1036715-60-2

Basic information

• Product Name: Methyl 4-acetyl-2-Methylbenzoate
• Synonyms: Methyl 4-acetyl-2-Methylbenzoate
• CAS NO: 1036715-60-2
• Molecular Formula: C₁₁H₁₂O₃
• Molecular Weight: 192.21118
• EINECS: -0
• Mol File: 1036715-60-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 4-acetyl-2-Methylbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 4-acetyl-2-Methylbenzoate(1036715-60-2)
• EPA Substance Registry System: Methyl 4-acetyl-2-Methylbenzoate(1036715-60-2)

Safety Data

• Hazardous Substances Data: 1036715-60-2(Hazardous Substances Data)

Usage

General Description

Methyl 4-acetyl-2-Methylbenzoate, also known as 4-acetyl-2-Methylbenzoic acid methyl ester, is a chemical compound that belongs to the class of organic compounds known as benzoyl esters. It is used in various industrial processes and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It has a strong odor and is flammable, and therefore requires careful handling. Methyl 4-acetyl-2-Methylbenzoate is commonly used in the flavor and fragrance industry, and it is also utilized in the production of cosmetics and personal care products. Its chemical structure consists of a benzene ring with a methyl group and an acetyl group attached at specific positions, allowing for a wide range of potential reactions and applications.

Upstream product

• 369-32-4 1-(4-fluoro-3-methylphenyl)ethanone 
• 95-52-3 2-Fluorotoluene 
• 99548-55-7 4-bromo-2-methyl-benzoic acid methyl ester 
• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 37074-40-1 1-(4-bromo-3-methylphenyl)ethan-1-one 
• 51930-77-9 1-(4-bromo-3-methylphenyl)ethan-1-ol 
• 78775-11-8 3-methyl-4-bromobenzaldehyde 
• 55860-35-0 4-acetyl-2-methyl benzoic acid 
• 3637-01-2 3,4-dimethylacetophenone 

Downstream Products

• 1391709-79-7 C₁₈H₁₅FO₃ 
• 1391709-90-2 4-(5-(4-fluorophenyl)-4,5-dihydro-1H-pyrazol-3-yl)-2-methylbenzohydrazide 
• 1391709-74-2 C₁₈H₁₅ClO₃ 
• 1391709-78-6 C₁₈H₁₅ClO₃ 
• 1391709-89-9 4-(5-(2-chlorophenyl)-4,5-dihydro-1H-pyrazol-3-yl)-2-methylbenzohydrazide 
• 1391709-70-8 C₁₈H₁₅NO₅ 
• 1391709-75-3 C₁₈H₁₅NO₅ 
• 1391709-76-4 C₁₈H₁₆O₃ 
• 1391709-87-7 4-(4,5-dihydro-5-phenyl-1H-pyrazol-3-yl)-2-methylbenzohydrazide 
• 1391709-71-9 C₁₈H₁₆O₄ 
• 1391709-77-5 C₁₉H₁₈O₄ 
• 1391709-88-8 4-(4,5-dihydro-5-(4-methoxyphenyl)-1H-pyrazol-3-yl)-2-methylbenzohydrazide 
• 1391709-69-5 C₁₈H₁₆O₄ 
• 1391709-73-1 C₁₉H₁₈O₅ 

Relevant articles and documents

Catalytic Enantioselective Direct Aldol Addition of Aryl Ketones to α-Fluorinated Ketones

The catalytic enantioselective synthesis of α-fluorinated chiral tertiary alcohols from (hetero)aryl methyl ketones is described. The use of a bifunctional iminophosphorane (BIMP) superbase was found to facilitate direct aldol addition by providing the strong Br?nsted basicity required for rapid aryl enolate formation. The new synthetic protocol is easy to perform and tolerates a broad range of functionalities and heterocycles with high enantioselectivity (up to >99:1 e.r.). Multi-gram scalability has been demonstrated along with catalyst recovery and recycling. 1H NMR studies identified a 1400-fold rate enhancement under BIMP catalysis, compared to the prior state-of-the-art catalytic system. The utility of the aldol products has been highlighted with the synthesis of various enantioenriched building blocks and heterocycles, including 1,3-aminoalcohol, 1,3-diol, oxetane, and isoxazoline derivatives.

Modulators of methyl modifying enzymes, compositions and uses thereof

Agents for modulating methyl modifying enzymes, compositions and uses thereof are provided herein.

MODULATORS OF METHYL MODIFYING ENZYMES, COMPOSITIONS AND USES THEREOF

Agents for modulating methyl modifying enzymes, compositions and uses thereof are provided herein