79383-44-1

Basic information

• Product Name: METHYL 2-METHOXY-6-METHYLBENZOATE
• Synonyms: METHYL 2-METHOXY-6-METHYLBENZOATE;2-Methoxy-6-Methyl-benzoic acid Methyl ester;Benzoic acid, 2-Methoxy-6-Methyl-, Methyl ester
• CAS NO: 79383-44-1
• Molecular Formula: C₁₀H₁₂O₃
• Molecular Weight: 180.2
• EINECS: 1806241-263-5
• Mol File: 79383-44-1.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 95-96 °C(Press: 0.5 Torr)
• Appearance: /
• Density: 1.075±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: METHYL 2-METHOXY-6-METHYLBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-METHOXY-6-METHYLBENZOATE(79383-44-1)
• EPA Substance Registry System: METHYL 2-METHOXY-6-METHYLBENZOATE(79383-44-1)

Safety Data

• Hazardous Substances Data: 79383-44-1(Hazardous Substances Data)

Usage

General Description

Methyl 2-methoxy-6-methylbenzoate is a chemical compound with the molecular formula C10H12O3. It is commonly used as a flavoring agent in the food and beverage industry due to its sweet, fruity aroma. It is also used in the manufacturing of fragrance and cosmetic products. This chemical is a clear, colorless liquid with a strong odor and is soluble in alcohol and ether. It is important to handle this chemical with care and follow safety guidelines as it can cause skin and eye irritation and should be stored in a cool, well-ventilated area away from direct sunlight and heat sources.

Upstream product

• 186581-53-3 diazomethane 
• 124-38-9 carbon dioxide 
• 100-84-5 1-methoxy-3-methyl-benzene 
• 67-56-1 methanol 
• 50463-84-8 2-methoxy-6-methylbenzoyl chloride 
• 33528-09-5 methyl 6-methylsalicylate 
• 77-78-1 dimethyl sulfate 
• 2944-49-2 2,3-dimethylanisole 
• 6161-65-5 2-methoxy-6-methyl-benzoic acid 
• 4389-50-8 2-amino-6-methylbenzoic acid 
• 18595-13-6 2-amino-6-methylbenzoic acid methyl ester 
• 61940-22-5 methyl 2-methyl-6-nitrobenzoate 
• 13506-76-8 2-methyl-6-nitrobenzoic acid 
• 567-61-3 2-hydroxy-6-methylbenzoic acid 

Downstream Products

• 186670-53-1 methyl 2-methoxy-6-(8-nonynyl)benzoate 
• 1601496-83-6 C₅₂H₆₀N₆O₈ 
• 1601496-84-7 C₅₂H₆₀N₆O₈ 
• 1601495-60-6 C₅₂H₅₄N₆O₉ 
• 1601495-61-7 C₅₂H₅₄N₆O₉ 
• 1601495-62-8 C₅₆H₆₆N₂O₉ 
• 1601495-63-9 C₅₆H₆₆N₂O₉ 
• 1601495-59-3 C₅₂H₅₆N₆O₉ 
• 89244-39-3 (2-methoxy-6-methylphenyl)methanol 
• 13185-18-7 8-methoxy-1-tetralone 
• 133379-08-5 methyl 3-bromo-2-(bromomethyl)-6-methoxybenzoate 

Relevant articles and documents

Preparation method of 2-methoxy-6-methylbenzoic acid

The invention discloses a synthesis process of 2-methoxy-6-methylbenzoic acid, which comprises the following steps: (1) reduction hydrogenation reaction: by taking 2-methyl-6-nitrobenzoic acid or methyl 2-methyl-6-nitrobenzoate as a raw material, methanol as a solvent, hydrogen as a hydrogen source and palladium on carbon or platinum on carbon as a catalyst, carrying out hydrogenation reduction to prepare 2-amino-6-methylbenzoic acid or methyl 2-amino-6-methylbenzoate; (2) diazotization, hydrolysis and esterification one-pot reaction: by taking the reduction product as a raw material, and methanol as a solvent, performing diazotization, hydrolysis and esterification reaction under the action of a diazotization reagent to prepare methyl 2-hydroxy-6-methylbenzoate; (3) methylation reaction: with methyl 2-hydroxy-6-methylbenzoate as a raw material and dimethyl sulfate as a methylation reagent, carrying out methylation reaction in the presence of alkali to prepare methyl 2-methoxy-6-methylbenzoate; and (4) hydrolysis reaction: mixing the methyl 2-methoxy-6-methylbenzoate with alkali and water, conducting heating for hydrolysis, conducting cooling after the reaction is completed, adjusting the pH value to 1-3 by using acid, separating out a product, and conducting filtering and drying to obtain the 2-methoxy-6-methylbenzoic acid.

Copper-Catalyzed One-Pot Synthesis of Dibenzofurans, Xanthenes, and Xanthones from Cyclic Diphenyl Iodoniums

Oxygenation of cyclic diphenyl iodoniums (CDPIs) with varied medium-ring sizes has been fully investigated. This practical copper-catalyzed tandem reaction of CDPIs with water as the oxygen source enables the construction of derivatised dibenzofurans and xanthenes at moderate to good yields. Moreover, structurally important xanthones are also successfully accessed under the oxygenation conditions with additional TEMPO.

HISTONE ACETYLTRANSFERASE ACTIVATORS AND COMPOSITIONS AND USES THEREOF

The invention provides pharmaceutical compositions and methods for treating cancer, neurodegenerative disorders, conditions associated with accumulated amyloid-beta peptide deposits, Tau protein levels, and/or accumulations of alpha-synuclein by administering a HAT modulator and a HDAC modulator to a subject.