174536-40-4

Basic information

• Product Name: 2-nitro-N-(prop-2'-enyl)benzylamine
• Synonyms: 2-nitro-N-(prop-2'-enyl)benzylamine
• CAS NO: 174536-40-4
• Molecular Weight: 192.217
• Mol File: 174536-40-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-nitro-N-(prop-2'-enyl)benzylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-nitro-N-(prop-2'-enyl)benzylamine(174536-40-4)
• EPA Substance Registry System: 2-nitro-N-(prop-2'-enyl)benzylamine(174536-40-4)

Safety Data

• Hazardous Substances Data: 174536-40-4(Hazardous Substances Data)

Upstream product

• 113561-21-0 C₁₀H₁₀N₂O₂ 
• 552-89-6 2-nitro-benzaldehyde 
• 107-11-9 1-amino-2-propene 
• 612-23-7 2-nitrobenzyl chloride 

Downstream Products

• 495-58-9 1,2,3,3a,4,9-hexahydropyrrolo<2,1-b>quinazoline 
• 1418218-10-6 N-allyl-N-(2-nitrobenzyl)acrylamide 
• 1418218-42-4 1-(2-nitrobenzyl)-1H-pyrrol-2(5H)-one 
• 1383423-82-2 5-(iodomethyl)-3-(2-nitrobenzyl)thiazolidine-2-thione 
• 22499-49-6 2-(prop-2'-enyl)indazole 
• 174536-44-8 2-amino-N-(prop-2'-enyl)benzylamine 

Relevant articles and documents

Synthesis of nitrogen-containing heterocycles via ring-closing ene-ene and ene-yne metathesis reactions: An easy access to 1- and 2-benzazepine scaffolds and five- and six-membered lactams

Novel regioselective ring closing ene-yne metathesis provided an efficient access to different substituted 1-benzazepine scaffolds. The reported synthetic approach could also be used as a powerful tool for the selective formation of a highly functionaliza

The Stereochemistry of Organometallic Compounds. XLII. The Preparation of Quinazolines Involving Rhodium-Catalysed Hydroformylation of 2-Amino-N-alkenylbenzylamines

Rhodium-catalysed reactions of 2-amino-N-alkenylbenzylamines with H2/CO give hexahydropyrrolo- and hexahydropyridoquinazolines.Reactions of N-allyl derivatives give a single regioisomer, and reactions of but-3-enyl analogues give mixtures of pyrrol