16519-20-3

Usage

Uses

Used in Fragrance Industry:
[(heptyloxy)methyl]benzene is used as a fragrance ingredient for its sweet, aromatic odor. It is particularly suitable for the production of perfumes and other scented products, adding a pleasant and distinctive scent to these items.
Used in Personal Care Products:
In the personal care industry, [(heptyloxy)methyl]benzene is used as a fragrance component in various products such as lotions, creams, and shampoos. Its sweet, aromatic scent enhances the overall sensory experience of these products, making them more appealing to consumers.
Used in Household Cleaning Products:
[(heptyloxy)methyl]benzene is also utilized in the formulation of household cleaning products, where its pleasant aroma helps to mask unpleasant odors and provide a fresh, clean scent to the environment.
Used as a Precursor in Organic Chemistry:
[(heptyloxy)methyl]benzene serves as an important intermediate in organic chemistry, being used as a precursor in the synthesis of various organic compounds. Its versatile chemical structure allows for further modification and functionalization, making it a valuable building block in the development of new molecules with potential applications in various industries.
Overall, [(heptyloxy)methyl]benzene is a versatile chemical with a wide range of applications in the fragrance, personal care, household cleaning, and organic chemistry industries, primarily due to its sweet, aromatic odor and its utility as a synthetic intermediate.

Upstream product

• 629-04-9 1-Bromoheptane 
• 100-51-6 benzyl alcohol 
• 54314-84-0 1-[(3-bromopropoxy)methyl]-benzene 
• 92273-73-9 n-butylzinc bromide 
• 111-70-6 n-heptan1ol 
• 100-39-0 benzyl bromide 
• 108-88-3 toluene 
• 111-87-5 octanol 
• 100-44-7 benzyl chloride 

Downstream Products

• 620-47-3 1-methyl-3-(phenylmethyl)-benzene 
• 620-83-7 1-methyl-4-(phenylmethyl)benzene 
• 713-36-0 2-benzyltoluene 
• 108-88-3 toluene 
• 111-70-6 n-heptan1ol 
• 65-85-0 benzoic acid 

Relevant academic research and scientific papers

Synthesis of Benzyl Alkyl Ethers by Intermolecular Dehydration of Benzyl Alcohol with Aliphatic Alcohols under the Effect of Copper Containing Catalysts

Synthesis of benzyl alkyl ethers was performed in high yields by intermolecular dehydration of benzyl and primary, secondary, tertiary alcohols under the effect of copper containing catalysts. The formation of benzyl alkyl ethers occurs with participation of benzyl cation.

Vanadium-Catalyzed Oxidative Debenzylation of O-Benzyl Ethers at ppm Level

An advantageous methodology for the oxidative debenzylation of ethers has been developed. Very low amounts of a catalyst system based on vanadyl acetylacetonate and a triazole type pincer ligand allow the selective oxidative cleavage of a number of O-benzyl ethers in the presence of oxygen as the sole oxidant. The methodology tolerates a number of functional groups such as halo-, alkoxy-, or trifluoromethylarenes, alkyne, alkene, ether, and acetal units. Large-scale deprotections can be also carried out by the optimized procedure, which is amenable to enantioenriched reactants as well. (Figure presented.).

Organohalide-catalyzed dehydrative O-alkylation between alcohols: A facile etherification method for aliphatic ether synthesis

Organohalides are found to be effective catalysts for dehydrative O-alkylation reactions between alcohols, providing selective, practical, green, and easily scalable homo- and cross-etherification methods for the preparation of useful symmetrical and unsymmetrical aliphatic ethers from the readily available alcohols. Mechanistic studies revealed that organohalides are regenerated as reactive intermediates and recycled to catalyze the reactions.

Benzylation of arenes with benzyl ethers promoted by the in situ prepared superacid BF3-H2O

An efficient and environmentally friendly benzylation of arenes with benzyl ethers as benzyl donors using BF3-Et2O to generate in situ the superacid BF3-H2O as an efficient promotor has been described. A wide variety of functional groups have been investigated and found to be compatible to give the desired diarylmethanes in yields of up to 99%. The crucial role of the moisture content in this transformation has been demonstrated by detailed investigations. This journal is the Partner Organisations 2014.

A novel method for synthesis of benzyl alkyl ethers using Vanadium-based metal complex catalysts

A novel method has been developed for the synthesis of benzyl alkyl ethers in 25-85% yields via the reaction of toluene with alcohols in a CCl4 medium catalyzed by Et3N-activated VO(acac)2.

Palladium-catalyzed negishi cross-coupling reactions of unactivated alkyl iodides, bromides, chlorides, and tosylates

A single method (2% Pd2(dba)3/8% PCyp 3/NMI in THF/NMP at 80°C; Cyp = cyclopentyl) achieves the cross-coupling of a range of β-hydrogen-containing primary alkyl iodides, bromides, chlorides, and tosylates with an array of alkyl-, alkenyl-, and arylzinc halides. The process is compatible with a variety of functional groups, including esters, amides, imides, nitriles, and heterocycles.

DIRECT SYNTHESES OF ETHERS IN THE PRESENCE OF QUATERNARY AMMONIUM SLATS UNDER MICROWAVE IRRADIATION

Several ethers have been synthesized directly from alcohols and alkyl halides without an additional base, in the presence of a quaternary ammonium salt, under microwave irradiation, within a few minutes.