22950-23-8

Basic information

• Product Name: N-(prop-2-en-1-yl)naphthalen-1-amine
• CAS NO: 22950-23-8
• Molecular Formula: C₁₃H₁₃N
• Molecular Weight: 183.249
• Mol File: 22950-23-8.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 323°C at 760 mmHg
• Flash Point: 158.3°C
• Density: 1.07g/cm³
• Vapor Pressure: 0.00027mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: N-(prop-2-en-1-yl)naphthalen-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(prop-2-en-1-yl)naphthalen-1-amine(22950-23-8)
• EPA Substance Registry System: N-(prop-2-en-1-yl)naphthalen-1-amine(22950-23-8)

Safety Data

• Hazardous Substances Data: 22950-23-8(Hazardous Substances Data)

Usage

General Description

N-(prop-2-en-1-yl)naphthalen-1-amine is a chemical compound with the molecular formula C12H11N. It is an organic amine, also known as 1-(2-propenyl)naphthalene, and is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. N-(prop-2-en-1-yl)naphthalen-1-amine is characterized by a naphthalene ring with an attached propenyl group and an amine functional group. It has been studied for its potential applications in the field of medicinal chemistry and organic synthesis due to its unique structure and reactivity. Additionally, it may also have uses in the production of dyes and other organic compounds.

Upstream product

• 591-87-7 Allyl acetate 
• 134-32-7 1-amino-naphthalene 
• 107-05-1 3-chloroprop-1-ene 
• 78977-64-7 N-allyl-N-trifluoroacetyl-1-naphthylamine 
• 7575-57-7 allyl benzenesulfonate 
• 106-95-6 allyl bromide 
• 837-78-5 N-trifluoroacetyl-α-naphthylamine 
• 35466-83-2 allyl methyl carbonate 
• 107-18-6 allyl alcohol 

Downstream Products

• 1599475-53-2 C₂₂H₂₁IN₂S 
• 1599475-52-1 C₂₁H₁₉IN₂OS 
• 1599475-51-0 C₂₀H₁₆FIN₂S 
• 1599475-50-9 C₂₀H₁₆ClIN₂S 
• 1599475-49-6 C₂₀H₁₇IN₂S 
• 1316312-15-8 N-(2-buta-1,3-dienyl-naphthalen-1-yl)-4-methyl-benzenesulfonamide 
• 1226515-82-7 1-tosyl-2,5-dihydro-1H-naphtho[1,2-b]azepine 
• 1226515-69-0 N,2-diallyl-N-tosyl-1-naphthylamine 
• 78977-71-6 2-(2-propenyl)-1-naphthylamine 
• 134-32-7 1-amino-naphthalene 
• 863656-29-5 2-(2-propenyl)-1-(triphenylphosphoranylideneamino)naphthalene 
• 863656-31-9 13-phenyl-7,7a,8,14-tetrahydrodibenzo[b,h]acridine 
• 607-60-3 N-propylnaphthalen-1-amine 

Relevant articles and documents

Direct palladium(0)-catalyzed amination of allylic alcohols with aminonaphthalenes

The direct activation of C-O bonds in allylic alcohols by palladium complexes has been accelerated by carrying out the reactions in the presence of titanium reagents. The palladium-catalyzed amination of allylic alcohols using aminonaphthalenes gave N-all

PEG-4000-promoted palladium-catalyzed N-allylation in water: Aminonaphthalene as an example

An environmentally friendly, efficient catalytic process using palladium associated with ligands in a PEG4000-water system leading to N-allylation was described in this study. PEG-4000 was found to improve the palladium-catalyzed allylic amination of allylic acetates with aminonaphthalenes and gave overall good to high yields of the corresponding N-allylic aminonaphthalenes. Copyright

Synthesis of azepine- and azocine-annulated heterocycles by aromatic aza-Claisen rearrangement and ring-closing metathesis

Syntheses of hitherto unreported azepine- and azocine-annulated heterocycles have been developed in excellent yields via a catalyzed aromatic aza-Claisen rearrangement followed by ring-closing metathesis using Grubbs first-generation catalyst. Georg Thiem