156094-63-2

Basic information

• Product Name: 2-(broMoMethyl)-6-Methoxypyridine
• Synonyms: 2-(broMoMethyl)-6-Methoxypyridine;-6-methoxypyridine
• CAS NO: 156094-63-2
• Molecular Formula: C₇H₈BrNO
• Molecular Weight: 202.04852
• Mol File: 156094-63-2.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-(broMoMethyl)-6-Methoxypyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(broMoMethyl)-6-Methoxypyridine(156094-63-2)
• EPA Substance Registry System: 2-(broMoMethyl)-6-Methoxypyridine(156094-63-2)

Safety Data

• Hazardous Substances Data: 156094-63-2(Hazardous Substances Data)

Usage

General Description

2-(Bromomethyl)-6-methoxypyridine is a chemical compound with the molecular formula C7H8BrNO. It is a derivative of pyridine, a type of heterocyclic compound. This chemical is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in the production of organic chemicals and research applications. The bromomethyl group in the molecule makes it reactive and useful for various chemical reactions, while the methoxy group provides stability and solubility in organic solvents. 2-(broMoMethyl)-6-Methoxypyridine is classified as a hazardous chemical and requires proper handling and storage.

Upstream product

• 63071-03-4 2-methoxy-6-methyl-pyridine 
• 3279-76-3 6-hydroxy-2-methylpyridine 
• 63071-12-5 (6-methoxy-pyridin-2-yl)-methanol 
• 26256-72-4 6-methoxy-pyridine-2-carboxylic acid methyl ester 
• 19621-92-2 6-Hydroxypicolinic acid 
• 26893-73-2 6-methoxypyridine-2-carboxylic acid 
• 54221-96-4 6-methoxypyridine-2-carbaldehyde 

Downstream Products

• 1361225-15-1 ethyl N-(diphenylmethylidene)-3-(6-methoxy-2-pyridinyl)alaninate 
• 1361225-14-0 1,1,1,3,3,3-hexafluoro-2-(4-(2-((6-methoxy-2-pyridinyl)methyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol 
• 1000512-48-0 2‐(6‐methoxypyridin‐2‐yl)acetonitrile 

Relevant articles and documents

Photoisomerization and photoinduced intramolecular hydrogen atom transfer of 2-[2-(2-pyrrolyl)ethenyl]pyridine derivatives

Introduction of an electron-donating methoxy group to 2-[2-(2-pyrrolyl)ethenyl]pyridine, which undergoes photoinduced intramolecular hydrogen atom transfer and one-way trans-to-cis photoisomerization, induced significant changes in these photochemical beh

Azacyclo diketone compound and preparation method thereof

The invention provides an azacyclo diketone compound, which is a compound represented by the following structure defined in the specification, or a pharmaceutically acceptable salt thereof. The invention provides a compound having an inhibitory activity on influenza (flu) virus proliferation, particularly on influenza-related cap-dependent endonuclease to inhibit influenza virus proliferation so as to treat or prevent influenza. The present invention relates to a substituted azacyclo diketone compound having inhibitory activity on cap-dependent endonuclease, and a pharmaceutical composition containing the substituted azacyclo diketone compound.

OX2R COMPOUNDS

Methods and compositions for agonizing a type-2 orexin receptor (OX2R) in a cell determined to be in need thereof, including the general method of (a) administering to a subject a cyclic guanidinyl OX2R agonist and (b) detecting a resultant enhanced wakefulness or increased resistance to diet-induced accumulation of body fat, or abbreviated recovery from general anesthesia or jet lag.