328062-45-9

Basic information

• Product Name: 6-phenylH-imidazo[1,2-a]pyridine
• Synonyms: 6-phenylH-imidazo[1,2-a]pyridine;6-phenylimidazo[1,2-a]pyridine
• CAS NO: 328062-45-9
• Molecular Formula: C₁₃H₁₀N₂
• Molecular Weight: 194.2319
• Mol File: 328062-45-9.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-phenylH-imidazo[1,2-a]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenylH-imidazo[1,2-a]pyridine(328062-45-9)
• EPA Substance Registry System: 6-phenylH-imidazo[1,2-a]pyridine(328062-45-9)

Safety Data

• Hazardous Substances Data: 328062-45-9(Hazardous Substances Data)

Upstream product

• 6188-23-4 6-bromoimidazo[1,2-a]pyridine 
• 98-80-6 phenylboronic acid 
• 426825-75-4 6-iodoimidazo[1,2-a]pyridine 
• 88511-25-5 2-amino-6-iodopyridine 
• 100-58-3 phenylmagnesium bromide 
• 6188-25-6 6-Chloro-imidazo[1,2-a]pyridine 
• 107-20-0 2-chloroethanal 
• 33421-40-8 5-phenyl-pyridin-2-ylamine 
• 1072-97-5 5-bromo-2-pyridylamine 
• 138888-98-9 N’-(5-bromopyridin-2-yl)-N,N-dimethylformimidamide 
• 1284293-40-8 (6-bromo-1H-imidazo[1,2-a]pyridin-3-yl)(phenyl)methanone 

Downstream Products

• 328062-46-0 3-bromo-6-phenylimidazo[1,2-a]pyridine 

Relevant articles and documents

MTA-Cooperative PRMT5 Inhibitors

The present invention relates to compounds that inhibit Protein Arginine N-Methyl Transferase 5 (PRMT5) activity. In particular, the present invention relates to compounds, pharmaceutical compositions and methods of use, such as methods of treating cancer using the compounds and pharmaceutical compositions of the present invention.

Pd-Catalyzed Tandem Cyclization via C-H Arylation and Acylation for the Construction of Polycyclic Scaffolds

The first Pd-catalyzed tandem cyclization of imidazo[1,2-a]pyridines with 2-chlorobenzaldehydes through C-H arylation and acylation is presented for the efficient synthesis of novel 6H-benzo[b]imidazo[5,1,2-de]quinolizin-6-ones. The direct acylation react

(Hetero)arylation of 6-halogenoimidazo[1,2-a]pyridines differently substituted at C(2): Influence of the 2-substituent on the Suzuki cross-coupling reaction

We previously reported that reactivity towards the Suzuki cross-coupling reaction of 3-iodoimidazo[1,2-a]pyridines substituted at C(2) is largely influenced by the nature of this 2-substituent. Hence, with the aim to expand the scope of this coupling proc