14894-74-7

Usage

Uses

Used in Flavor and Fragrance Industry:
2,4,5-Trimethoxy toluene is used as a flavoring agent for its sweet and floral scent, making it suitable for incorporation into food products. It is also used in the fragrance industry to add a pleasant aroma to perfumes, soaps, and cosmetics.
Used in Pharmaceutical Industry:
Due to its aromatic properties, 2,4,5-Trimethoxy toluene has potential applications in the pharmaceutical industry. However, it is important to note that it may pose health risks and should be handled and used with caution.

InChI:InChI=1/C10H14O3/c1-7-5-9(12-3)10(13-4)6-8(7)11-2/h5-6H,1-4H3

Upstream product

• 14469-99-9 [1-(2,4,5-Trimethoxy-phenyl)-meth-(Z)-ylidene]-hydrazine 
• 135-77-3 1,2,4-trimethoxy-benzene 
• 30038-31-4 (2,4,5-trimethoxyphenyl)methanol 
• 490-64-2 asaronic acid 
• 138865-88-0 1,2,4-trimethoxy-5-methyl-3-trimethylsilyl-6-(propylthio)benzene 
• 4460-86-0 asaraldehyde 
• 7721-61-1 2-methyl-4-methoxy-5-hydroxybenzaldehyde 
• 7721-62-2 4,5-dimethoxy-2-methylbenzaldehyde 
• 93-51-6 2-Methoxy-4-methylphenol 
• 77-78-1 dimethyl sulfate 
• 78238-02-5 4-methoxy-6-methylbenzene-1,3-diol 
• 74-88-4 methyl iodide 
• 72312-07-3 2-hydroxy-4,5-dimethoxytoluene 
• 138865-90-4 1,2,4-trimethoxy-3-trimethylsilyl-5-methylbenzene 

Downstream Products

• 490-64-2 asaronic acid 
• 138865-90-4 1,2,4-trimethoxy-3-trimethylsilyl-5-methylbenzene 
• 4460-86-0 asaraldehyde 
• 1186001-58-0 C₁₄H₁₃NO₂ 
• 614-13-1 2-methoxy-5-methyl-1,4-benzoquinone 

Relevant academic research and scientific papers

An expedient synthesis of murrayaquinone A via a novel oxidative free radical reaction

Murrayaquinones A–D is a group of four bioactive carbazole-1,4-dione natural products isolated from the root bark of the plant Murraya eucrestifolia hayata. Murrayaquinone is synthesized in five steps starting from the commercially available 2,4,5-trimeth

Alkylbenzoquinone involved in development of cellular slime molds

The structure of the prespore-cell-promoting factor from Dictyostelium discoideum was determined to be 2-hydroxy-5-methyl-6-pentylbenzoquinone. The synthetic compound has prespore-cell-promoting activity similar to the natural one, with half-maximal induction at a concentration as low as 40 pM. It was also found that the factor induces aggregation in an aggregation-deficient mutant of a related species, Polysphodilium violaceum. Both these activities are sensitive to positional isomerism with the 6-methyl-5-pentyl isomer showing no detectable activity.

The Huang-Minlon modification of Wolff-Kishner reduction in rapid and simple way using microwave technology

A high yielding, simple and fast method for the reduction of various aldehydes and ketones to the respective hydrocarbons following Huang-Minlon modification tender microwave irradiation is described.

Metalation reactions. XVI. Polylithiation of 1,3,5- and 1,2,4-trimethoxybenzene

Polylithiation reactions of 1,3,5- and 1,2,4-trimethoxybenzenes have been investigated. Results showed that it is possible to substitute all arylic hydrogens through one-pot sequential bimetalation/monometalation, monometalation/bimetalation or three mono

INTRODUCTION OF A HYDROXYL GROUP INTO THE CREOSOL MOLECULE

The introduction of a hydroxyl group into the molecule of 2-methoxy-4-methylphenol through Rieche formylation and Baeyer-Villiger oxidation was investigated.With dichloromethyl methyl ether meta-formylation of creosol occurs.