13959-34-7

Basic information

• Product Name: 4-METHYL-2-VINYL-PYRIDINE
• Synonyms: 4-METHYL-2-VINYL-PYRIDINE
• CAS NO: 13959-34-7
• Molecular Formula: C₈H₉N
• Molecular Weight: 119.16376
• Mol File: 13959-34-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• CAS DataBase Reference: 4-METHYL-2-VINYL-PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHYL-2-VINYL-PYRIDINE(13959-34-7)
• EPA Substance Registry System: 4-METHYL-2-VINYL-PYRIDINE(13959-34-7)

Safety Data

• Hazardous Substances Data: 13959-34-7(Hazardous Substances Data)

Usage

General Description

4-Methyl-2-vinylpyridine is a chemical compound with the molecular formula C9H9N. It is a colorless to pale yellow liquid that is commonly used in the production of polymers, resins, and coatings. It is also utilized as a monomer in the synthesis of specialty polymers and copolymers. 4-Methyl-2-vinylpyridine is a highly reactive compound with a strong odor and is considered to be a flammable liquid. It is important to handle this chemical with caution and ensure proper ventilation and protective equipment when working with it. This chemical is primarily used in industrial processes and is not commonly found in consumer products.

Upstream product

• 4664-18-0 2-(4-methyl-pyridin-2-yl)-ethanol 
• 108-47-4 2,4-lutidine 
• 4926-28-7 2-Bromo-4-picoline 
• 7486-35-3 tri-n-butyl(vinyl)tin 
• 53547-60-7 4-methyl-2-pyridinecarbaldehyde 
• 2065-66-9 methyl-triphenylphosphonium iodide 

Downstream Products

• 71858-92-9 2-(2-Cyanethyl)-4-methylpyridin 
• 132554-31-5 1,4-Dimethyl-2-(2-benzoylethyl)pyridinium iodide 
• 132554-27-9 3-(4-Methyl-pyridin-2-yl)-1-phenyl-propan-1-one 
• 100710-97-2 2-(2-benzenesulfonyl-ethyl)-4-methyl-pyridine 
• 106320-21-2 4-methyl-2-(2-phenylsulfanyl-ethyl)-pyridine 

Relevant articles and documents

Cobalt-catalyzed addition of styrylboronic acids to 2-vinylpyridine derivatives

Treatment of 2-vinyl nitrogen-containing heteroaromatic compounds with styrylboronic acid in the presence of a cobalt catalyst and a base results in an addition reaction to afford the corresponding 4-phenyl-3-butenyl heteroarenes. The adjacent nitrogen atom is essential for the promotion of the reaction because the nitrogen accelerates the addition of the styryl cobalt species, generated by transmetalation, onto the vinyl group. The reaction represents a rare example of cobalt catalysis in the reactions of organoboronic acids. Accelerated addition: Treatment of 2-vinylpyridine derivatives with styrylboronic acids under cobalt catalysis results in addition reactions. This represents a rare example of the cobalt-catalyzed reaction of organoboronic acids. Cobalt shows catalytic activity similar to rhodium, and catalyzes an unprecedented assembly of organoboronic acids and activated alkenes. Copyright