312908-82-0

Basic information

• Product Name: 1,5,9,13-Tetraazacycloheptadecan-6-one, 8-(4-hydroxyphenyl)-1-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-, (8S)-
• CAS NO: 312908-82-0
• Molecular Formula: C28H38N4O4
• Molecular Weight: 494.634
• Mol File: 312908-82-0.mol

Chemical Properties

• CAS DataBase Reference: 1,5,9,13-Tetraazacycloheptadecan-6-one, 8-(4-hydroxyphenyl)-1-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-, (8S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5,9,13-Tetraazacycloheptadecan-6-one, 8-(4-hydroxyphenyl)-1-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-, (8S)-(312908-82-0)
• EPA Substance Registry System: 1,5,9,13-Tetraazacycloheptadecan-6-one, 8-(4-hydroxyphenyl)-1-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-, (8S)-(312908-82-0)

Safety Data

• Hazardous Substances Data: 312908-82-0(Hazardous Substances Data)

Upstream product

• 373360-25-9 (-)-(S)-8-(4-methoxyphenyl)-1,13-bis[(4-methylphenyl)sulfonyl]-1,5,9,13-tetraazacycloheptadecan-6-one 
• 444119-35-1 (-)-(S)-N-(3-aminopropyl)-3-({3-[(4-methylphenylsulfonyl)amino]propyl}amino)-(4-methoxyphenyl)propanamide 
• 360059-20-7 (S)-3-Amino-3-(4-methoxy-phenyl)-propionic acid ethyl ester 
• 321835-85-2 (-)-(S)-3-(4-methoxyphenyl)-N-{3-[(4-methylphenylsulfonyl)amino]propyl}-3-({3-[(4-methylphenylsulfonyl)amino]propyl}amino)propanamide 
• 151813-62-6 (-)-(S)-8-(4-methoxyphenyl)-1,5,9,13-tetraazacycloheptadecan-6-one 
• 943-89-5 (E)-3-(4-methoxyphenyl)acrylic acid 
• 321835-84-1 (-)-(8S)-1-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]-8-(4-methoxyphenyl)-1,5,9,13-tetraazacycloheptadecan-6-one 

Downstream Products

• 114622-14-9 chaenorpine 
• 69721-57-9 (11S,17S,18S)-aphelandrine 
• 71461-13-7 (-)-ephedradine A 

Relevant articles and documents

Biomimetic formation of macrocyclic spermine alkaloids

Dihydroxyverbacine (10), a precursor for oxidative phenol coupling, was obtained via (±)-buchnerine (14), whose synthesis is described. The oxidizing system hemin (ferriprotoporphyrin IX chloride)/H2O2 promoted intramolecular coupling of 10 to give the alkaloids aphelandrine (1), orantine (2), and chaenorpine (7). The alkaloids were identified by on-line coupled HPLC and atmospheric-pressure chemical-ionization (APCI) mass spectrometry.