21190-93-2

Basic information

• Product Name: 2-ACETYL-6-METHOXYPYRIDINE 97
• Synonyms: 2-Acetyl-6-Methoxypyridine 97%;2-ACETYL-6-METHOXYPYRIDINE 97;2-Acetyl-6-methoxypyridine;1-(6-Methoxypyridin-2-yl)ethan-1-one;1-(6-Methoxypyridin-2-yl)ethanone
• CAS NO: 21190-93-2
• Molecular Formula: C₈H₉NO₂
• Molecular Weight: 151.164
• Product Categories: Heterocyclic Compounds
• Mol File: 21190-93-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 40-44 °C
• Boiling Point: 85 °C0.2 mm Hg
• Flash Point: 202 °F
• Appearance: /
• Density: 1.093 g/cm³
• Vapor Pressure: 0.159mmHg at 25°C
• Refractive Index: 1.505
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: soluble in Methanol
• PKA: 1.72±0.10(Predicted)
• CAS DataBase Reference: 2-ACETYL-6-METHOXYPYRIDINE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ACETYL-6-METHOXYPYRIDINE 97(21190-93-2)
• EPA Substance Registry System: 2-ACETYL-6-METHOXYPYRIDINE 97(21190-93-2)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26-36/37
• WGK Germany: 3
• Hazardous Substances Data: 21190-93-2(Hazardous Substances Data)

Usage

General Description

2-Acetyl-6-methoxypyridine 97 is a chemical compound with the molecular formula C9H9NO2. It is commonly used in the pharmaceutical and fragrance industries as a building block for the synthesis of various drugs and perfumes. 2-ACETYL-6-METHOXYPYRIDINE 97 is an important component in the creation of flavors and fragrances due to its aromatic properties. It is also used as an intermediate in the production of various pharmaceuticals, including anti-inflammatory and anti-cancer drugs. Additionally, it is known for its potential as an anti-bacterial and anti-microbial agent. Overall, 2-Acetyl-6-methoxypyridine 97 is a versatile chemical that has a wide range of applications in different industries.

InChI:InChI=1/C8H9NO2/c1-6(10)7-4-3-5-8(9-7)11-2/h3-5H,1-2H3

Upstream product

• 40473-07-2 6-bromo-2-methoxypyridine 
• 127-19-5 N,N-dimethyl acetamide 
• 1628-89-3 2-methoxypyridine 
• 75-36-5 acetyl chloride 
• 107465-22-5 C₇H₆LiN₃ 
• 107465-23-6 3-methyl-7-bromo-[1,2,3]triazolo[1,5-a]pyridine 
• 107465-29-2 7-methoxy-3-methyltriazolopyridine 

Downstream Products

• 204569-88-0 2-ethenyl-6-methoxypyridine 
• 137678-86-5 6-Acetyl-2(1H)-pyridone 
• 1426343-78-3 C₂₀H₂₆N₂O 
• 1426343-81-8 C₂₀H₂₆Br₄N₂OSn 
• 1426343-75-0 C₂₀H₂₆ClN₂OSn⁽¹⁺⁾*Cl₃Sn^(1-) 
• 1426343-73-8 C₂₀H₂₆ClGeN₂O⁽¹⁺⁾*Cl₃Ge^(1-) 

Relevant articles and documents

Electrocatalytic Water Oxidation by a Tetranuclear Copper Complex

A novel tetranuclear copper-based water oxidation catalyst was designed and synthesized by using a new multinucleating ligand containing two proton dissociation sites, 1,3-bis(6-hydroxy-2-pyridyl)-1H-pyrazole. The copper complex showed electrocatalytic activity for water oxidation reactions under aqueous basic conditions (pH 12.5) with an overpotential of approximately 500 mV. UV/Vis absorption and energy-dispersive X-ray (EDX) spectroscopic techniques coupled with electrochemical analyses of the catalyst system strongly suggest that the tetranuclear copper complex works as a homogeneous system under the conditions used. The results described here demonstrate the utility of a discrete tetranuclear copper complex in water oxidation reactions.

SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION

Pharmaceutical compositions of the invention are presented which comprise substiuted aminothiazoles derivatives. The substiuted aminothiazoles derivatives have a disease-modifying action in the treatment of diseases associated with unregulated cell growth. Such diseases include cancers such as hepatocellular carcinoma, and viral infections from a hepatitis virus.

TRIAZOLOPYRIDINES. PART 8. NUCLEOPHILIC SUBSTITUTION REACTIONS OF 5-BROMOTRIAZOLOISOQUINOLINE AND 7-BROMO-TRIAZOLOPYRIDINE

Nucleophilic substitution of 5-bromotriazoloisoquinoline (3) and of 7-bromo-3-methyltriazolopyridine (6) proceeds readily to give a range of 5-substituted triazoloisoquinolines (4a)-(4e), and of 7-substituted triazolopyridines (7a)-(7h) respectively.Triazoloisoquinolines have been converted into 1,3-disubstituted isoquinolines (11)-(13), (15), and (16), and triazolopyridines into 2,6-disubstituted pyridines (17)-(19).Of secondary amine nucleophiles, only piperidine reacted with 7-bromo-3-methyl-triazolopyridine (6) to give the 7-substituted derivative (7g).A second product in this reaction was a 2,6-disubstituted pyridine (8); the similar compounds (20)-(24) were the only products when morpholine or N-acetyl-piperazine were used.The reaction between 7-bromotriazolopyridine (9) and piperidine or morpholine gave in high yield the 2,6-disubstituted pyridines (25) and (26).