50501-31-0

Basic information

• Product Name: 6-(AMINOMETHYL)-2-PYRIDINEMETHANOL
• Synonyms: 6-(AMINOMETHYL)-2-PYRIDINEMETHANOL;6-HYDROXYMETHYL-PYRIDINE-2-METHANAMINE;2-(Aminomethyl)-6-(hydroxymethyl)pyridine;[6-(Aminomethyl)pyridin-2-yl]methanol
• CAS NO: 50501-31-0
• Molecular Formula: C₇H₁₀N₂O
• Molecular Weight: 138.17
• Mol File: 50501-31-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 276.4 °C at 760 mmHg
• Flash Point: 120.9 °C
• Appearance: /
• Density: 1.186 g/cm³
• Vapor Pressure: 0.00232mmHg at 25°C
• Refractive Index: 1.588
• Storage Temp.: 2-8°C(protect from light)
• PKA: 13.30±0.10(Predicted)
• CAS DataBase Reference: 6-(AMINOMETHYL)-2-PYRIDINEMETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(AMINOMETHYL)-2-PYRIDINEMETHANOL(50501-31-0)
• EPA Substance Registry System: 6-(AMINOMETHYL)-2-PYRIDINEMETHANOL(50501-31-0)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 50501-31-0(Hazardous Substances Data)

Usage

General Description

6-(Aminomethyl)-2-pyridinemethanol is a chemical compound that contains a pyridine ring with a hydroxyl group and an amino-methyl side chain. It has a molecular formula of C7H10N2O and a molecular weight of 138.17 g/mol. 6-(Aminomethyl)-2-pyridinemethanol is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It also has potential applications in the field of organic chemistry as a versatile intermediate for the preparation of various functionalized compounds. Additionally, 6-(Aminomethyl)-2-pyridinemethanol may have biological activities and pharmacological properties that make it a subject of interest in medicinal chemistry research.

InChI:InChI=1/C7H10N2O/c8-4-6-2-1-3-7(5-10)9-6/h1-3,10H,4-5,8H2

Upstream product

• 1122-71-0 2-(Hydroxymethyl)-6-methylpyridine 
• 1190947-26-2 2-[(6-methyl-2-pyridyl)methyl]isoindoline-1,3-dione 
• 40054-01-1 (6-(bromomethyl)pyridin-2-yl)methanol 
• 1195-59-1 2.6-bis(hydroxymethyl)pyridine 
• 154696-52-3 2-[(6-hydroxymethyl-2-pyridyl)methyl]isoindoline-1,3-dione 

Downstream Products

• 153621-48-8 tert-butyl N-[(6-hydroxymethyl-2-pyridyl)methyl]carbamate 
• 1065080-07-0 6-(3-chloro-4-fluorobenzyl)-N-{[6-(hydroxymethyl)pyridin-2-yl]methyl}pyrazolo[1,5-a]pyrimidine-3-carboxamide 

Relevant articles and documents

NOVEL LINEAR ALPHA-OLEFIN CATALYSTS AND PREPARATION AND USE THEREOF

The present invention relates to a novel linear a-olefin catalyst composition, and preparation and use thereof. The catalyst composition includes a main catalyst and a co-catalyst, wherein the main catalyst is an imino-based iron coordination compound, and the co-catalyst is a mixture of methylaluminoxane, triisobutylaluminum, and borane or GaCl3. The catalyst composition can be used to catalyze ethylene oligomerization to produce linear α-olefins having a selectivity of greater than 96%, carbon distribution between C4-C28 with the component of C6-C20 being greater than 75%. The catalyst of the invention is stable in structure and can be used for ethylene oligomerization with high catalytic efficiency. The method of the invention has the advantages of relatively convenient in operation, readily available of raw materials, high yield, low costs, less pollution and easy for industrial production.

Convenient and Multistep Preparation of Oligopyridines Bearing Multiple Dansyl and Nitroxide Radicals

A series of pyridine and bipyridine molecules combining dual fluorescent (dansyl) and magnetic (free radical) probes has been prepared by a linear multistep protocol from the corresponding monodansylated derivatives. The grafting of the flexible aliphatic radical is realized by the use of a chloromethylnitronyl nitroxide derivative under basic conditions and with KI as a mediator. The synthetic potential of 2-[(5-dimethylamino-1-naphthalenesulfonamide)methyl]-6-formylpyridine is assessed by the construction, in a first step, of an aliphatic nitroxide radical and subsequently of an additional aromatic radical. The synthetic methods reported herein provide a practical approach to the rational design of ligands bearing various kinds of functionalities such as chromogenic and spinlabeled fragments. A significant merit of this method is that it allows the introduction of the fluorescent substituent onto the pyridine or bipyridine framework at the beginning of the synthetic protocol.