54221-96-4

Basic information

• Product Name: 6-Methoxypyridine-2-carbaldehyde
• Synonyms: 2-Formyl-6-methoxypyridine ,97%;6-Methoxy-2-pyridinecarbaldehyde;6-Methoxy-2-pyridinecarboxaldehyde,2-Formyl-6-methoxypyridine, 6-Methoxypyridine-2-carbaldehyde;6-Methoxypyridine-2-carboxaldehyde, 96%;2-Formyl-6-methoxypyridine, 6-Methoxypicolinaldehyde;Methoxy-6-pyridinecarboxaldeh;6-Methoxy-2-pyridinecarboxaldehyde 97%;2-FORMYL-6-METHOXYPYRIDINE
• CAS NO: 54221-96-4
• Molecular Formula: C₇H₇NO₂
• Molecular Weight: 137.14
• Product Categories: Heterocycle-Pyridine series
• Mol File: 54221-96-4.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 103-104 ºC (20 MMHG)
• Flash Point: 81 ºC
• Appearance: /
• Density: 1.140
• Vapor Pressure: 0.172mmHg at 25°C
• Refractive Index: 1.532
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 2.44±0.10(Predicted)
• Sensitive: Air Sensitive
• CAS DataBase Reference: 6-Methoxypyridine-2-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Methoxypyridine-2-carbaldehyde(54221-96-4)
• EPA Substance Registry System: 6-Methoxypyridine-2-carbaldehyde(54221-96-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38-43
• Safety Statements: 26-36/37/39
• RIDADR: NA 1993 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 54221-96-4(Hazardous Substances Data)

Usage

Uses

Synthesis of the corresponding α-pyridoin via treatment with NaCN.

InChI:InChI=1/C7H7NO2/c1-10-7-4-2-3-6(5-9)8-7/h2-5H,1H3

Upstream product

• 63071-12-5 (6-methoxy-pyridin-2-yl)-methanol 
• 15226-74-1 dicobalt octacarbonyl 
• 40473-07-2 6-bromo-2-methoxypyridine 
• 17228-64-7 6-chloro-2-methoxypyridine 
• 626-05-1 2,6-Dibromopyridine 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 123506-64-9 6-Methoxy-3-methyl-2-pyridinealdehyde 
• 123506-65-0 6-methoxy-5-methyl-2-pyridinecarboxaldehyde 
• 223446-82-0 (NC₅H₃(OCH₃)CHO)Zn(SC₆F₅)2 
• 1415416-04-4 C₂₅H₂₉NO₄ 
• 1433897-11-0 C₂₂H₂₂N₄O₂ 
• 1618679-78-9 1-(6-methoxy-2-pyridyl)-N-(2-methylsulfanylphenyl)-methanimine 
• 861404-03-7 (E)-N-((6-methoxypyridin-2-yl)methylene)-2,4,6-trimethylbenzenamine 
• 512197-92-1 2-ethynyl-6-methoxypyridine 

Relevant articles and documents

SUBSTITUENT-INCLUDING UREA COMPOUND

An object of the present invention is to provide a compound that has a specific chemical structure having an activation effect on SIRT6 and is useful as an active component for preventing and treating inflammatory diseases. The present invention relates to a compound represented by Formula (1) or a pharmaceutically acceptable salt thereof. (Each symbol in Formula (1) has the same definition as that described in the specification.)

Noncryogenic synthesis of functionalized 2-methoxypyridines by halogen-magnesium exchange using lithium dibutyl(isopropyl)magnesate(1-) and lithium chloride

2-Methoxypyridines functionalized in the 3-, 5-, or 6-position and 2,6-dimethoxypyridines functionalized in the 3-position were prepared from the corresponding bromo or iodo analogues by using lithium dibutyl(isopropyl) magnesate(1-) and lithium chloride

BENZAZEPIN-2(1H)-ONE DERIVATIVES

Compounds of formula (I) and pharmaceutically acceptable salts thereof are agonists at the beta-2 adrenoceptor. They are useful as feed additives for livestock animals.