 2-PHENYLIMIDAZO[1,2-A]PYRIMIDINE(15764-47-3)

Safety Data

• Hazardous Substances Data: 15764-47-3(Hazardous Substances Data)

Upstream product

• 109-12-6 2-aminopyrimidine 
• 79069-32-2 phenyl(phenylethynyl)iodonium tosylate 
• 1310-73-2 sodium hydroxide 
• 70-11-1 α-bromoacetophenone 
• 4636-16-2 iodoacetophenone 
• 20718-17-6 2-(dimethyl(oxo)-λ⁶-sulfaneylidene)-1-phenylethan-1-one 
• 98-88-4 benzoyl chloride 
• 389614-52-2 α-[(2,4-dinitrobenzene)sulfonyl]oxyacetophenone 
• 98-86-2 acetophenone 
• 7257-94-5 1-phenyl-2-(p-tolylsulfonyloxy)ethanone 
• 64-17-5 ethanol 

Downstream Products

• 371234-15-0 2-phenyl-3-(phenylthio)imidazo[1,2-a]pyrimidine 
• 74944-29-9 2-Phenylimidazo<1,2-a>pyrimidin-3-carboxaldehyd 
• 1449488-39-4 3-(methylthio)-2-phenylimidazo[1,2-a]pyrimidine 
• 1310492-93-3 2-phenyl-3-(phenylselanyl)imidazo[1,2-a]pyrimidine 
• 909104-05-8 3-(4-(trifluoromethyl)phenyl)-2-phenylimidazo[1,2-a]pyrimidine 
• 1259389-29-1 5-(4-(trifluoromethyl)phenyl)-2-isobutylthiazole 
• 1259389-30-4 3-(4-(trifluoromethyl)phenyl)-2-methylindolizine 
• 6775-40-2 5-phenyl-2-amino-1H-imidazole 

Relevant articles and documents

Facile access to novel 3-acylimidazo[1,2-a]pyrimidines under microwave irradiation

Treatment of mono-, bis- and tris(ω-bromoacetophenone) derivatives with N,N-dimethylformamidine derivative of 2-aminopyrimidine, afforded the novel 3-aroyl or heteroyl derivatives of imidazo[1,2-α]pyrimidine, bis(imidazo[1,2-α]pyrimidine) and tris(imidazo

Hypervalent Iodine in Synthesis 93. A Facile Synthesis of 2-Substituted Imidazo[1,2-a]pyrimidines by Cyclocondensation of Alkynyl(phenyl)iodonium Salts and 2-Aminopyrimidine

Simple stirring of a mixture of the alkynyl(phenyl)iodonium salts 1 with 2-aminopyrimidine 2 in chloroform under reflux for two hours in the presence of K2CO3 gave, after workup, the 2-substituted imidazo[1,2-a]pyrimidines 3 in moderate to good yields. A possible mechanism for the formation of 3 involves the intramolecular cyclization of the intermediate alkylidenecarbene 6.

Metal complex and application thereof

The invention relates to a metal complex and application thereof, the metal complex is a metal complex electrophosphorescent luminescent material with a pyrimidine fused ring structure, and is a series of metal complexes obtained by taking modified pyrimi

Cobalt-Catalyzed Aerobic Cross-Dehydrogenative Coupling of C-H and Thiols in Water for C-S Formation

Organosulfides have great significance and value in synthetic and biological chemistry. To establish a versatile and green methodology for C-S bond generation, we successfully developed a new aerobic cross-dehydrogenative coupling of C-H and S-H to synthe

Easy and efficient selenocyanation of imidazoheterocycles using triselenodicyanide

The regioselective selenocyanation of imidazoheterocycles using triselenodicyanide at room temperature is reported. The electrophilic aromatic substitution of a broad range of substrates is promoted by the triselenodicyanide obtained by oxidative coupling