116611-36-0

Basic information

• Product Name: 1-(4-nitro-benzyl)-1H-indole
• Synonyms: 1-(4-nitro-benzyl)-1H-indole
• CAS NO: 116611-36-0
• Molecular Weight: 252.272
• Mol File: 116611-36-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(4-nitro-benzyl)-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-nitro-benzyl)-1H-indole(116611-36-0)
• EPA Substance Registry System: 1-(4-nitro-benzyl)-1H-indole(116611-36-0)

Safety Data

• Hazardous Substances Data: 116611-36-0(Hazardous Substances Data)

Upstream product

• 496-15-1 1-indoline 
• 555-16-8 4-nitrobenzaldehdye 
• 16851-56-2 indolin-2-yl carboxylic acid 

Downstream Products

• 344799-93-5 2-[1-(4-nitrobenzyl)-1H-indol-3-yl]-2-oxo-N-(pyridin-4-yl)acetamide 
• 934706-13-5 1-(4-dibenzylamino-benzyl)-1H-indole-3-carbaldehyde 
• 934706-11-3 dibenzyl-(4-indol-1-ylmethyl-phenyl)-amine 
• 344799-92-4 4-indol-1-ylmethyl-phenylamine 

Relevant articles and documents

Bronsted acid-catalyzed decarboxylative redox amination: Formation of N-alkylindoles from azomethine ylides by isomerization

A Bronsted acid-catalyzed decarboxylative redox amination involving aldehydes with 2-carboxyindoline for the synthesis of N-alkylindoles is described. The decarboxylative condensations of aldehydes with 2-carboxyindoline produce azomethine ylides in situ,

THE REACTION OF SECONDARY α-AMINO ACIDS WITH CARBONYL COMPOUNDS. PROPERTIES OF THE INTERMEDIATE AZOMETHINE YLIDES. OXAZOLIDINE FORMATION VERSUS 1,4-PROTOTROPY.

Cyclic secondary α-amino acids react regiospecifically, via antidipole formation, with aldehydes bearing electron withdrawing substituents to give oxazolidines in good yield.In certain cases structural features in the α-amino acid promote a 1,4-prototropi