6631-37-4

Basic information

• Product Name: 2-ANILINOPYRIDINE
• Synonyms: AURORA KA-6558;2-PHENYLAMINOPYRIDINE;2-ANILINOPYRIDINE;N-2-pyridylaniline;phenyl-2-pyridiylamine;N-(2-Pyridinyl)aniline;N-Phenylpyridine-2-amine;Phenyl(2-pyridinyl)amine
• CAS NO: 6631-37-4
• Molecular Formula: C₁₁H₁₀N₂
• Molecular Weight: 170.21
• EINECS: 229-625-9
• Mol File: 6631-37-4.mol
• Article Data: 132

Chemical Properties

• Melting Point: 106-112℃
• Boiling Point: 205-206℃/7mm
• Flash Point: 136.9 °C
• Appearance: /Solid
• Density: 1.249
• Vapor Pressure: 0.000966mmHg at 25°C
• Refractive Index: 1.642
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 5.58±0.10(Predicted)
• CAS DataBase Reference: 2-ANILINOPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ANILINOPYRIDINE(6631-37-4)
• EPA Substance Registry System: 2-ANILINOPYRIDINE(6631-37-4)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 6631-37-4(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 91, p. 5672, 1969 DOI: 10.1021/ja01048a059

InChI:InChI=1/C11H10N2/c1-2-6-10(7-3-1)13-11-8-4-5-9-12-11/h1-9H,(H,12,13)

Upstream product

• 504-29-0 2-aminopyridine 
• 108-86-1 bromobenzene 
• 591-50-4 iodobenzene 
• 109-09-1 2-chloropyridine 
• 150-13-0 4-amino-benzoic acid 
• 118-92-3 anthranilic acid 
• 62-53-3 aniline 
• 109-04-6 2-bromo-pyridine 
• 16344-24-4 2-(phenylamino)nicotinic acid 
• 694-59-7 pyridine N-oxide 
• 103-71-9 phenyl isocyanate 
• 84021-13-6 N-tosyl-N-phenyl-2-aminopyridine 
• 107735-32-0 2-aminopyridine 
• 74642-02-7 3-Phenyl-3a,7a-dihydro-3H-oxazolo[4,5-b]pyridin-2-one 

Downstream Products

• 6631-38-5 nitroso-phenyl-[2]pyridyl-amine 
• 261-96-1 1-azaphenothiazine 
• 130468-99-4 2C₁₁H₉N₂^(1-)*3C₆H₁₈N₃OP*2Na⁽¹⁺⁾ 
• 33287-58-0 C₁₇H₁₆N₂O₂ 
• 61656-89-1 2-(N-ethoxycarbonyl-N-phenyl)aminopyridine 
• 107735-38-6 N-phenyl-N-(2-pyridinyl)-N'-(4-nitrophenyl)urea 
• 107735-36-4 N,N'-diphenyl-N-(2-pyridinyl)urea 
• 107735-37-5 N-phenyl-N-(2-pyridinyl)-N'-(4-methylphenyl)urea 
• 107735-32-0 2-aminopyridine 
• 124068-66-2 4-(chloromethyl)-2-oxo-1-phenylpyrido<1,2-a>pyrimidin-5-ium-3-olate 

Relevant articles and documents

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND A ELECTRONIC DEVICE THEREOF

In the present invention, provided is a novel compound capable of improving luminance efficiency, stability, and service life of an element, an organic electronic element using the same, and an electronic device thereof. By using the compound of the present invention, high luminance efficiency, low driving voltages, and high heat resistance of the element can be achieved, and color purity and service life of the element can be greatly improved.

ORGANIC ELECTROLUMINESCENCE DEVICE AND ORGANOMETALLIC COMPLEX FOR ORGANIC ELECTROLUMINESCENCE DEVICE

Provided is an organic electroluminescence device. The organic electroluminescence device according to an embodiment includes a first electrode, a second electrode facing the first electrode, and a plurality of organic layers between the first electrode and the second electrode, wherein at least one of the plurality of organic layers includes an organometallic complex including a metal atom which is a central atom, a plurality of ligand connected to the metal atom, and a nitrogen atom connecting two of the plurality of ligands. The nitrogen atom includes an aromatic ring group as a substituent. The aromatic ring group is not bonded to any of the plurality of ligands to form a ring, thereby allowing the organic electroluminescent device to exhibit a low drive voltage and improved life time.

Nickel-Catalyzed Amination of Aryl Nitriles for Accessing Diarylamines through C?CN Bond Activation

A nickel-catalyzed amination to access diarylamines has been developed through C?CN bond activation of aryl nitriles with anilines. In this developed catalytic protocol, various aromatic and heteroaromatic nitriles could be utilized as the electrophiles to couple with substituted anilines. A diversity of diarylamines were obtained in 15–95% yields. (Figure presented.).