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

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

Uses

Used in Polymer Production:
4-METHYL-2-VINYL-PYRIDINE is used as a monomer for the production of polymers, contributing to the formation of various types of polymers with specific properties. Its reactivity allows it to be easily incorporated into polymer chains, enhancing their characteristics.
Used in Resin and Coating Industries:
In the resin and coating industries, 4-METHYL-2-VINYL-PYRIDINE is used as a key component in the synthesis of resins and coatings. Its incorporation into these materials can improve their durability, adhesion, and resistance to environmental factors.
Used in Specialty Polymers and Copolymers:
4-METHYL-2-VINYL-PYRIDINE is also utilized as a monomer in the synthesis of specialty polymers and copolymers. These materials are designed for specific applications, such as high-temperature resistance, chemical resistance, or improved mechanical properties, and are used across various industries.

Upstream product

• 4664-18-0 2-(4-methyl-pyridin-2-yl)-ethanol 
• 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 
• 108-47-4 2,4-lutidine 

Downstream Products

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

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

2-(1H-INDAZOL-6-YLAMINO)-BENZAMIDE COMPOUNDS AS PROTEIN KINASES INHIBITORS USEFUL FOR THE TREATMENT OF OPHTALMIC DISEASES

Indazole compounds that modulate and/or inhibit the ophthalmic diseases and the activity of certain protein kinases are described. These compounds and pharmaceutical compositions containing them are capable of mediating tyrosine kinase signal transduction and thereby modulate and/or inhibit unwanted cell proliferation. The invention is also directed to the therapeutic or prophylactic use of pharmaceutical compositions containing such compounds, and to methods of treating ophthalmic diseases and cancer and other disease states associated with unwanted angiogenesis and/or cellular proliferation, such as diabetic retinopathy, neovascular glaucoma,rheumatoid arthritis, and psoriasis, by administering effective amounts of such compounds.