70301-52-9

Basic information

• Product Name: 2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL
• Synonyms: AKOS AU36-M118;2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL
• CAS NO: 70301-52-9
• Molecular Formula: C₁₂H₁₂N₂O
• Molecular Weight: 200.24
• Mol File: 70301-52-9.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL(70301-52-9)
• EPA Substance Registry System: 2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL(70301-52-9)

Safety Data

• Hazardous Substances Data: 70301-52-9(Hazardous Substances Data)

Usage

General Description

2-(pyridin-2-ylaminomethyl)-phenol is a chemical compound with the molecular formula C12H11N2O. It is a phenolic compound with a pyridine ring and an aminomethyl substituent. 2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL is used in various research and industrial applications, such as in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential antifungal and antioxidant properties. The compound's structure and reactivity make it a versatile building block for the development of new materials and compounds in the field of organic chemistry.

Upstream product

• 1823-47-8 2-(pyridine-2-yliminomethyl)phenol 
• 13563-04-7 N-(2'-pyridyl)-2-hydroxybenzamide 
• 504-29-0 2-aminopyridine 
• 90-02-8 salicylaldehyde 
• 17543-97-4 2-[(1E)-2-aza-2-(2-pyridyl)ethenyl]benzen-1-ol 

Downstream Products

• 949094-00-2 diacetato-bis(N-(2-hydroxybenzyl)-2-aminopyridine)copper(II) 

Relevant articles and documents

Convenient Assembly of Privileged (Hetero)Arene-Fused Benzo[1.4]oxazepines by Two Tandem SNAr Events. Part 2 – The Use of o-[N-(Hetero)aryl]aminomethyl Phenols

As was anticipated based on mechanistic reasoning, bis-nucleophilic o-(arylamino)methyl phenols underwent a facile, base-promoted cyclocondensation with reactivity matched bis-electrophilic (hetero)aromatic substrates to give a rare type of substituted di

A quick route for the synthesis of 3-Aryl-3,4-dihydro-2H-benz[e]-1,3- oxazin-2-ones

N-(2-Hydroxy)-benzyl-arylamines (1) gave substantially pure 3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazin-2-one 2 on cyclization with carbonyldiimidazole in DMSO in 20-30 min at 20-25 °C in excellent yields.

Voltammetric studies of the electrochemical behaviour of salicylidene-2-aminopyridine at a hanging-mercury-drop-electrode

Electrochemical behaviour of salicylidene-2-aminopyridine has been investigated in 0.1M tetraethylammonium perchlorate - dimethylformamide solutions by cyclic voltammetric and convolution potential sweep voltammetric methods.It was found that the depolari