56807-82-0

Basic information

• Product Name: N-(4-methylphenyl)pentamethylenediamine
• Synonyms: N-(4-methylphenyl)pentamethylenediamine
• CAS NO: 56807-82-0
• Molecular Weight: 192.304
• Mol File: 56807-82-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-(4-methylphenyl)pentamethylenediamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methylphenyl)pentamethylenediamine(56807-82-0)
• EPA Substance Registry System: N-(4-methylphenyl)pentamethylenediamine(56807-82-0)

Safety Data

• Hazardous Substances Data: 56807-82-0(Hazardous Substances Data)

Upstream product

• 37699-98-2 4-(4-methylphenylamino)valeronitrile 
• 106-49-0 p-toluidine 
• 6280-87-1 δ-chlorovaleronitrile 
• 110224-25-4 5-chlorovaleric acid p-toluidide 
• 1575-61-7 5-Chlorovaleroyl chloride 
• 1286232-25-4 4-azido-N-(4-methylphenyl)valeramide 

Downstream Products

• 1346528-71-9 1-(4-methylphenyl)-2-ethyl-1,4,5,6,7,8-hexahydro-1,3-diazocine 
• 1293396-98-1 C₁₆H₂₄N₂ 
• 1346528-60-6 N-propionyl-N'-(4-methylphenyl)-1,5-diaminopentane 
• 1360871-89-1 N-(4-chlorobenzoyl)-N'-(4-methylphenyl)pentamethylenediamine 
• 905456-42-0 C₁₉H₂₂N₂ 
• 1360871-78-8 C₂₀H₂₄ClN₂⁽¹⁺⁾*I^(1-) 
• 1360871-77-7 C₂₀H₂₅N₂⁽¹⁺⁾*I^(1-) 
• 1360871-85-7 2-(4-chlorophenyl)-1-(4-methylphenyl)-1,4,5,6,7,8-hexahydro-1,3-diazocine 
• 1293397-00-8 N-isobutyryl-N'-(4-methylphenyl)-1,5-diaminopentane 

Relevant articles and documents

An Efficient Synthesis of N-Alkyl-N-arylputrescines and Cadaverines

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1,n-Diamines. Part 4: Synthesis of 1-aryl-2-alkyl-1,4,5,6,7,8-hexahydro-1, 3-diazocines

In this Letter we present the synthesis of hitherto unreported 1-aryl-2-alkyl-1,4,5,6,7,8-hexahydro-1,3-diazocines 1. Cyclic amidines 1 were synthesized by PPSE promoted ring closure of N-acyl-N'-arylpen- tamethylenediamines 2. The cyclodehydration reacti

New synthetic route for selectively substituted 1,n-diamines. Synthesis of N-aryl tetra- and pentamethylenediamines

A general procedure for the synthesis of N-aryltetra- and pentamethylenediamines 1 by acid hydrolysis of N-aryl-N'-acylalkylenediamines 2 under microwave irradiation is described. The precursors 2 are obtained by amination of the corresponding N-(x-haloal