74037-48-2

Basic information

• Product Name: N-(2-Pyridyl)-1,2-diphenylethanamine
• Synonyms: 2-(1,2-Diphenylethylamino)pyridine;N-(2-Pyridyl)-1,2-diphenylethanamine;N-(1,2-diphenylethyl)pyridin-2-amine
• CAS NO: 74037-48-2
• Molecular Formula: C₁₉H₁₈N₂
• Molecular Weight: 274.3596
• Mol File: 74037-48-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 428.3°Cat760mmHg
• Flash Point: 212.9°C
• Appearance: /
• Density: 1.139g/cm³
• Vapor Pressure: 1.53E-07mmHg at 25°C
• Refractive Index: 1.647
• CAS DataBase Reference: N-(2-Pyridyl)-1,2-diphenylethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Pyridyl)-1,2-diphenylethanamine(74037-48-2)
• EPA Substance Registry System: N-(2-Pyridyl)-1,2-diphenylethanamine(74037-48-2)

Safety Data

• Hazardous Substances Data: 74037-48-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C19H18N2/c1-3-9-16(10-4-1)15-18(17-11-5-2-6-12-17)21-19-13-7-8-14-20-19/h1-14,18H,15H2,(H,20,21)

Upstream product

• 1883-96-1 N-benzylidenepyridin-2-amine 
• 6921-34-2 benzylmagnesium chloride 
• 4589-12-2 N-(pyrid-2-yl)benzamide 
• 96354-74-4 N-(diphenylmethyl)pyridin-2-amine 
• 5223-01-8 2-phenyl-N-(pyridin-2-yl)acetamide 
• 5123-13-7 5,5-dimethyl-2-phenyl-1,3,2-dioxaborinane 
• 13606-95-6 N-(pyridin-2-yl)butyramide 
• 923748-45-2 N-(pyridin-2-yl)monomethyl terephthalate monoamide 
• 103-80-0 phenylacetyl chloride 
• 504-29-0 2-aminopyridine 

Downstream Products

• 504-29-0 2-aminopyridine 
• 4714-14-1 Chloro-1 diphenyl-1,2 ethane 
• 14547-82-1 4-chloro-N-(pyridine-2-yl)benzamide 
• 59898-94-1 N-(pyridin-2-yl)isonicotinamide 
• 86847-59-8 2-(pivaloylamino)pyridine 
• 51484-40-3 N-pyridin-2-yl(1,1'-biphenyl)-4-acetamide 

Relevant articles and documents

Ruthenium-Catalyzed Reductive Arylation of N-(2-Pyridinyl)amides with Isopropanol and Arylboronate Esters

A new three-component reductive arylation of amides with stable reactants (iPrOH and arylboronate esters), making use of a 2-pyridinyl (Py) directing group, is described. The N-Py-amide substrates are readily prepared from carboxylic acids and PyNH2, and the resulting N-Py-1-arylalkanamine reaction products are easily transformed into the corresponding chlorides by substitution of the HN-Py group with HCl. The 1-aryl-1-chloroalkane products allow substitution and cross-coupling reactions. Therefore, a general protocol for the transformation of carboxylic acids into a variety of functionalities is obtained. The Py-NH2 by-product can be recycled.