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Usage

Uses

Used in Pharmaceutical Industry:
2-[(4-METHYLBENZYL)OXY]BENZALDEHYDE is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, enhancing their efficacy and properties.
Used in Agrochemical Industry:
In the agrochemical industry, 2-[(4-METHYLBENZYL)OXY]BENZALDEHYDE is utilized as a key component in the production of various agrochemicals. Its chemical properties make it suitable for the creation of effective and targeted pest control solutions.
Used in Fine Chemicals Production:
2-[(4-METHYLBENZYL)OXY]BENZALDEHYDE is also used as a building block in the synthesis of fine chemicals. Its distinct odor and chemical properties contribute to the development of specialty chemicals for various applications, such as fragrances and flavorings.
Handling and Storage:
Due to its potential health hazards, 2-[(4-METHYLBENZYL)OXY]BENZALDEHYDE is typically handled and stored under controlled conditions to ensure safety and minimize risks.

InChI:InChI=1/C15H14O2/c1-12-6-8-13(9-7-12)11-17-15-5-3-2-4-14(15)10-16/h2-10H,11H2,1H3

Upstream product

• 90-02-8 salicylaldehyde 
• 104-81-4 4-Methylbenzyl bromide 

Downstream Products

• 690969-91-6 C₁₅H₁₆O₂ 
• 94001-91-9 (2-hydroxymethylphenyl)(4-methylphenyl)methanol 

Relevant academic research and scientific papers

Copper-Catalyzed Asymmetric Diyne Cyclization via [1,2]-Stevens-Type Rearrangement for the Synthesis of Chiral Chromeno[3,4-c]pyrroles

Here, we report a copper-catalyzed asymmetric cascade cyclization/[1,2]-Stevens-type rearrangement via a non-diazo approach, leading to the practical and atom-economic assembly of various valuable chiral chromeno[3,4-c]pyrroles bearing a quaternary carbon

Synthesis of 2,3-Disubstituted Indoles and Benzofurans by the Tandem Reaction of Rhodium(II)-Catalyzed Intramolecular C-H Insertion and Oxygen-Mediated Oxidation

A highly effective and straightforward method to construct a wide range of functionalized 2,3-disubstituted indoles has been developed. The method involves the tandem reaction of rhodium(II)-catalyzed denitrogenative annulation of triazole-based benzyl an

Neighboring lithium-assisted [1,2]-wittig rearrangement: Practical access to diarylmethanol-based 1,4-diols and optically active binol derivatives with axial and sp3-central chirality

A facile and practical methodology for the synthesis of synthetically useful diarylmethanol-based 1,4-diols and enantiomerically pure BINOL-derived diols with axial and sp3-central chirality has been developed through neighboring lithium-promot