874306-45-3

Basic information

• Product Name: N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)-3-([(3β,5β,17α,20S)-24-{3-[(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)amino]phenoxy}cholan-3-yl]oxy)aniline
• Synonyms: N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)-3-([(3β,5β,17α,20S)-24-{3-[(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)amino]phenoxy}cholan-3-yl]oxy)aniline
• CAS NO: 874306-45-3
• Molecular Weight: 951.384
• Mol File: 874306-45-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)-3-([(3β,5β,17α,20S)-24-{3-[(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)amino]phenoxy}cholan-3-yl]oxy)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)-3-([(3β,5β,17α,20S)-24-{3-[(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)amino]phenoxy}cholan-3-yl]oxy)aniline(874306-45-3)
• EPA Substance Registry System: N-(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)-3-([(3β,5β,17α,20S)-24-{3-[(3-{2-[2-(3-aminopropoxy)ethoxy]ethoxy}propyl)amino]phenoxy}cholan-3-yl]oxy)aniline(874306-45-3)

Safety Data

• Hazardous Substances Data: 874306-45-3(Hazardous Substances Data)

Upstream product

• 434-13-9 Lithocholic acid 
• 20414-15-7 5β-cholane-3α,24-diol 
• 874306-27-1 (3α,5β)-24-(3-bromophenoxy)cholan-3-ol 
• 874306-28-2 (3α,5β)-3,24-bis(3-bromophenoxy)cholane 
• 4246-51-9 4,7,10-trioxa-1,13-diaminotridecane 

Relevant articles and documents

Palladium-catalyzed amination in the synthesis and modification of acyclic oxadiamino cholane derivatives

Palladium-catalyzed reactions of 24-(haloaryloxy)cholanes and 3,24-bis(haloaryloxy)cholanes with excess oxadiamines gave the corresponding mono- and bis(oxadiamino)-substituted cholanes which were subjected to palladium-catalyzed arylation with 1,3-dibrom

Synthesis of nitrogen- and oxygen-containing macrocycles - Derivatives of lithocholic acid

Palladium-catalyzed amination of 3,24-bis(3-bromophenoxy)cholane (4) with various polyamines and polyoxadiamines 5 taken in 1:1 ratio was used for the synthesis of the macrocycles 6, which contain steroidal and polyamine moieties and were obtained in 38-6