90035-20-4

Basic information

• Product Name: 4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE
• Synonyms: 4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE
• CAS NO: 90035-20-4
• Molecular Formula: C₁₄H₉F₃O₂
• Molecular Weight: 266.2152696
• Mol File: 90035-20-4.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 326.855°C at 760 mmHg
• Flash Point: 146.524°C
• Appearance: /
• Density: 1.297g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.54
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE(90035-20-4)
• EPA Substance Registry System: 4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE(90035-20-4)

Safety Data

• Hazardous Substances Data: 90035-20-4(Hazardous Substances Data)

Usage

General Description

The chemical 4-(4-trifluoromethyl-phenoxy)-benzaldehyde is a compound with the molecular formula C14H10F3O2. It is a benzaldehyde derivative with a trifluoromethyl group and a phenoxy group attached to the benzene ring. 4-(4-TRIFLUOROMETHYL-PHENOXY)-BENZALDEHYDE is commonly used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It has also been studied for its potential use in the development of new materials and as a reagent in chemical reactions. Its structural and chemical properties make it an important intermediate in the synthesis of various organic compounds with potential applications in diverse fields.

InChI:InChI=1/C14H9F3O2/c15-14(16,17)11-3-7-13(8-4-11)19-12-5-1-10(9-18)2-6-12/h1-9H

Upstream product

• 402-45-9 4-hydroxybenzotrifluoride 
• 459-57-4 4-fluorobenzaldehyde 
• 555-16-8 4-nitrobenzaldehdye 
• 128796-39-4 4-trifluoromethylphenylboronic acid 

Downstream Products

• 39634-42-9 p-[4-(trifluoromethyl)phenoxy]phenol 
• 117114-01-9 4-(4'-trifluoromethylphenoxy)-benzyl bromide 
• 1201663-83-3 N-(4-fluorobenzyl)-1-(4-(4-(trifluoromethyl)phenoxy)phenyl)methanamine 
• 179056-34-9 cycloheptyl-[4-(4-trifluoromethyl-phenoxy)-benzyl]-amine 
• 656235-20-0 2-imino-5-(4-{3-[2-propyl-4-(4-trifluoromethyl-phenoxy)-phenoxy]-propoxy}-phenyl)-thiazolidin-4-one 
• 592508-49-1 hydroxy-(4-{3-[2-propyl-4-(4-trifluoromethyl-phenoxy)-phenoxy]-propoxy}-phenyl)-acetic acid methyl ester 
• 209809-35-8 4-(4-trifluoromethylphenoxy)-2-propylphenol 
• 592508-74-2 C₁₆H₁₃F₃O₂ 

Relevant articles and documents

Pyrimidine onium compound and application thereof

The invention relates to a pyrimidine onium compound, nitride oxides, salt of the nitride oxides and a composition comprising the compound. The invention further relates to an application of the compound to plant pest control.

Compounds

Pyrimidone compounds of formula (I): are inhibitors of the enzyme Lp-PLA2 and are of use in treating atherosclerosis.

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.