1122-43-6

Basic information

• Product Name: 2,6-DIMETHYL-3-HYDROXYPYRIDINE
• Synonyms: 2,6-DIMETHYL-3-HYDROXYPYRIDINE;2,6-DIMETHYL-3-PYRIDINOL;2,6-DIMETHYLPYRIDIN-3-OL;3-HYDROXY-2,6-LUTIDINE;2,6-dimethyl-3-pyridino;2,6-dimethyl-3-oxypyridine;2,6-DIMETHYLPYRIDINE-3-OL;3-Pyridinol, 2,6-diMethyl-
• CAS NO: 1122-43-6
• Molecular Formula: C₇H₉NO
• Molecular Weight: 123.15
• EINECS: 214-348-8
• Mol File: 1122-43-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 210-212°C
• Boiling Point: 278.9 °C at 760 mmHg
• Flash Point: 122.4 °C
• Appearance: /
• Density: 1.083 g/cm³
• Vapor Pressure: 0.00246mmHg at 25°C
• Refractive Index: 1.544
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: DMSO (Slightly, Sonicated), Methanol (Slightly, Sonicated)
• PKA: 10.72±0.10(Predicted)
• CAS DataBase Reference: 2,6-DIMETHYL-3-HYDROXYPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIMETHYL-3-HYDROXYPYRIDINE(1122-43-6)
• EPA Substance Registry System: 2,6-DIMETHYL-3-HYDROXYPYRIDINE(1122-43-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39-37/39
• Hazardous Substances Data: 1122-43-6(Hazardous Substances Data)

Usage

General Description

2,6-DIMETHYL-3-HYDROXYPYRIDINE is an organic compound that belongs to the pyridine family. It is a derivative of pyridine with a hydroxyl group at the 3-position and two methyl groups at the 2 and 6 positions. This chemical is commonly used in the synthesis of pharmaceutical drugs and agrochemicals. It is also used as an intermediate in the production of various organic compounds. 2,6-DIMETHYL-3-HYDROXYPYRIDINE has been studied for its potential biological and pharmacological properties, and it has been found to have antioxidant and neuroprotective effects. However, it is important to handle this chemical with care as it may pose health hazards if not used properly.

InChI:InChI=1/C7H9NO/c1-5-3-4-7(9)6(2)8-5/h3-4,9H,1-2H3

Upstream product

• 3430-33-9 2,6-dimethylpyridin-3-amine 
• 73750-15-9 methyl 5-methyl-2-furyl ketoxime 
• 1121-78-4 5-Hydroxy-2-methylpyridine 
• 77902-90-0 rac-2-(Trifluormethylsulfonyloxy)propionsaeure-ethylester 
• 79-10-7 acrylic acid 
• 75-05-8 acetonitrile 
• 108-48-5 2,6-dimethylpyridine 
• 14187-25-8 3-hydroxy-2,6-bis(hydroxymethyl)pyridine hydrochloride 
• 15513-52-7 3-nitro-2,6-lutidine 
• 42097-42-7 3-hydroxy-2-hydroxymethyl-6-methylpyridine 
• 64270-99-1 1-(5-methylfuran-2-yl)ethan-1-amine 
• 143936-77-0 2,6-bis-bromomethyl-pyridin-3-ol; hydrobromide 
• 98280-34-3 2-chloromethyl-6-methyl-pyridin-3-ol hydrochloride 
• 1193-79-9 2-acetyl-5-methylfuran 

Downstream Products

• 113650-72-9 3-(4,4'-dimethyl-benzhydryloxy)-1,2,6-trimethyl-piperidine 
• 110244-64-9 3-benzhydryloxy-1,2,6-trimethyl-piperidine 
• 923292-01-7 [5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid 2,6-dimethyl-pyridin-3-yl ester 
• 1056461-87-0 3-(2-fluoro-4-nitro-phenoxy)-2,6-dimethyl-pyridine 
• 142896-15-9 methyl 2,6-dimethylpyridine-4-carboxylate 
• 127067-18-9 methyl 2,6-dimethylnicotinate 
• 54221-93-1 2,6-dimethylisonicotinic acid 
• 5860-71-9 2,6-dimethylpyridine-3-carboxylic acid 

Relevant articles and documents

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A new method for preparation of 3-hydroxypyridines from furfurylamines by photooxygenation

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