67565-47-3

Usage

Appearance

Yellow crystalline substance A solid with a yellow color and a crystalline structure.

Molecular weight

259.27 g/mol The mass of one mole of the compound, which is 259.27 grams.

Usage in organic synthesis

Building block for various pharmaceuticals and biologically active compounds It serves as a starting material or intermediate in the synthesis of different organic compounds, including drugs and other biologically relevant molecules.

Usage in agrochemicals and dyes

Reagent in production It is used as a chemical reagent in the manufacturing process of agricultural chemicals and dyes.

Usage in fragrance and flavor compounds

Manufacturing The compound is involved in the production of fragrances and flavor compounds for various applications.

Potential toxicity and health hazards

Handle with care and proper safety procedures Due to possible harmful effects, it is important to follow safety guidelines and precautions when working with 1-methyl-4-[(4-nitrobenzyl)oxy]benzene.

Upstream product

• 106-44-5 p-cresol 
• 100-14-1 4-nitrobenzyl chloride 
• 1192-96-7 potassium p-cresolate 
• 100-11-8 1-bromomethyl-4-nitro-benzene 

Downstream Products

• 68223-16-5 4-methylphenyl 4-aminobenzyl ether 
• 106-44-5 p-cresol 
• 106-49-0 p-toluidine 

Relevant academic research and scientific papers

Cesium fluoride-Celite: A solid base for efficient syntheses of aromatic esters and ethers

Coupling reactions of a number of aromatic and heteroaromatic phenols with alkyl, acyl or benzoyl halides in acetonitrile with cesium fluoride-Celite are described, demonstrating that this reagent provides an efficient, convenient and practical method for the syntheses of aromatic esters and ethers.

Synthesis of aromatic ethers without organic solvent and inorganic carrier under microwave irradiation

A simple, rapid and efficient procedure for the synthesis of aromatic ethers via microwave irradiation without any organic solvent and inorganic carrier is reported.

Electron Apportionment in Cleavage of Radical Anions. 1. Nitro-Substituted Benzyl Phenyl Ethers

The radical anions of 4-nitrobenzyl phenyl ethers undergo cleavage at least 10E4 times faster than the radical anions of corresponding 4-nitrophenyl benzyl ethers despite a perceived thermodynamic advantage for the latter set of reactions.It is suggested that this results reflects a kinetic advantage for cleavage reactions which take place with regioconservation of spin density.