13362-75-9

Usage

Uses

Used in Organic Synthesis:
(E)-2-[2-(3-pyridyl)vinyl]pyridine is used as a building block for the synthesis of complex organic molecules. Its presence in the molecular structure allows for the creation of a wide range of compounds with diverse properties and potential applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (E)-2-[2-(3-pyridyl)vinyl]pyridine is used as a key component in the development of new drugs. Its unique chemical properties enable the design and synthesis of novel therapeutic agents with potential applications in various medical fields.
Used in Coordination Chemistry:
(E)-2-[2-(3-pyridyl)vinyl]pyridine is used as a ligand in coordination chemistry, where it forms complexes with metal ions. These complexes have potential applications in catalysis, materials science, and as models for understanding biological processes.
Used as a Precursor for Synthesis:
(E)-2-[2-(3-pyridyl)vinyl]pyridine serves as a precursor for the synthesis of various organic compounds, contributing to the development of new materials and chemicals with specific properties and functions.

InChI:InChI=1/C12H10N2/c1-2-9-14-12(5-1)7-6-11-4-3-8-13-10-11/h1-10H/b7-6+

Upstream product

• 10299-54-4 2-[2]pyridyl-1-[3]pyridyl-ethanol 
• 109-06-8 α-picoline 
• 614-18-6 3-pyridinecarboxylic acid ethyl ester 
• 59576-33-9 2-(2-pyridinyl)-1-(3-pyridinyl)ethanone 
• 100-69-6 2-vinylpyridine 
• 626-55-1 3-Bromopyridine 

Downstream Products

• 14802-38-1 cis-1-[2]Pyridyl-2-[3]pyridyl-aethen 

Relevant academic research and scientific papers

Palladium- meta -terarylphosphine catalyst for the Mizoroki-Heck reaction of (hetero)aryl bromides and functional olefins

The evolutionary meta-terarylphosphine ligand architecture of Cy?Phine was recently shown to be a key feature that imposed outstanding performance in palladium-catalyzed copper-free Sonogashira applications. Herein, the Pd-Cy?Phine combination has similar

Can Palladium Acetate Lose Its "saltiness"? Catalytic Activities of the Impurities in Palladium Acetate

Commercially available palladium acetate often contains two major impurities, whose presence can impact the overall catalytic efficacy. This systematic study provides a comparison of the differences in catalytic activity of pure palladium acetate, Pd3(OAc)6, with the two impurities: Pd3(OAc)5(NO2) and polymeric [Pd(OAc)2]n in a variety of cross-coupling reactions. The solid state 13C NMR spectra of all three compounds in conjunction with DFT calculations confirm their reported geometries.

Heck cross-coupling of vinyl heteroaromatic compounds with aryl and heteroaryl halides using Pd(II) complex under phosphine-free conditions

The palladium-catalyzed cross-coupling reaction of vinyl heteroaromatic compounds with aryl bromides and heteroaryl bromides is described using air and moisture stable N,N′,N″,O-tetrafunctional Pd catalyst under phosphine-free conditions. As a result a variety of trans-1,2-disubstituted vinyl heterocycles were obtained in high to good yields.

Utilities of olefin derivatives

Compounds having an activity to enhance the expression of apoAI are provided. Compounds of formula (I): in which Ar1 and Ar2 are independently a phenyl, naphthyl, or monocyclic or bicyclic aromatic heterocyclic group, which may be optionally substituted; —X— is —N═CZ2-, —CY2═CZ2-, —CY2Y3—CHZ2-, —S—, —O—, or the like; Y1, Y2, Y3, Z1 and Z2 are independently a hydrogen, a halogen, a lower alkyl, a phenyl, or the like; Z1 and Z2 may be independently a linker group that may combine with Ar2 and Ar1 to form a condensed ring; m is 0 or 1, and n is 0 to 2; a prodrug thereof, a pharmaceutically acceptable salt or solvate of them; are disclosed.