30456-56-5

Basic information

• Product Name: 2-methyl-5-(p-tolyl)pyridine
• Synonyms: 2-methyl-5-(p-tolyl)pyridine
• CAS NO: 30456-56-5
• Molecular Weight: 183.253
• Mol File: 30456-56-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-methyl-5-(p-tolyl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-5-(p-tolyl)pyridine(30456-56-5)
• EPA Substance Registry System: 2-methyl-5-(p-tolyl)pyridine(30456-56-5)

Safety Data

• Hazardous Substances Data: 30456-56-5(Hazardous Substances Data)

Upstream product

• 106-38-7 para-bromotoluene 
• 659742-21-9 (6-methylpyridin-3-yl)boronic acid 
• 116571-06-3 potassium 6-methylnicotinate 
• 3430-13-5 5-bromo-2-methylpyridine 
• 5720-05-8 4-methylphenylboronic acid 

Downstream Products

• 1062229-47-3 (S)-2-(cyclohex-2-enylmethyl)-5-p-tolylpyridine 
• 1311151-52-6 C₁₃H₁₃NO 
• 1311151-83-3 C₁₃H₁₃NO 

Relevant articles and documents

Organic electrode material and preparation method and application thereof

The invention relates to an organic electrode material and a preparation method and application thereof, and belongs to the technical field of materials. The organic electrode material belongs to conjugated carboxylate. The material is used as a working electrode of a sodium ion battery, the specific discharge capacities of an organic electrode material I-1 and an organic electrode material I-2 are 171mAh. g and 184mAh.g respectively after 100 cycles at the current density of 100mA/g, and half batteries prepared by taking I-1 and I-2 as the electrode materials can provide high specific capacity of 119mAh/g and 90mAh/g respectively in a voltage platform test process when 5C is 935mA/g. And the working voltages of the two materials both are between 0.4V and 0.7 V. The electrodematerial prepared by the method can be well applied to the sodium-ion battery, and has excellent oxidation-reduction capability and cycling stability when used as a negative electrode material. The organic electrode material is simple in preparation process and low in cost, and meets the requirement of large-scale preparation.

Palladium-catalyzed decarboxylative cross-coupling of 3-pyridyl and 4-pyridyl carboxylates with aryl bromides

Decarboxylative cross-coupling of 3-pyridyl and 4-pyridyl carboxylates with aryl bromides is reported. Using a bimetallic system of Cu2O and Pd(PPh3)4, the scope of the reaction is demonstrated by the synthesis of 27 pyridine-containing biaryls in moderate to good yields.

Experimental and computational probes of a self-assembled capsule

This research was undertaken to explore the interior surface of a synthetic receptor 1.1 with arylpyridines as guests. The interior surface differentiates the guests through the recognition of their nitrogen atoms. Experimental and computational analyses revealed that there is a delicate balance of attractions and repulsions between the host and the lone pairs of guests.