278600-44-5

Basic information

• Product Name: 4-Pyridinamine, N,N-diethyl-3-(2-phenyl-1-naphthalenyl)-
• CAS NO: 278600-44-5
• Molecular Formula: C25H24N2
• Molecular Weight: 352.479
• Mol File: 278600-44-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-Pyridinamine, N,N-diethyl-3-(2-phenyl-1-naphthalenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pyridinamine, N,N-diethyl-3-(2-phenyl-1-naphthalenyl)-(278600-44-5)
• EPA Substance Registry System: 4-Pyridinamine, N,N-diethyl-3-(2-phenyl-1-naphthalenyl)-(278600-44-5)

Safety Data

• Hazardous Substances Data: 278600-44-5(Hazardous Substances Data)

Upstream product

• 320381-26-8 (2-phenylnaphthalene-1-yl)boronic acid 
• 612086-24-5 (3-bromopyridin-4-yl)diethylamine 
• 109-89-7 diethylamine 
• 612086-27-8 4-chloro-3-(2-phenyl-naphthalen-1-yl)pyridine 
• 278600-41-2 diethyl{3-[2-(phenylmethoxy)naphthyl](4-pyridyl)}-amine 
• 278600-42-3 1-[4-(diethylamino)pyridin-3-yl]naphthalen-2-ol 
• 28419-11-6 3,5-dibromo-1,4-dihydropyridin-4-one 
• 13626-17-0 3,5-dibromo-4-chloro-pyridine 
• 108-96-3 4-pyridone 
• 612086-26-7 (+/-)-3-bromo-4-chloro-5-(2-phenylnaphthalen-1-yl)pyridine 
• 612086-25-6 4,4,5,5-tetramethyl-2-(2-phenyl-naphthalen-1-yl)-[1,3,2]dioxaborolane 
• 278600-40-1 (3,5-dibromopyridin-4-yl)diethylamine 
• 126613-08-9 trifluoromethanesulfonic acid 1-bromonaphthalen-2-yl ester 
• 22082-93-5 1-bromo-2-phenylnaphthalene 

Relevant articles and documents

PROCESS FOR THE PREPARATION OF ATROPISOMERIC ANALOGUES OF 4-AMINOPYRIDINE

The present invention relates to a process for the preparation of 3,4-disubstituted pyridines from commercially available starting materials. In particular, the invention relates to the process for the preparation for a compound of formula (I) wherein a c

Concise synthesis, preparative resolution, absolute configuration determination, and applications of an atropisomeric biaryl catalyst for asymmetric acylation

A new three-step synthesis and resolution of nucleophilic catalyst 1 suitable for large-scale preparation has been developed, and this catalyst has been shown to be effective for the kinetic resolution and asymmetric desymmetrization of a range of sec-alcohol substrates.