29528-30-1

Basic information

• Product Name: 2-(2-PYRIDYL)ANILINE
• Synonyms: 2-(2-PYRIDYL)ANILINE;2-PYRIDIN-2-YL-PHENYLAMINE;2-Pyridyl-2-aniline;2-(2-Aminophenyl)pyridine;2-(2-Pyridinyl)aniline;2-(pyridin-2-yl)aniline;2-(2-pyridinyl)Benzenamine
• CAS NO: 29528-30-1
• Molecular Formula: C₁₁H₁₀N₂
• Molecular Weight: 170.21
• Product Categories: pharmacetical
• Mol File: 29528-30-1.mol
• Article Data: 37

Chemical Properties

• Boiling Point: 319.6 °C at 760 mmHg
• Flash Point: 173 °C
• Appearance: /
• Density: 1.133±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.000335mmHg at 25°C
• Refractive Index: 1.625
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-(2-PYRIDYL)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-PYRIDYL)ANILINE(29528-30-1)
• EPA Substance Registry System: 2-(2-PYRIDYL)ANILINE(29528-30-1)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 29528-30-1(Hazardous Substances Data)

Usage

General Description

2-(2-pyridyl)aniline, also known as 2-amino-α-pyridine, is a chemical compound with the molecular formula C11H10N2. It is a pale yellow solid that is primarily used as an intermediate in the production of pharmaceuticals, dyes, and other organic compounds. 2-(2-pyridyl)aniline is also used as a catalyst and as a building block in the creation of various molecules. It is considered to be a hazardous chemical and proper safety precautions should be taken when handling and storing it. Additionally, it has been identified as a potential environmental pollutant and may pose health risks to humans and animals if not properly managed.

InChI:InChI=1/C11H10N2/c12-10-6-2-1-5-9(10)11-7-3-4-8-13-11/h1-8H,12H2

Upstream product

• 109-04-6 2-bromo-pyridine 
• 615-36-1 2-bromoaniline 
• 5570-18-3 2-aminophenylboronic acid 
• 5570-19-4 2-nitrophenylboronic acid 
• 1607824-59-8 2-(2-(pyridin-2-yl)phenyl)benzo[d]isothiazol-3(2H)-one 1,1-dioxide 
• 197958-29-5 pyridin-2-ylboronic acid 
• 109-09-1 2-chloropyridine 
• 191171-55-8 2-anilineboronic acid pinacol ester 
• 76426-76-1 N-[2-(pyridine-2-yl)phenyl]benzamide 
• 615-43-0 2-iodophenylamine 
• 105664-48-0 2-(phenyl-d5)pyridine 
• 1446325-77-4 2-(2-(pyridin-2-yl)phenyl)isoindoline-1,3-dione 
• 1318768-17-0 N-(tert-butyloxycarbonyl)-2-(pyridin-2-yl)aniline 
• 1258862-62-2 2-(2-dibromoborylphenyl)pyridine 

Downstream Products

• 1040922-30-2 2-nitro-N-(2-(pyridin-2-yl)phenyl)benzenesulfonamide 
• 1008-89-5 2-phenylpyridine 
• 1581756-81-1 4-methyl-N-[2-(pyridin-2-yl)phenyl]benzamide 

Relevant articles and documents

Redox-Active Ligand Assisted Catalytic Water Oxidation by a RuIV=O Intermediate

Water splitting is one of the most promising solutions for storing solar energy in a chemical bond. Water oxidation is still the bottleneck step because of its inherent difficulty and the limited understanding of the O?O bond formation mechanism. Molecular catalysts provide a platform for understanding this process in depth and have received wide attention since the first Ru-based catalyst was reported in 1982. RuV=O is considered a key intermediate to initiate the O?O bond formation through either a water nucleophilic attack (WNA) pathway or a bimolecular coupling (I2M) pathway. Herein, we report a Ru-based catalyst that displays water oxidation reactivity with RuIV=(O) with the help of a redox-active ligand at pH 7.0. The results of electrochemical studies and DFT calculations disclose that ligand oxidation could significantly improve the reactivity of RuIV=O toward water oxidation. Under these conditions, sustained water oxidation catalysis occurs at reasonable rates with low overpotential (ca. 183 mV).

Ruthenium-catalyzed: Ortho -selective CAr-H amination of heteroaryl arenes with di- tert -butyldiaziridinone

Application of an oxidative amination reagent (di-tert-butyldiaziridinone) to the Ru3(CO)12-catalyzed ortho-selective CAr-H amination reaction is described. This strategy shows good functional group compatibility with vari

COMPOUNDS AND METHODS FOR TREATING CANCER

Substituted cinnamamide compounds and analogs, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or ameliorate cancer are provided.

Phenanthridine Derivatives and organic light-emitting diode including the same

PURPOSE: A phenanthridine derivative compound is provided to obatin an organic light emitting diode with excellent light emitting property. CONSTITUTION: A phenanthridine derivative compound is denoted by chemical formula 1 or 2. An organic light emitting diode contains an anode, a cathode, and the phenanthridine derivative compounds inserted between the anode and cathode. The organic light emitting diode further contains a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, or an electron injection layer formed by monomer deposition or solution process.