121511-11-3

Basic information

• Product Name: 3-p-tolylnaphthalen-1-amine
• Synonyms: 3-p-tolylnaphthalen-1-amine
• CAS NO: 121511-11-3
• Molecular Weight: 233.313
• Mol File: 121511-11-3.mol

Chemical Properties

• CAS DataBase Reference: 3-p-tolylnaphthalen-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-p-tolylnaphthalen-1-amine(121511-11-3)
• EPA Substance Registry System: 3-p-tolylnaphthalen-1-amine(121511-11-3)

Safety Data

• Hazardous Substances Data: 121511-11-3(Hazardous Substances Data)

Upstream product

• 1262832-17-6 1-(2-[(4-methylphenyl)ethynyl]phenyl)ethanone 
• 766-97-2 4-n-methylphenylacetylene 
• 38425-35-3 3-p-methylphenyl-1-tetralone 
• 121511-07-7 3-p-Tolyl-3,4-dihydro-2H-naphthalen-1-one oxime 

Relevant articles and documents

Tandem imination/annulation of γ- And δ-ketoalkynes in the presence of ammonia/amines

In this account, we summarize the peculiar effects and advantages of gold, silver, and titanium dual role catalysis over the uncatalyzed tandem imination/annulation processes of γ- and δ-ketoalkynes.

Silver-catalysed intramolecular cyclisation of 2-alkynylacetophenones and 3-acetyl-2-alkynylpyridines in the presence of ammonia

Silver-catalysed/microwave-assisted domino reactions of 2-alkynyl-acetophenones and 3-acetyl-2-alkynylpyridines in the presence of ammonia are widely described. In most cases the reaction give a mixture of the imino- and carbo-cyclisation products, with a

Synthesis of 3-aryl-1-naphthalenamines

1-(Hydroxyimino)-3-aryl-1,2,3,4-tetrahydronaphthalenes, when subjected to Semmler-Wolff reaction using Beckmann's mixture, give hitherto unknown 3-aryl-1-naphthalenamines, which have been characterised using elemental analyses and spectral data.