35070-08-7

Basic information

• Product Name: 2-Methoxy-6-phenylpyridine
• Synonyms: 2-Methoxy-6-phenylpyridine;2-Methoxy-6-phenylpridine
• CAS NO: 35070-08-7
• Molecular Formula: C₁₂H₁₁NO
• Molecular Weight: 185.22
• Mol File: 35070-08-7.mol
• Article Data: 21

Chemical Properties

• Appearance: /
• Storage Temp.: Room temperature.
• CAS DataBase Reference: 2-Methoxy-6-phenylpyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methoxy-6-phenylpyridine(35070-08-7)
• EPA Substance Registry System: 2-Methoxy-6-phenylpyridine(35070-08-7)

Safety Data

• Hazardous Substances Data: 35070-08-7(Hazardous Substances Data)

Usage

General Description

2-Methoxy-6-phenylpyridine is a chemical compound with the molecular formula C13H11NO, which consists of a heterocyclic ring containing a pyridine and a phenyl group, as well as a methoxy group. It is a pale yellow crystalline powder that is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2-Methoxy-6-phenylpyridine has applications in the production of drugs such as antimalarials and antipsychotic medications. It is also used in the manufacture of pesticides and other agricultural chemicals. 2-Methoxy-6-phenylpyridine has potential uses in various fields such as medicine and agriculture due to its unique chemical structure and properties.

Upstream product

• 17228-64-7 6-chloro-2-methoxypyridine 
• 100-59-4 phenylmagnesium chloride 
• 98-80-6 phenylboronic acid 
• 40473-07-2 6-bromo-2-methoxypyridine 
• 100-58-3 phenylmagnesium bromide 
• 108-86-1 bromobenzene 
• 1034297-69-2 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine 
• 960-16-7 tributylphenylstannane 
• 1078-58-6 diphenylzinc 
• 164014-94-2 2-methoxy-6-(tri-n-butylstannyl)pyridine 
• 591-50-4 iodobenzene 
• 1356823-18-1 2-methoxyphenyl N-methyliminodiacetic acid borate 
• 2996-92-1 phenyl trimethylsiloxane 
• 3240-34-4 [bis(acetoxy)iodo]benzene 

Downstream Products

• 19006-82-7 2-hydroxy-6-phenylpyridine 
• 1313359-11-3 2-(2-chlorophenyl)-6-methoxypyridine 
• 1313359-12-4 4-chloro-2-(2-chlorophenyl)-6-methoxypyridine 
• 1313359-13-5 3-chloro-6-(2-chlorophenyl)-2-methoxypyridine 
• 1446325-89-8 C₂₀H₁₄N₂O₃ 
• 1046789-41-6 2-(6-methoxypyridin-2-yl)benzonitrile 
• 19006-82-7 6-phenyl-2-pyridone 
• 1360567-57-2 2-phenyl-6-(piperidin-1-yl)pyridine 

Relevant articles and documents

N-Heterocarbene Palladium Complexes with Dianisole Backbones: Synthesis, Structure, and Catalysis

A series of palladium N-heterocyclic carbenes (NHCs), complexes C1-C5, bearing dianisole backbones and substituted N-aryl moieties have been synthesized and characterized. The electronic effect as well as the steric environment of the NHC ligands has been assessed. The synthesized palladium complexes were applied for Suzuki-Miyaura cross-coupling reactions under aerobic conditions. The relationship between the catalytic structure and catalytic performance was then extensively investigated. Upon optimizing the reaction conditions, the C4 was found to be highly efficient to catalyze the cross-coupling of (hetero)aryl chlorides with (hetero)arylboronic acids at a 0.1 mol % palladium loading.

Insight into Copper Catalysis: In Situ Formed Nano Cu2O in Suzuki-Miyaura Cross-Coupling of Aryl/Indolyl Boronates

A ligand-free copper catalyzed Suzuki-Miyaura coupling of 3,5-diiodopyridine with aryl and indole boronates has been explored in good to excellent yields. In situ generation of nano-Cu2O from CuCl2 under the reaction conditions has been discovered for the first time. The generality of the reaction was further demonstrated by the arylation of 5-iodopyrimidine, iodopyridines, iodobenzenes, and diiodobenzenes and resulted in good to moderate yields. Moreover, bisindole alkaloid Scalaridine A has been successfully synthesized in 60% overall yield.

Pd-Catalyzed Ligand-Free Synthesis of Arylated Heteroaromatics by Coupling of N-Heteroaromatic Bromides with Iodobenzene Diacetate, Iodosobenzene, or Diphenyliodonium Salts

An efficient method for synthesizing arylated heteroaromatics has been reported via Pd-catalyzed ligand-free cross-coupling of N-heteroaromatic bromides with iodine(III) reagents under mild conditions. Iodobenzene diacetate, iodosobenzene, and diphenyliod