41855-95-2

Basic information

• Product Name: N-[PHENYL(2-PYRIDINYLAMINO)METHYL]-N-(2-PYRIDINYL)AMINE
• Synonyms: PHENYL-N,N-DI(2-PYRIDINYL)METHANEDIAMINE;N-[PHENYL(2-PYRIDINYLAMINO)METHYL]-N-(2-PYRIDINYL)AMINE;1-phenyl-N,N'-bis(pyridin-2-yl)methanediamine
• CAS NO: 41855-95-2
• Molecular Formula: C₁₇H₁₆N₄
• Molecular Weight: 276.34
• Mol File: 41855-95-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-[PHENYL(2-PYRIDINYLAMINO)METHYL]-N-(2-PYRIDINYL)AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-[PHENYL(2-PYRIDINYLAMINO)METHYL]-N-(2-PYRIDINYL)AMINE(41855-95-2)
• EPA Substance Registry System: N-[PHENYL(2-PYRIDINYLAMINO)METHYL]-N-(2-PYRIDINYL)AMINE(41855-95-2)

Safety Data

• Hazardous Substances Data: 41855-95-2(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 100-52-7 benzaldehyde 

Downstream Products

• 71-43-2 benzene 
• 504-29-0 2-aminopyridine 
• 1883-96-1 N-benzylidenepyridin-2-amine 
• 20622-21-3 1,2-diphenyl-2-(2-pyridinylamino)ethanone 

Relevant articles and documents

NHC-Catalyzed Aza-Benzoin Condensation of N, N′-Dipyridin-2-yl Aminals with Aldehydes

α-Amino ketones are useful compounds because of their synthetic utility and bioactivities. After observing the ability of N,N′-dipyridin-2-yl aminals to form imines in situ, the synthesis of α-amino ketones using N,N′-dipyridin-2-yl aminals was proposed.

CONDENSATION REACTIONS BETWEEN AROMATIC ALDEHYDES AND SOME HETEROCYCLIC AROMATIC AMINES

1,1-Diamino derivatives are obtained by means of reactions between 2-aminothiazole and aromatic aldehydes carried out in methanol (and in dimethyl sulphoxide).The reaction of amine with the C=N of imine occurs without catalyst and is an easier process than its addition to C=O.This behaviour is also displayed by a number of aromatic heterocycles and homocyclic amines and may be explained by considering the activating effect of the electron-withdrawing group present in the imine moiety.