174265-24-8

Basic information

• Product Name: 1-(methoxymethoxy)-4-(trifluoromethyl)benzene
• Synonyms: 1-(methoxymethoxy)-4-(trifluoromethyl)benzene
• CAS NO: 174265-24-8
• Molecular Formula: C₉H₉F₃O₂
• Molecular Weight: 206
• Mol File: 174265-24-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-(methoxymethoxy)-4-(trifluoromethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(methoxymethoxy)-4-(trifluoromethyl)benzene(174265-24-8)
• EPA Substance Registry System: 1-(methoxymethoxy)-4-(trifluoromethyl)benzene(174265-24-8)

Safety Data

• Hazardous Substances Data: 174265-24-8(Hazardous Substances Data)

Usage

General Description

1-(methoxymethoxy)-4-(trifluoromethyl)benzene is a chemical compound with the molecular formula C9H9F3O2. It is a benzene derivative that contains both methoxy and trifluoromethyl functional groups. It is commonly used as a building block in organic synthesis for the production of various pharmaceuticals, agrochemicals, and other fine chemicals. The presence of the methoxy and trifluoromethyl groups in the compound gives it unique chemical properties, making it a valuable intermediate in the synthesis of complex organic molecules. It is important to handle 1-(methoxymethoxy)-4-(trifluoromethyl)benzene with care, as it may be hazardous if not used properly.

Upstream product

• 402-45-9 4-hydroxybenzotrifluoride 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 854472-71-2 2-Methoxymethoxy-5-trifluoromethyl-phenol 
• 1449696-91-6 2-((2-methoxy-5-(trifluoromethyl)phenyl)ethynyl)-4-(trifluoromethyl)phenol 
• 1449696-89-2 2,2′-(ethyne-1,2-diyl)bis[4-(trifluoromethyl)phenol] 
• 1449696-96-1 1,2-bis[2-(methoxymethoxy)-5-(trifluoromethyl)phenyl]ethyne 
• 1449696-95-0 2-ethynyl-1-(methoxymethoxy)-4-(trifluoromethyl)benzene 
• 1449697-07-7 C₂₂H₁₆F₆O₄ 
• 1449697-06-6 1-methoxy-2-((2-(methoxymethoxy)-5-(trifluoromethyl)phenyl)ethynyl)-4-(trifluoromethyl)benzene 
• 1449696-94-9 2-iodo-1-(methoxymethoxy)-4-(trifluoromethyl)benzene 
• 1449696-92-7 2,2′-(buta-1,3-diyne-1,4-diyl)bis(4-(trifluoromethyl)phenol) 
• 79427-88-6 2-hydroxy-5-(trifluoromethyl)benzoic acid 
• 328-90-5 4-trifluoromethylsalicylic acid 

Relevant articles and documents

Siladifluoromethylation and Difluoromethylation onto C(sp3), C(sp2), and C(sp) Centers Using Ruppert-Prakash Reagent and Fluoroform

Siladifluoromethylations and difluoromethylations on sp3, sp2, and sp carbons of lithiated carbamates, arenes, and terminal alkynes, respectively, have been attained by employing the Ruppert-Prakash reagent (CF3TMS) and fl

Discovery and optimization of new chromium catalysts for ethylene oligomerization and polymerization aided by high-throughput screening

High throughput screening (HTS) of a 205 member Schiff base salicylaldimine ligand library derived from salicylaldehydes bearing bulky ortho-substituents, i.e., 9-anthracenyl, 1,4,5,8-tetramethylanthracenyl or triptycenyl, reacted in-situ with (p-tolyl)CrCl2(thf)3, identified two new classes of highly active chromium based systems for the Oligomerization and polymerization of ethylene, respectively. The polymerization system comprises bidentate ortho-substituted anthracenyl Schiff bases bearing small primary or secondary alkyl imine substituents. The Oligomerization catalysts are based upon tridentate orthotriptycenyl-substituted Schiff bases with pyridylmethyl or quinolyl substituents. Validation tests confirmed polymerization productivities of up to 3000 g·mmol-1h-1bar-1 for the polymerization catalyst systems while the oligomerization catalysts gave productivities up to 10 000 g·mmol-1h-1bar -1. Key catalyst precursors have been characterized by X-ray crystallography.