19087-55-9

Basic information

• Product Name: 2-(2-PYRIDIN-2-YL-VINYL)-PHENOL
• Synonyms: 2-(2-PYRIDIN-2-YL-VINYL)-PHENOL;ALPHA-(2-PYRIDYLMETHYLENE)-O-CRESOL;2-[(E)-2-pyridin-2-ylvinyl]phenol
• CAS NO: 19087-55-9
• Molecular Formula: C₁₃H₁₁NO
• Molecular Weight: 197.23
• Mol File: 19087-55-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-PYRIDIN-2-YL-VINYL)-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-PYRIDIN-2-YL-VINYL)-PHENOL(19087-55-9)
• EPA Substance Registry System: 2-(2-PYRIDIN-2-YL-VINYL)-PHENOL(19087-55-9)

Safety Data

• Hazardous Substances Data: 19087-55-9(Hazardous Substances Data)

Usage

Type of Compound

Organic compound

Main Components

Phenol group, vinyl group, pyridine ring

Usage

Synthesis of pharmaceuticals, agrochemicals, and various organic compounds

Applications

Development of materials with specific properties, production of dyes, and other organic chemicals

Suitability

Various applications in organic chemistry and material science

Molecular Structure

The presence of a phenol group with a vinyl group attached to a pyridine ring contributes to its versatility and potential applications.

Upstream product

• 109-06-8 α-picoline 
• 90-02-8 salicylaldehyde 
• 100-69-6 2-vinylpyridine 
• 533-58-4 2-Iodophenol 
• 23560-36-3 (E)-2-[2-(pyridin-2-yl)vinyl]phenyl acetate 

Downstream Products

• 56920-35-5 2-<β-(4'-Hydroxyphenyl)-ethyl>-pyridin 
• 7035-05-4 2-(benzofuran-2-yl)pyridine 

Relevant articles and documents

Anti-Angiogenic Compounds

Compounds and compositions are described which are useful especially for treatment of angiogenesis-related diseases or disorders such as neovascularisation of the eye, age-related macular degeneration, diabetic retinopathy or cancer.

Lewis-acid-catalyzed benzylic reactions of 2-methylazaarenes with aldehydes

Lewis-acid-catalyzed benzylic reactions of 2-methylazaarenes with aldehydes have been investigated. Series of azaarene derivatives were afforded by this reaction. 2-(Pyridin-2-yl)ethanols with common substituents were formed through the LiNTf2-promoted aldol reaction for the first time. 2-Alkenylpyridines, exclusively in the form of the E isomers, were synthesized in the presence of LiNTf2 cooperated with H2NTf. In the presence of La(Pfb)3 as catalysis, 2-alkenylquinolines were obtained in high yields through the reactions between 2-methylquinolines and aldehydes under air.