955123-34-9

Basic information

• Product Name: 2,2-dimethyl-N-[3-(2-aminophenyl)pyridin-4-yl]propionamide
• Synonyms: 2,2-dimethyl-N-[3-(2-aminophenyl)pyridin-4-yl]propionamide
• CAS NO: 955123-34-9
• Molecular Weight: 269.346
• Mol File: 955123-34-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,2-dimethyl-N-[3-(2-aminophenyl)pyridin-4-yl]propionamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-dimethyl-N-[3-(2-aminophenyl)pyridin-4-yl]propionamide(955123-34-9)
• EPA Substance Registry System: 2,2-dimethyl-N-[3-(2-aminophenyl)pyridin-4-yl]propionamide(955123-34-9)

Safety Data

• Hazardous Substances Data: 955123-34-9(Hazardous Substances Data)

Upstream product

• 70298-89-4 4-N-pivaloylaminopyridine 
• 3302-39-4 1-azido-2-bromobenzene 
• 955123-29-2 C₁₀H₁₅N₂BO₃ 
• 615-36-1 2-bromoaniline 

Downstream Products

• 955123-32-7 2,2-dimethyl-N-[3-(2-azidophenyl)pyridin-4-yl]propionamide 

Relevant articles and documents

First Suzuki-Miyaura type cross-coupling of ortho-azidobromobenzene with arylboronic acids and its application to the synthesis of fused aromatic indole-heterocycles

A short synthesis of some fused indole-heterocycles has been achieved via Pd-catalyzed cross-coupling reactions between azido-2-bromobenzene and arylboronic acids and subsequent thermally induced nitrene insertion. Additionally, 4-amino-α-carboline, a versatile intermediate toward grossularine analogs has also been prepared by Suzuki-Miyaura cross-coupling of 4-pivaloylaminopyridine-3-boronic acid with 2-bromoaniline, followed by simple functional group transformations.