1146732-16-2

Basic information

• Product Name: N-tert-butoxycarbonyl-5-iodo-2-phenyl-1H-pyrrole
• Synonyms: N-tert-butoxycarbonyl-5-iodo-2-phenyl-1H-pyrrole
• CAS NO: 1146732-16-2
• Molecular Weight: 369.202
• Mol File: 1146732-16-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-tert-butoxycarbonyl-5-iodo-2-phenyl-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: N-tert-butoxycarbonyl-5-iodo-2-phenyl-1H-pyrrole(1146732-16-2)
• EPA Substance Registry System: N-tert-butoxycarbonyl-5-iodo-2-phenyl-1H-pyrrole(1146732-16-2)

Safety Data

• Hazardous Substances Data: 1146732-16-2(Hazardous Substances Data)

Upstream product

• 163525-97-1 tert-butyl 2-phenyl-1H-pyrrole-1-carboxylate 

Downstream Products

• 1255323-89-7 C₃₇H₃₈N₂O₄ 
• 1146731-34-1 N-tert-butoxycarbonyl-2-(N-tert-butoxycarbonyl-2-phenyl-1H-pyrrol-5-yl)-1H-indole 

Relevant articles and documents

Synthesis of nonsymmetrical 5-Aryl-2-indolopyrrole derivatives via controlled mono Suzuki-Miyaura cross-coupling on N-Boc-2,5-dibromopyrrole

The first example of mono Suzuki-Miyaura cross-coupling of N-Boc-2,5-dibromopyrrole with a boronic acid (indol-2-ylboronic acid) is reported. The resulting 2-indolyl-5-bromopyrrole derivative was in turn coupled with a variety of aryl- or heteroarylboronic acids thereby providing the corresponding non-symmetrical 2,5-disubstituted pyrroles in good to excellent yields. The tert-butoxycarbonyl (Boc) groups could be easily removed to give the completely deprotected products. Georg Thieme Verlag Stuttgart - New York.