90674-26-3

Basic information

• Product Name: 3-METHOXY-5-METHYLBENZALDEHYDE
• Synonyms: 3-METHOXY-5-METHYLBENZALDEHYDE
• CAS NO: 90674-26-3
• Molecular Formula: C₉H₁₀O₂
• Molecular Weight: 150.18
• Mol File: 90674-26-3.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 85 °C(Press: 2 Torr)
• Appearance: /
• Density: 1.062±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 3-METHOXY-5-METHYLBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHOXY-5-METHYLBENZALDEHYDE(90674-26-3)
• EPA Substance Registry System: 3-METHOXY-5-METHYLBENZALDEHYDE(90674-26-3)

Safety Data

• Hazardous Substances Data: 90674-26-3(Hazardous Substances Data)

Usage

General Description

3-Methoxy-5-methylbenzaldehyde is a chemical compound with the molecular formula C9H10O2. It is a pale yellow liquid that is commonly used in the fragrance and flavor industry as a synthetic aroma compound. It has a strong floral and sweet odor, and is often used in perfumes, soaps, and other personal care products. It is also used as a flavoring agent in food products, adding a sweet and floral note to the final product. Additionally, it has been studied for its potential medicinal properties, including its role as an antimicrobial agent and for its potential anti-inflammatory effects.

Upstream product

• 106116-42-1 1-bromomethyl-3-methoxy-5-methyl-benzene 
• 50-00-0 formaldehyd 
• 66584-31-4 3-methoxy-5-methylphenylamine 
• 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 
• 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 

Downstream Products

• 929567-61-3 1-(3-methoxy-5-methylphenyl)ethanol 
• 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 articles and documents

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.

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).

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