194017-69-1

Basic information

• Product Name: 4-(PYRID-2-YLOXY)BENZALDEHYDE
• Synonyms: 4-(PYRID-2-YLOXY)BENZALDEHYDE;4-(Pyridin-2-yloxy)benzaldehyde;4-(Pyridin-2-yloxy)benzaldehyde 97%;4-(2-Pyridyloxy)benzaldehyde;4-(2-Pyridinyloxy)-benzaldehyde;2-(4-Formylphenoxy)pyridine;4-[(Pyridin-2-yl)oxy]benzaldehyde 97+%
• CAS NO: 194017-69-1
• Molecular Formula: C₁₂H₉NO₂
• Molecular Weight: 199.21
• Mol File: 194017-69-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 45 °C
• Boiling Point: 344.8°Cat760mmHg
• Flash Point: 162.3°C
• Appearance: /
• Density: 1.207g/cm³
• Vapor Pressure: 6.41E-05mmHg at 25°C
• Refractive Index: 1.614
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-(PYRID-2-YLOXY)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(PYRID-2-YLOXY)BENZALDEHYDE(194017-69-1)
• EPA Substance Registry System: 4-(PYRID-2-YLOXY)BENZALDEHYDE(194017-69-1)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 194017-69-1(Hazardous Substances Data)

Usage

General Description

4-(pyrid-2-yloxy)benzaldehyde is a chemical compound with the molecular formula C12H9NO2. It is a benzaldehyde derivative with a pyridyl ether functional group attached to the aromatic ring. 4-(PYRID-2-YLOXY)BENZALDEHYDE is commonly used in organic synthesis and chemical research as a building block for the preparation of various intermediates and target molecules. It has been studied for its potential applications in the pharmaceutical and agrochemical industries. The compound exhibits aromatic and aldehyde moieties which are valuable in chemical reactions and can be utilized in the development of new materials and bioactive compounds.

InChI:InChI=1/C12H9NO2/c14-9-10-4-6-11(7-5-10)15-12-3-1-2-8-13-12/h1-9H

Upstream product

• 109-09-1 2-chloropyridine 
• 123-08-0 4-hydroxy-benzaldehyde 
• 372-48-5 2-fluoropyridine 
• 17455-13-9 18-crown-6 ether 
• 109-04-6 2-bromo-pyridine 

Downstream Products

• 194017-70-4 2-(4-Hydroxymethylphenoxy)pyridine 
• 726127-36-2 {1-[(4-(2-pyridyloxy)phenyl)methyl](4-piperidyl)}[4-(trifluoromethyl)phenyl]methan-1-ol 
• 1177252-08-2 1-{(1-benzyl-1H-tetrazol-5-yl)[4-(pyridin-2-yloxy)phenyl]methyl}-4-cyclobutyl-1,4-diazepane 
• 2420-16-8 4-hydroxy-3-chlorobenzaldehyde 

Relevant articles and documents

Synthesis, evaluation, molecular docking, and molecular dynamics studies of novel N-(4-[pyridin-2-yloxy]benzyl)arylamine derivatives as potential antitubercular agents

A new series of novel triclosan (2,4,4′-trichloro-2′-hydroxydiphenylether) analogues were designed, synthesized, and screened for their in vitro antimycobacterial and antibacterial activities. Most of the compounds showed significant activity against Myco

Highly efficient copper-catalyzed O-arylation using readily available (S)-N-methylpyrrolidine-2-carboxamide as the ligand

A highly efficient and readily available catalyst system for O-arylation of various phenols using CuI and (S)-N-methylpyrrolidine-2-carboxamide (Pro-NHMe) was developed. The reaction is widely applicable to the synthesis of diaryl ethers. Georg Thieme Verlag Stuttgart.

Substituted aromatic ethers as inhibitors of glycine transport

This invention relates to a series of substituted aromatic ethers of the formula I wherein ring A and X and Y are defined as in the specification, that exhibit activity as glycine transport inhibitors, their pharmaceutically acceptable salts, pharmaceutic