23012-25-1

Basic information

• Product Name: Ethanone, 1-(2,4-dimethyl-5-oxazolyl)- (9CI)
• Synonyms: Ethanone, 1-(2,4-dimethyl-5-oxazolyl)- (9CI);5-Acetyl-2,4-diMethyloxazole;1-(2,4-Dimethyl-1,3-oxazol-5-yl)ethan-1-one, 2,4-Dimethyl-5-ethanoyl-1,3-oxazole;5-Acetyl-2,4-dimethyl-1,3-oxazole
• CAS NO: 23012-25-1
• Molecular Formula: C₇H₉NO₂
• Molecular Weight: 139.15186
• Product Categories: ACETYLGROUP
• Mol File: 23012-25-1.mol
• Article Data: 10

Chemical Properties

• Melting Point: 170-172°C
• Boiling Point: 212.4 °C at 760 mmHg
• Flash Point: 82.2 °C
• Appearance: /
• Density: 1.074 g/cm³
• Vapor Pressure: 0.174mmHg at 25°C
• Refractive Index: 1.472
• CAS DataBase Reference: Ethanone, 1-(2,4-dimethyl-5-oxazolyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(2,4-dimethyl-5-oxazolyl)- (9CI)(23012-25-1)
• EPA Substance Registry System: Ethanone, 1-(2,4-dimethyl-5-oxazolyl)- (9CI)(23012-25-1)

Safety Data

• Hazardous Substances Data: 23012-25-1(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-(2,4-dimethyl-5-oxazolyl)- (9CI), also known as dimethylaminomethylacetophenone, is a chemical compound with the molecular formula C10H11NO2. It is a ketone derivative that contains an oxazole ring, which makes it a part of the heterocyclic compound family. This chemical is commonly used as a reagent in organic synthesis and pharmaceutical research, particularly in the development of new drugs. It has also been studied for its potential antifungal and antibacterial properties. Additionally, it is used in the production of fragrances and flavorings. However, it is important to handle this compound with care, as it may be harmful if ingested, inhaled, or absorbed through the skin.

InChI:InChI=1/C7H9NO2/c1-4-7(5(2)9)10-6(3)8-4/h1-3H3

Upstream product

• 23652-91-7 (Z)-1-methyl-1-(N-acetyl)amino-2-acetylethylene 
• 123-54-6 acetylacetone 
• 69062-86-8 2,4-dimethyloxazole-5-carbaldehyde 
• 631-61-8 ammonium acetate 
• 1694-29-7 3-chloropentane-2,4-dione 
• 60-35-5 acetamide 

Downstream Products

• 71267-12-4 2,4,6-trimethyl-5-hydroxypyrimidine 
• 1616100-76-5 (R)-N-((2S,4R)-2-(2,4-difluoro-5-(pyrimidin-5-yl)phenyl)-4-(2,4-dimethyloxazol-5-yl)-4-hydroxybutan-2-yl)-2-methylpropane-2-sulfinamide 
• 1616100-77-6 (1R,3S)-3-amino-3-(2,4-difluoro-5-(pyrimidin-5-yl)phenyl)-1-(2,4-dimethyloxazol-5-yl)butan-1-ol 
• 1616100-78-7 N-(((2S,4R)-2-(2,4-difluoro-5-(pyrimidin-5-yl)phenyl)-4-(2,4-dimethyloxazol-5-yl)-4-hydroxybutan-2-yl)carbamothioyl)benzamide 
• 1616100-26-5 (4S,6S)-4-(2,4-difluoro-5-(pyrimidin-5-yl)phenyl)-6-(2,4-dimethylisoxazol-5-yl)-4-methyl-5,6-dihydro-4H-1,3-thiazin-2-amine 
• 1616100-75-4 (R)-N-((S)-2-(2,4-difluoro-5-(pyrimidin-5-yl)phenyl)-4-(2,4-dimethyloxazol-5-yl)-4-oxobutan-2-yl)-2-methylpropane-2-sulfinamide 
• 1377837-78-9 3-[4-(2,4-Dimethyl-oxazol-5-yl)-thiazol-2-ylamino]-4-isopropoxy-benzamide 
• 19615-50-0 ethyl 2-methyl-5-acetylfuran-3-carboxylate 

Relevant articles and documents

Generation of Dimethyl Sulfoxide Coordinated Thermally Stable Halogen Cation Pools for C?H Halogenation

A method to generate halogen cation pools from the reaction of 1,2-dihaloethanes (hal=Br, I) and dimethyl sulfoxide (DMSO) for C?H halogenation of arenes and heteroarenes was reported. The initial reaction of DMSO and 1,2-dihaloethane generates the sulfur

OPIOID RECEPTOR MODULATORS AND USE THEREOF

Disclosed is an in vitro screening method for identifying an antagonist-to-agonist allosteric modifier of a mu-opioid receptor and an in vivo method for confirming that a test compound is such a modifier of a mu-opioid receptor. Also disclosed is a method

Synthesis of oxazoles from enamides via phenyliodine diacetate-mediated intramolecular oxidative cyclization

A group of functionalized oxazoles were synthesized in moderate to good yields from enamides via phenyliodine diacetate (PIDA)-mediated intramolecular cyclization. The main advantageous features of the present method include its broad substrate scope and the heavy-metal-free characteristic of the oxidative carbon-oxygen bond formation process.