1137-80-0

Basic information

• Product Name: N,N-Dimethyl-4-(4-pyridinyl)aniline
• Synonyms: 4-[4-(Dimethylamino)phenyl]pyridine;N,N-Dimethyl-4-(4-pyridinyl)aniline;Dimethyl-(4-pyridin-4-yl-phenyl)-amine
• CAS NO: 1137-80-0
• Molecular Formula: C₁₃H₁₄N₂
• Molecular Weight: 198.26
• Mol File: 1137-80-0.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 334°C at 760 mmHg
• Flash Point: 155.8°C
• Appearance: /
• Density: 1.066g/cm³
• Vapor Pressure: 0.000132mmHg at 25°C
• Refractive Index: 1.595
• CAS DataBase Reference: N,N-Dimethyl-4-(4-pyridinyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-Dimethyl-4-(4-pyridinyl)aniline(1137-80-0)
• EPA Substance Registry System: N,N-Dimethyl-4-(4-pyridinyl)aniline(1137-80-0)

Safety Data

• Hazardous Substances Data: 1137-80-0(Hazardous Substances Data)

Usage

General Description

N,N-Dimethyl-4-(4-pyridinyl)aniline is a chemical compound with the molecular formula C13H15N. It is a derivative of aniline and is commonly used in the synthesis of organic compounds. This chemical is often employed in the production of dyes and pigments, as well as in the pharmaceutical industry for the development of certain drugs. It also has applications in the field of materials science, particularly in the manufacturing of polymers and plastics. N,N-Dimethyl-4-(4-pyridinyl)aniline is known for its versatility and is used in a wide range of industrial and commercial processes. However, it is important to handle this compound with care, as it can be toxic if not used properly.

InChI:InChI=1/C13H14N2/c1-15(2)13-5-3-11(4-6-13)12-7-9-14-10-8-12/h3-10H,1-2H3

Upstream product

• 110-86-1 pyridine 
• 121-69-7 N,N-dimethyl-aniline 
• 98-88-4 benzoyl chloride 
• 707-74-4 (trichloromethyl)mesitylene 
• 28611-39-4 4-(dimethylamino)benzene-boronic acid 
• 19524-06-2 4-bromopyridine hydrochloride 
• 5957-96-0 4-(4-chlorophenyl)pyridine 
• 68-12-2 N,N-dimethyl-formamide 
• 637-87-6 1-Chloro-4-iodobenzene 
• 1692-15-5 4-pyridylboronic acid 
• 586-77-6 4-bromo-N,N-dimethylaniline 

Downstream Products

• 91779-24-7 1-(4'-nitrophenyl)-4-(4''-dimethylaminophenyl)pyridinium iodide 
• 175091-14-2 (C₅H₄N)2Re(CO)3(C₅H₄N)(C₆H₄)N(CH₃)2⁽¹⁺⁾ 
• 906061-18-5 (4-(4'-dimethylaminophenyl)pyridine)tungsten pentacarbonyl 

Relevant articles and documents

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The first total synthesis for large-scale production and anticancer activity of novel aminophenylpyridinium-5-(hydroxybenzoyl)hydrazonomethyl-2-oxothiazol-3-ide (PBHT) (1) and its derivatives are reported. The chemical structure of PBHT was unambiguously

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Some reactions of pyridinium salts derived from trichloromethylarenes with N- and C-nucleophiles

The reaction of N-(4-pyridyl)pyridinium and 4-chloropyridinium salts obtained from 1-trichloromethyl-2,4,6-trimethylbenzene and pyridine with N-nucleophiles such as piperidine and morpholine and with C-nucleophiles such as N,N-dimethylaniline and indole proceeds through hetarylation and gives the corresponding 4-substituted pyridines. N-(α,α-Dichlorobenzyl)pyridinium and N,N'-(α-chlorobenzylidene)bispyridinium salts obtained from trichloromethylbenzene do not undergo hetarylation.

Fluorescent substrates for neurotransmitter transporters

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