99984-63-1

Basic information

• Product Name: 2-methoxy-3-phenylpyrazine
• Synonyms: 2-methoxy-3-phenylpyrazine
• CAS NO: 99984-63-1
• Molecular Weight: 186.213
• Mol File: 99984-63-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-methoxy-3-phenylpyrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-3-phenylpyrazine(99984-63-1)
• EPA Substance Registry System: 2-methoxy-3-phenylpyrazine(99984-63-1)

Safety Data

• Hazardous Substances Data: 99984-63-1(Hazardous Substances Data)

Upstream product

• 3149-28-8 2-methoxypyrazine 
• 591-51-5 phenyllithium 
• 108-90-7 chlorobenzene 
• 2882-18-0 3-phenyl-2(1H)-pyrazinone 
• 41270-65-9 2-chloro-3-phenylpyrazine 
• 124-41-4 sodium methylate 
• 99984-69-7 3-methoxy-2-phenyl-pyrazine-1-oxide 

Downstream Products

• 99984-69-7 3-methoxy-2-phenyl-pyrazine-1-oxide 
• 64163-09-3 2,5-dichloro-6-phenylpyrazine 
• 64163-16-2 5-chloro-6-phenyl-1H-pyrazin-2-one 
• 102653-50-9 5-chloro-3-phenyl-2(1H)-pyrazinone 
• 104092-52-6 5-chloro-2-methoxy-3-phenyl-pyrazine 
• 860410-57-7 2-chloro-5-methoxy-3-phenylpyrazine 
• 100142-71-0 2,5-dimethoxy-3-phenyl-pyrazine 
• 98948-89-1 3-bromo-5-chloro-6-phenyl-1H-pyrazin-2-one 
• 74134-66-0 5-chloro-3,6-diphenyl-1H-pyrazin-2-one 
• 1094461-31-0 2-phenyl-3-methoxy-5-methylpyrazine 

Relevant articles and documents

Base-mediated intermolecular sp2 C-H bond arylation via benzyne intermediates

A transition-metal-free method for arylation of heterocycle and arene carbon-hydrogen bonds by aryl chlorides and fluorides has been developed. The reactions proceed via aryne intermediates and are highly regioselective with respect to the C-H bond coupling component.

Studies on Pyrazines. Part 27. A New Deoxidative Nucleophilic Substitution of Pyrazine N-Oxides; Synthesis of Azidopyrazines with Trimethylsilyl Azide

Azidopyrazines bearing amino, methoxy and/or phenylgroups have been synthesized by reaction of pyrazine N-oxides with trimethylsilyl azide in the presence of diethylcarbamoyl chloride in refluxing acetonitrile.In most cases, the azidation occurs only at t