1415012-41-7

Basic information

• Product Name: pentafluorophenyl β-{5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carboxamido}-alaninate
• Synonyms: pentafluorophenyl β-{5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carboxamido}-alaninate
• CAS NO: 1415012-41-7
• Molecular Weight: 571.461
• Mol File: 1415012-41-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: pentafluorophenyl β-{5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carboxamido}-alaninate(CAS DataBase Reference)
• NIST Chemistry Reference: pentafluorophenyl β-{5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carboxamido}-alaninate(1415012-41-7)
• EPA Substance Registry System: pentafluorophenyl β-{5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carboxamido}-alaninate(1415012-41-7)

Safety Data

• Hazardous Substances Data: 1415012-41-7(Hazardous Substances Data)

Upstream product

• 1415012-39-3 ethyl β-{5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carboxamido}-alaninate 
• 1415012-38-2 5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carboxylic acid 
• 1415012-37-1 ethyl 5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carbonate 
• 547762-39-0 5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxylic acid 
• 547762-37-8 ethyl 5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxylate 
• 36131-46-1 ethyl 5-nitro-1H-pyrrole-2-carboxylate 
• 53391-41-6 2,2,2-trichloro-1-(5-nitro-1H-pyrrol-2-yl)ethan-1-one 
• 771-61-9 2,3,4,5,6-pentafluorophenol 
• 1415012-40-6 β-{5-{5-{[(tert-butoxy)carbonyl]amino}-1H-pyrrole-2-carboxamido}-1H-pyrrole-2-carboxamido}-alanine 
• 35302-72-8 pyrrol-2-yl trichloromethyl ketone 

Relevant articles and documents

Convenient method for the synthesis of a flexible cyclic polyamide for selective targeting of c-myb G-quadruplex DNA

A convenient efficient method for synthesis of a flexible cyclic polyamide (cβ, 1) was developed through cyclodimerization. Electrospray ionization mass spectrometry and nuclear magnetic resonance results showed that 1 selectively binds to the c-myb G-qua