1611447-14-3

Basic information

• Product Name: C₁₉H₂₄N₄O₅
• Synonyms: C₁₉H₂₄N₄O₅
• CAS NO: 1611447-14-3
• Molecular Weight: 388.423
• Mol File: 1611447-14-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₉H₂₄N₄O₅(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₉H₂₄N₄O₅(1611447-14-3)
• EPA Substance Registry System: C₁₉H₂₄N₄O₅(1611447-14-3)

Safety Data

• Hazardous Substances Data: 1611447-14-3(Hazardous Substances Data)

Upstream product

• 583-68-6 2-bromo-p-toluidine 
• 948592-80-1 4‐methyl‐2‐(4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolan‐2‐yl)aniline 
• 188528-95-2 1-(tert-butyl) 3-ethyl 2-oxopyrrolidine-1,3-dicarboxylate 
• 1579291-76-1 2-azido-5-methylphenylboronic acid pinacolate ester 

Relevant articles and documents

Efficient synthesis of 3 H-indoles enabled by the lead-mediated α-arylation of β-ketoesters or γ-lactams using aryl azides

The development of a lead-mediated α-arylation reaction between aryl azides and β-ketoesters or γ-lactams that facilitates the formation of 3H-indoles is disclosed. Twenty-five examples are included which demonstrate the generality of this reaction to access aryl azides bearing tetrasubstituted o-alkyl substituents. When paired with a Staudinger reduction, this reaction streamlines the synthesis of functionalized 3H-indoles.