90674-26-3

Usage

Uses

Used in Fragrance Industry:
3-METHOXY-5-METHYLBENZALDEHYDE is used as a synthetic aroma compound for its strong floral and sweet scent, enhancing the olfactory appeal of perfumes, soaps, and other personal care products.
Used in Flavor Industry:
In the flavor industry, 3-METHOXY-5-METHYLBENZALDEHYDE is used as a flavoring agent in food products, imparting a sweet and floral note to the final product, thereby enriching the taste experience.
Used in Medicinal Applications:
3-METHOXY-5-METHYLBENZALDEHYDE is studied for its potential medicinal properties, serving as an antimicrobial agent, which could be beneficial in treating various infections. Additionally, its potential anti-inflammatory effects are being explored for possible therapeutic uses in managing inflammation-related conditions.

Upstream product

• 119650-44-1 (3-methoxy-5-methylphenyl)methanol 
• 60549-26-0 3-hydroxy-5-methylbenzaldehyde 
• 74-88-4 methyl iodide 
• 74204-00-5 3-bromo-5-methylphenol 
• 1222188-59-1 1-methoxy-3-(methoxymethyl)-5-methylbenzene 
• 79-46-9 2-nitropropane 
• 106116-42-1 1-bromomethyl-3-methoxy-5-methyl-benzene 
• 62089-34-3 3-methoxy-5-methylbenzoic acid 
• 585-81-9 3-hydroxy-5-methylbenzoic acid 
• 108593-44-8 methyl 3-methoxy-5-methylbenzoate 
• 874-63-5 3,5-dimethylmethoxybenzene 
• 50-00-0 formaldehyd 
• 66584-31-4 3-methoxy-5-methylphenylamine 

Downstream Products

• 202195-05-9 2-bromo-3-methoxy-5-methylbenzaldehyde 
• 329788-96-7 2-(3-hydroxy-5-methylphenyl)-1,3-dioxane 
• 60549-26-0 3-hydroxy-5-methylbenzaldehyde 
• 1333950-31-4 C₂₃H₁₈N₆O 
• 1333950-41-6 (E)-3-(3-hydroxy-5-methylphenyl)acrylonitrile 
• 1333950-42-7 (E)-3-(3-methoxy-5-methylphenyl)acrylonitrile 
• 704-29-0 2-Amino-3-methoxy-5-methyl-benzaldehyd 
• 113649-28-8 2-(3,5-Dimethoxybenzyl)-2,3-dihydro-2-(3-methoxy-5-methylbenzyl)-7-methyl-1H-inden-1-on 
• 113649-27-7 2,3-Dihydro-2,2-bis(3-methoxy-5-methylbenzyl)-7-methyl-1H-inden-1-on 
• 113649-26-6 2,3-Dihydro-2-(3-methoxy-5-methylbenzyl)-7-methyl-1H-inden-1-on 

Relevant academic research and scientific papers

Selective Electrochemical Oxygenation of Alkylarenes to Carbonyls

An efficient electrochemical method for benzylic C(sp3)-H bond oxidation has been developed. A variety of methylarenes, methylheteroarenes, and benzylic (hetero)methylenes could be converted into the desired aryl aldehydes and aryl ketones in moderate to excellent yields in an undivided cell, using O2 as the oxygen source and lutidinium perchlorate as an electrolyte. On the basis of cyclic voltammetry studies, 18O labeling experiments, and radical trapping experiments, a possible single-electron transfer mechanism has been proposed for the electrooxidation reaction.

Volatiles from the xylarialean fungus Hypoxylon invadens

The volatiles emitted by agar plate cultures of the xylarialean fungus Hypoxylon invadens were investigated by use of a closed loop stripping apparatus in combination with GC-MS. Several aromatic compounds were found that could only be identified by comparison to all possible constitutional isomers with different ring substitution patterns. For the set of identified compounds a plausible biosynthetic scheme was suggested that gives further support for the assigned structures.

Selective Aerobic Oxidation of Methylarenes to Benzaldehydes Catalyzed by N-Hydroxyphthalimide and Cobalt(II) Acetate in Hexafluoropropan-2-ol

Efficient and highly selective catalytic conditions for the aerobic autoxidation of methylarenes to benzaldehydes, based on N-hydroxyphthalimide (NHPI) and cobalt(II) acetate in 1,1,1,3,3,3-hexafluoropropan-2-ol (HFIP), were developed. The sustainable conditions enable a multigram scale preparation of benzaldehyde derivatives in high efficiency and with excellent chemoselectivity (up to 99 % conversion and 98 % selectivity).

HETEROCYCLIC CARBOXYLIC ACIDS AS ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE

The present invention relates to compounds of formula I: and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R5, R6, R7, R8, R9, B, V, W, X, Y, Z and m are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.

AROMATIC RING COMPOUND

Provided is an aromatic ring compound having a GPR40 agonist activity. A compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof has a GPR40 agonist activity, and is useful as an agent for the prophylaxis or treatment of diabetes and the like.

ALKOXY PYRAZOLES AS SOLUBLE GUANYLATE CYCLASE ACTIVATORS

The present invention relates to compounds of formula (I): and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6 and R7 are as defined herein. The inventi

Roles of the synergistic reductive O-methyltransferase GilM and of O-methyltransferase GilMT in the gilvocarcin biosynthetic pathway

Two enzymes of the gilvocarcin biosynthetic pathway, GilMT and GilM, with unclear functions were investigated by in vitro studies using purified, recombinant enzymes along with synthetically prepared intermediates. The studies revealed GilMT as a typical

Efficient discovery of potent anti-HIV agents targeting the Tyr181Cys variant of HIV reverse transcriptase

Non-nucleoside reverse transcriptase inhibitors (NNRTIs) that interfere with the replication of human immunodeficiency virus (HIV) are being pursued with guidance from molecular modeling including free-energy perturbation (FEP) calculations for protein-in

An oxidation of benzyl methyl ethers with NBS that selectively affords either aromatic aldehydes or aromatic methyl esters

Either mono- or dibromination of benzyl methyl ethers can be achieved by controlling the amount of NBS and the temperature. Elimination of methyl bromide from the monobrominated intermediates produces aromatic aldehydes, whereas hydrolysis of the dibrominated intermediates affords aromatic methyl esters in good yields.

The first total synthesis of (±)-γ-herbertenol, a herbertene isolated from a non-herbertus source

The structure of the aromatic sesquiterpene, (±)-γ- herbertenol, the first herbertane to be isolated from a non-herbertus source, was confirmed by a total synthesis, employing a Claisen rearrangement and ring-closing metathesis. Georg Thieme Verlag Stuttg