10477-94-8

Basic information

• Product Name: 3-METHYL-5-PHENYLPYRIDINE
• Synonyms: 3-METHYL-5-PHENYLPYRIDINE;Methylphenylpyridine;3-METHYL-5-PHENYLPYRIDINE 95+%
• CAS NO: 10477-94-8
• Molecular Formula: C₁₂H₁₁N
• Molecular Weight: 169.22
• Mol File: 10477-94-8.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 160°C 14mm
• Flash Point: 123.1°C
• Appearance: /
• Density: 1,07 g/cm3
• Vapor Pressure: 0.00345mmHg at 25°C
• Refractive Index: 1.6060-1.6080
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 5.14±0.20(Predicted)
• CAS DataBase Reference: 3-METHYL-5-PHENYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHYL-5-PHENYLPYRIDINE(10477-94-8)
• EPA Substance Registry System: 3-METHYL-5-PHENYLPYRIDINE(10477-94-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 10477-94-8(Hazardous Substances Data)

Usage

General Description

3-Methyl-5-phenylpyridine is a chemical compound with formula C12H11N. The compound is categorized under the 'pyridines and derivatives' subclass, and belongs to the organic compounds known as arylpyridines. These are compounds containing a pyridine ring substituted at one or more positions by an aryl group. 3-Methyl-5-phenylpyridine is generally used in scientific research and may be utilized in the synthesis of other chemicals. It is light sensitive and should be stored under ambient temperatures. Detailed information about its physical and chemical properties, safety measures, and toxicity can be found in corresponding safety data sheets. As with any chemical, its handling and disposal should adhere to local regulations and guidelines.

InChI:InChI=1/C12H11N/c1-10-7-12(9-13-8-10)11-5-3-2-4-6-11/h2-9H,1H3

Upstream product

• 536-74-3 phenylacetylene 
• 13654-20-1 2-phenyl-penta-2,4-dienenitrile 
• 13633-26-6 4-phenylbut-1-en-3-yne 
• 1585185-86-9 C₁₉H₁₈INO₂S 
• 1585185-79-0 C₁₉H₁₈INO₂S 
• 1585185-72-3 C₂₂H₂₅NO₃S 
• 108-99-6 3-Methylpyridine 
• 591-50-4 iodobenzene 
• 3430-19-1 5-methylpyridin-3-amine 
• 73183-34-3 bis(pinacol)diborane 
• 1379538-73-4 N-(2-methylallyl)-N-tert-butoxycarbonyl-phenylethynylamine 
• 3430-16-8 5-bromo-3-picoline 
• 98-80-6 phenylboronic acid 
• 122-78-1 phenylacetaldehyde 

Downstream Products

• 280135-00-4 4-formyl-1-[(5-phenyl-3-pyridinyl)methyl]-indole 
• 10177-12-5 5-phenylnicotinic acid 

Relevant articles and documents

Direct access to pentenedinitriles: Via Ni-catalyzed dihydrocyanation of 1,3-enynes

A highly regio-and stereoselective dihydrocyanation of 1,3-enynes was implemented by nickel/diphosphine catalysts. This reaction represents the first example of Ni-catalyzed dihydrocyanation of 1,3-enynes using TMSCN and MeOH as HCN surrogates. In this tr

Palladium-catalyzed cyclization of vinyl iodide-tethered allensulfonamide

This Letter describes a palladium-catalyzed cyclization of vinyl iodide-tethered allensulfonamide in the presence of alkylol, which provides a facile access to 2-alkoxy-3-methylene-tetrahydropyridine. The asymmetric version of this reaction has also been preliminarily realized with up to 81% enantioselectivity when chiral bisphosphine ligands were used.

Synthesis of pinacol arylboronates from aromatic amines: A metal-free transformation

A metal-free borylation process based on Sandmeyer-type transformation using arylamines derivatives as the substrates has been developed. Through optimization of the reaction conditions, this novel conversion can be successfully applied to a wide range of aromatic amines, affording borylation products in moderate to good yields. Various functionalized arylboronates, which are difficult to access by other methods, can be easily obtained with this metal-free transformation. Moreover, this transformation can be followed by Suzuki-Miyaura cross-coupling without purification of the borylation products, which enhances the practical usefulness of this method. A possible reaction mechanism involving radical species has been proposed.