41204-59-5

Basic information

• Product Name: 4-METHOXY-2'-METHYLBENZOPHENONE
• Synonyms: 4-METHOXY-2'-METHYLBENZOPHENONE;UKRORGSYN-BB BBV-5119100
• CAS NO: 41204-59-5
• Molecular Formula: C₁₅H₁₄O₂
• Molecular Weight: 226.27
• Mol File: 41204-59-5.mol
• Article Data: 39

Chemical Properties

• Boiling Point: 336.9°C at 760 mmHg
• Flash Point: 144.3°C
• Appearance: /
• Density: 1.088g/cm³
• Vapor Pressure: 0.000108mmHg at 25°C
• Refractive Index: 1.563
• CAS DataBase Reference: 4-METHOXY-2'-METHYLBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXY-2'-METHYLBENZOPHENONE(41204-59-5)
• EPA Substance Registry System: 4-METHOXY-2'-METHYLBENZOPHENONE(41204-59-5)

Safety Data

• Hazardous Substances Data: 41204-59-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H14O2/c1-11-5-3-4-6-14(11)15(16)12-7-9-13(17-2)10-8-12/h3-10H,1-2H3

Upstream product

• 100-66-3 methoxybenzene 
• 607-86-3 2-methylbenzoic anhydride 
• 16419-60-6 2-Methylphenylboronic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-07-2 4-methoxy-benzoyl chloride 
• 108-88-3 toluene 
• 93296-09-4 4-methoxyphenylzinc chloride 
• 933-88-0 ortho-toluoyl chloride 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 696-62-8 para-iodoanisole 
• 1227475-35-5 (methyl)bis(2-tolyl)silane 
• 24890-62-8 1-(1-(4-methoxyphenyl)vinyl)-2-methylbenzene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 529-20-4 2-methylphenyl aldehyde 

Downstream Products

• 50439-04-8 [2-(4-methoxy-benzoyl)-phenyl]-acetic acid 
• 220583-41-5 4-methoxyphenyl(2-methylphenyl)methanol 

Relevant articles and documents

Photo-induced oxidative cleavage of C-C double bonds for the synthesis of biaryl methanoneviaCeCl3catalysis

A Ce-catalyzed strategy is developed to produce biaryl methanonesviaphotooxidative cleavage of C-C double bonds at room temperature. This reaction is performed under air and demonstrates high activity as well as functional group tolerance. A synergistic Ce/ROH catalytic mechanism is also proposed based on the experimental observations. This protocol should be the first successful Ce-catalyzed photooxidation reaction of olefins with air as the oxidant, which would provide inspiration for the development of novel Ce-catalyzed photochemical synthesis processes.

Silylcarboxylic Acids as Bifunctional Reagents: Application in Palladium-Catalyzed External-CO-Free Carbonylative Cross-Coupling Reactions

A palladium-catalyzed external-CO-free carbonylative Hiyama-Denmark cross-coupling reaction is presented. The introduction of silylcarboxylic acids as bifunctional reagents (CO and nucleophile source) avoids the need for external gaseous CO and a silylarene coupling partner. The transformation features high functional group tolerance and it is successful with electron-rich, -neutral, and -poor aryl iodides. Stoichiometric studies and control experiments provide insight into the reaction mechanism and support the hypothesized dual role of silylcarboxylic acids. (Figure presented.).

Arylation of Aldehydes to Directly Form Ketones via Tandem Nickel Catalysis

A nickel-catalyzed arylation of both aliphatic and aromatic aldehydes proceeds with air-stable (hetero)arylboronic acids, with an exceptionally wide substrate scope. The neutral condition tolerates acidic hydrogen and sensitive polar groups and also preserves α-stereocenters of some chiral aldehydes. Interestingly, this nickel(0) catalysis does not follow common 1,2-insertion of arylmetal species to aldehydes and β-hydrogen elimination.