15889-32-4

Basic information

• Product Name: 2-(3-AMINOPHENYL)PYRIDINE
• Synonyms: 2-(3-AMINOPHENYL)PYRIDINE;3-(Pyridin-2-yl)aniline;p60068;3-Pyridin-2-yl-phenylaMine;2-(m-Aminophenyl)pyridine;3-(2-Pyridinyl)aniline;3-(2-Pyridinyl)benzenamine
• CAS NO: 15889-32-4
• Molecular Formula: C₁₁H₁₀N₂
• Molecular Weight: 170.21
• Product Categories: Amines and Anilines;Heterocycles;Amines;Phenyls & Phenyl-Het;Phenyls & Phenyl-Het;Heterocycle-Pyridine series
• Mol File: 15889-32-4.mol
• Article Data: 27

Chemical Properties

• Melting Point: 72-73℃
• Boiling Point: 357.549 °C at 760 mmHg
• Flash Point: 197.323 °C
• Appearance: /
• Density: 1.133 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.626
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 4.81±0.12(Predicted)
• CAS DataBase Reference: 2-(3-AMINOPHENYL)PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-AMINOPHENYL)PYRIDINE(15889-32-4)
• EPA Substance Registry System: 2-(3-AMINOPHENYL)PYRIDINE(15889-32-4)

Safety Data

• Hazard Codes: T
• Statements: 25-36/37/38
• Safety Statements: 26-45
• Hazardous Substances Data: 15889-32-4(Hazardous Substances Data)

Usage

General Description

2-(3-Aminophenyl)pyridine is a chemical compound with the molecular formula C11H10N2. It is a derivative of pyridine and contains a pyridine ring attached to a phenyl ring with an amino group at the 3-position of the phenyl ring. 2-(3-AMINOPHENYL)PYRIDINE has potential applications in organic synthesis, pharmaceuticals, and materials science. It is commonly used as a building block in the synthesis of various organic compounds and as a ligand in coordination chemistry. Additionally, it has been studied for its potential pharmacological properties, including its potential as an anti-cancer agent.

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

Upstream product

• 109-04-6 2-bromo-pyridine 
• 30418-59-8 3-Aminophenylboronic acid 
• 626-01-7 3-Iodoaniline 
• 1008-89-5 2-phenylpyridine 
• 17997-47-6 2-tri-n-butylstannylpyridine 
• 591-19-5 m-Bromoaniline 
• 99-03-6 1-(3-aminophenyl)ethanone 
• 109-76-2 Trimethylenediamine 
• 85006-23-1 3-aminophenylboronic acid hydrochloric salt 
• 109-09-1 2-chloropyridine 
• 13331-27-6 m-nitrobenzene boronic acid 
• 645-00-1 m-iodonitrobenzene 
• 142-08-5 2-hydroxypyridin 
• 4253-79-6 2-(3-nitrophenyl)pyridine 

Downstream Products

• 1056016-04-6 2-chloro-6-[3-(2-pyridyl)phenylamino]-9-iso-propylpurine 
• 1056016-06-8 DRF 053 
• 879085-55-9 vismodegib 
• 1432666-69-7 C₂₂H₁₇N₃ 
• 1546890-05-4 C₃₄H₂₅N₃ 
• 1546890-15-6 C₂₈H₂₁N₃ 
• 1415022-43-3 C₁₃H₁₀Cl₂N₂O 

Relevant articles and documents

Characteristics of polymer light emitting diode using a phosphorescent terpolymer containing perylene, triazine and ir(ppy)3 moieties in the polymer side chain

We have synthesized a novel nonconjugated phosphorescent terpolymer, PPPMA-co-DTPM-co-Ir(ppy)3, containing perylene and Ir complex moieties as lightemitting units and a triazine moiety as electron transporting unit in the polymer side chain. Th

The two isomers of a cyclometallated palladium sensitizer show different photodynamic properties in cancer cells

This report demonstrates that changing the position of the carbon-metal bond in a polypyridyl cyclopalladated complex, i.e. going from PdL1 (N^N^C^N) to PdL2 (N^N^N^C), dramatically influences the photodynamic properties of the compl

Preparation methods of Vismodegib and intermediate of Vismodegib

The invention provides preparation methods of Vismodegib and an intermediate of the Vismodegib, namely, preparation methods of 2-chloro-N-(4-chloro-3-(2-pyridinyl)phenyl)-4-(methylsulfonyl)benzamide and an intermediate of the 2-chloro-N-(4-chloro-3-(2-pyridinyl)phenyl)-4-(methylsulfonyl)benzamide. According to the preparation methods, the intermediate, namely 2-chloro-4-methylsulfonyl-N-(3-(2-pyridinyl)phenyl)benzamide is prepared firstly, and then the 2-chloro-N-(4-chloro-3-(2-pyridinyl)phenyl)-4-(methylsulfonyl)benzamide is prepared through a chlorination reaction. The preparation methods have the characteristics that the steps are short, operation is easy, starting materials are cheap and easy to obtain, no palladium reagent is used, the reaction condition has the low requirements for the anhydrous and oxygen-free condition, and the production cost can be effectively lowered.

Organic metal compounds and organic light emitting diodes comprising the same

PURPOSE: An organic metal compound is provided to have excellent thermal properties and light emitting efficiency, thereby being useful for a display and lighting device. CONSTITUTION: An organic metal compound is represented by chemical formula 1. In chemical formula 1, each of R and Z is hydrogen, deuterium, cyano, halogen hydroxy, nitro, C1-40 alkyl, C1-40 alkoxy, C1-40 alkylamino, C6-40 arylamino, C3-40 heteroarylamino, C1-40 alkoxy group, C1-40 alkylamino, C6-40 aryl group, C3-40 aryloxy group, germanium, phosphorous, and boron; each of A, B, C, D, and E is a substituted or unsubstituted aromatic cycle, or substituted or unsubstituted hydrocycle, X is carbon or nitrogen, G is chemical bond or C1-4 alkylene which can be substituted by (R-Zi)n.