320423-61-8

Basic information

• Product Name: 2-(4-FLUOROPHENOXY)BENZALDEHYDE
• Synonyms: 4'-Fluoro-2-formyldiphenyl ether
• CAS NO: 320423-61-8
• Molecular Formula: C₁₃H₉FO₂
• Molecular Weight: 216.21
• Product Categories: Aldehydes;C10 to C21;Carbonyl Compounds
• Mol File: 320423-61-8.mol
• Article Data: 6

Chemical Properties

• Melting Point: 53-57 °C
• Boiling Point: 120-122°/0.05mm
• Flash Point: ≥230 °F
• Appearance: /
• Density: 1.229g/cm³
• Vapor Pressure: 0.00118mmHg at 25°C
• Refractive Index: 1.591
• Storage Temp.: 2-8°C
• Sensitive: Air Sensitive
• CAS DataBase Reference: 2-(4-FLUOROPHENOXY)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-FLUOROPHENOXY)BENZALDEHYDE(320423-61-8)
• EPA Substance Registry System: 2-(4-FLUOROPHENOXY)BENZALDEHYDE(320423-61-8)

Safety Data

• Hazard Codes: Xn
• Statements: 22-41
• Safety Statements: 26-39
• WGK Germany: 2
• HazardClass: IRRITANT
• Hazardous Substances Data: 320423-61-8(Hazardous Substances Data)

Usage

General Description

2-(4-Fluorophenoxy)benzaldehyde is a chemical compound with the molecular formula C13H9FO2. It is an organic compound that belongs to the class of benzaldehyde derivatives and contains a fluoro-substituted phenyl ring and a phenoxy group. 2-(4-FLUOROPHENOXY)BENZALDEHYDE is commonly used in the pharmaceutical and agrochemical industries as an intermediate in the synthesis of various biologically active molecules, such as pharmaceutical drugs and herbicides. Its chemical structure and properties make it suitable for use in organic synthesis and drug discovery efforts. Additionally, 2-(4-Fluorophenoxy)benzaldehyde is also utilized in research and development processes for potential drug candidates and related compounds.

InChI:InChI=1/C13H9FO2/c14-11-5-7-12(8-6-11)16-13-4-2-1-3-10(13)9-15/h1-9H

Upstream product

• 732306-64-8 bis(4-fluorophenyl)iodonium triflate 
• 71730-46-6 benzo[e][1,2,3]oxathiazine 2,2-dioxide 
• 1765-93-1 4-fluoroboronic acid 
• 552-89-6 2-nitro-benzaldehyde 
• 859149-01-2 2-(4-fluorophenoxy)-O,N-dimethylbenzamide 
• 371-41-5 4-Fluorophenol 

Downstream Products

• 2839-49-8 2-fluoro-9H-xanthen-9-one 
• 1400883-57-9 C₁₉H₁₅FO₄S 
• 70764-39-5 [2-(4-fluorophenoxy)phenyl]methanol 
• 1393639-33-2 C₁₄H₁₃FN₂OS 
• 1393639-42-3 C₁₅H₁₃FO₃S 
• 866949-75-9 C₁₅H₁₄FNO₂S 
• 859149-02-3 Methyl 2-amino-5-[2-(4-fluorophenoxy)-phenyl]thiazole-4-carboxylate 

Relevant articles and documents

Pyrazinamide compounds, preparation method and application thereof as well as bactericide

The invention relates to the field of pesticide bactericides and discloses pyrazinamide compounds, a preparation method and an application thereof as well as a bactericide. The compounds have the structure shown in formula (I). The pyrazinamide compounds with the novel structure are designed by introducing pyrazine ring fragments in Pyradiflumid and diphenyl ether fragments with wide bioactivity,and the pyrazinamide compounds can be used as novel SDHIs (succinate dehydrogenase inhibitors) or bactericides.

Ligand-free copper-catalyzed O-arylation of nitroarenes with phenols

The first example of ligand-free copper-catalyzed O-arylation of nitroarenes with phenols was developed, achieving unsymmetrical diaryl ethers in moderate to excellent yields. This arylation proceeded smoothly without promotion of the ligands, and displayed great functional group compatibility. Thus, the method represents a new, facile, and cost-effective approach to access unsymmetrical diaryl ethers.

ACYLAMINOTHIAZOLE DERIVATIVES, PREPARATION METHOD THEREOF AND USE OF SAME IN THERAPEUTICS

The invention relates to a compound of formula (I): Wherein R1, R2, R2′, R3, R4 and R5 are as defined herein. The invention also relates to the use of said compound in therapeutics.