105041-52-9

Usage

Uses

Used in Pharmaceutical Industry:
2,4,6-trimethyl-3-(chloromethyl)benzaldehyde is utilized as an intermediate in the synthesis of various pharmaceuticals. Its aromatic properties and reactivity due to the chloromethyl group make it a valuable component in the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4,6-trimethyl-3-(chloromethyl)benzaldehyde serves as a key intermediate in the production of agrochemicals. Its versatility in chemical reactions allows for the creation of effective compounds for agricultural applications.
Used in Fragrance and Flavoring Industry:
2,4,6-trimethyl-3-(chloromethyl)benzaldehyde is employed as a component in the production of fragrances and flavorings. Its aromatic nature contributes to the creation of unique scents and tastes in various consumer products.
Used in Organic Synthesis:
2,4,6-trimethyl-3-(chloromethyl)benzaldehyde is also used in organic synthesis processes due to its reactivity and the presence of the chloromethyl group, which allows for a wide range of chemical reactions, leading to the formation of diverse organic compounds.

Upstream product

• 4885-02-3 Dichloromethyl methyl ether 
• 733-07-3 dimesitylmethane 
• 1585-16-6 2-chloromethyl-1,3,5-trimethylbenzene 
• 108-67-8 1,3,5-trimethyl-benzene 
• 50-00-0 formaldehyd 
• 487-68-3 mesytaldehyde 

Downstream Products

• 52411-49-1 3-(chloromethyl)-2,4,6-trimethylbenzoic acid 
• 179554-09-7 2,4,6-trimethyl-3-morpholin-4-yl-methylbenzaldehyde 
• 137380-49-5 (hydroxymethyl)formylmesitylene 
• 88339-51-9 methoxymethylformylmesitylene 
• 134284-58-5 3-chloromethyl-2,4,6-trimethylbenzylidene dichloride 
• 137380-48-4 acetoxymethylformylmesitylene 
• 137380-47-3 (β-methoxyethoxymethyl)formylmesitylene 

Relevant academic research and scientific papers

1,3-dipolar compound bearing an imidazole functional group

In a 1,3-dipolar compound of formula Q-A-B, Q comprises a dipole containing at least and preferably one nitrogen atom, A, which is preferably divalent, is an atom or a group of atoms connecting Q to B, and B comprises an imidazole ring. An unsaturated polymer modified by grafting the 1,3-dipolar compound is also disclosed.

SYNTHESIS OF STERICALLY HINDERED AROMATIC ALDEHYDES

Formylation of mesitylene, durene, and m-xylene derivatives containing electron-donor and electron-acceptor substituents by dichloromethyl methyl ether was studied in the presence of TiCl4.A series of functionally substituted sterically hindered benzaldehydes was prepared from the products of these reactions.

NEW DATA ON THE FORMYLATION OF MESITYLENE AND DIMESITYLMETHANE BY DICHLOROMETHYL ETHER

During the formylation of mesitylene by the action of dichloromethyl methyl ether in the presence of aluminium chloride or titanium tetrachloride an appreciable amount of 2,4,6-trimethylbenzylidene chloride is formed.This indicates the possible appearance of the CHCl2+ cation as intermediate particle.The disubstituted products are formed in addition to the monosubstitution products.In addition to the corresponding dialdehyde, the formylation of dimesitylmethane leads to the formation of products which contain one benzene ring and appear during cleavage of thesubstrate and subsequent substitution (formylmesitylene, dichloromethylmesitylene, chloromethylmesitylenecarbaldehyde, chloromethyl-2,4,6-trimethylbenzylidene chloride).