1214326-04-1

Basic information

• Product Name: 2-methyl-3,3'-bipyridine
• Synonyms: 2-methyl-3,3'-bipyridine
• CAS NO: 1214326-04-1
• Molecular Formula: C₁₁H₁₀N₂
• Molecular Weight: 170.2105
• Mol File: 1214326-04-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-methyl-3,3'-bipyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-3,3'-bipyridine(1214326-04-1)
• EPA Substance Registry System: 2-methyl-3,3'-bipyridine(1214326-04-1)

Safety Data

• Hazardous Substances Data: 1214326-04-1(Hazardous Substances Data)

Usage

General Description

2-methyl-3,3'-bipyridine is a chemical compound with the molecular formula C12H10N2. It is a member of the bipyridine family of compounds, which are commonly used as ligands in coordination chemistry. 2-methyl-3,3'-bipyridine is often used in the synthesis of coordination complexes and as a building block for the preparation of various organic compounds. It has also been studied for its potential applications in the fields of material science and catalysis. The compound has a unique structure due to the two pyridine rings linked together with a methyl group, which gives it distinctive chemical properties and potential reactivity in various chemical reactions.

Upstream product

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Relevant articles and documents

Synthesis of biaryls through a one-pot tandem borylation/Suzuki-Miyaura cross-coupling reaction catalyzed by a palladacycle

The tricyclohexylphosphane adduct of cyclopalladated ferrocenylimine I exhibited high catalytic activity in the one-pot borylation/Suzuki-Miyaura coupling (BSC) reaction with low catalyst loading (2 mol-%). Various biaryls were obtained in good to excellent yields for 37 examples. This process was applied to aryl and heteroaryl halides (Br and Cl) containing a variety of functional groups and did not require an excess amount of phosphane ligand and the addition of the palladium catalyst in the second step. Cyclopalladated ferrocenylimine I exhibited high catalytic activity in the borylation/Suzuki- Miyaura coupling (BSC) reaction with low catalyst loading. Various unsymmetrical biaryls were obtained ingood to excellent yields in one pot. This protocol was applied to aryl and heteroaryl halides (Br and Cl) containing a variety of functional groups without adding catalyst in the second step. Copyright