32046-97-2

Basic information

• Product Name: (4-methylphenyl)(3-phenyloxiran-2-yl)methanone
• CAS NO: 32046-97-2
• Molecular Formula: C₁₆H₁₄O₂
• Molecular Weight: 238.2812
• Mol File: 32046-97-2.mol
• Article Data: 50

Chemical Properties

• Boiling Point: 394.1°C at 760 mmHg
• Flash Point: 181.1°C
• Density: 1.181g/cm³
• Vapor Pressure: 2.02E-06mmHg at 25°C
• Refractive Index: 1.607
• CAS DataBase Reference: (4-methylphenyl)(3-phenyloxiran-2-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-methylphenyl)(3-phenyloxiran-2-yl)methanone(32046-97-2)
• EPA Substance Registry System: (4-methylphenyl)(3-phenyloxiran-2-yl)methanone(32046-97-2)

Safety Data

• Hazardous Substances Data: 32046-97-2(Hazardous Substances Data)

Usage

Description

(4-methylphenyl)(3-phenyloxiran-2-yl)methanone is a chemical compound with a molecular formula C17H16O2. It is a ketone containing a substituted phenyl and phenyloxirane functional group. (4-methylphenyl)(3-phenyloxiran-2-yl)methanone is known for its diverse chemical structure and reactivity, making it a valuable tool in various fields of science and industry.

Uses

Used in Pharmaceutical Industry:
(4-methylphenyl)(3-phenyloxiran-2-yl)methanone is used as a reagent or intermediate in organic synthesis for the development of new drugs. Its unique chemical structure and reactivity contribute to the creation of potential pharmaceutical compounds.
Used in Agrochemical Industry:
In the agrochemical field, (4-methylphenyl)(3-phenyloxiran-2-yl)methanone serves as a reagent or intermediate in the synthesis of pesticides. Its properties allow for the development of effective and novel agrochemical products.
Used in Materials Science:
(4-methylphenyl)(3-phenyloxiran-2-yl)methanone is utilized as a component in the research and development of advanced materials. Its versatility in chemical reactions enables the creation of innovative materials with specific properties for various applications.
It is important to handle (4-methylphenyl)(3-phenyloxiran-2-yl)methanone with care due to its potential hazards and toxic properties. However, when used appropriately, this compound offers significant potential in laboratory research and industrial applications.

Upstream product

• 4224-96-8 3-phenyl-1-p-tolylprop-2-en-1-one 
• 14802-30-3 (E)-1-(4-methylphenyl)-3-phenyl-2-propen-1-one 
• 100-52-7 benzaldehyde 
• 122-00-9 para-methylacetophenone 
• 94-41-7 benzalacetophenone 
• 100-42-5 styrene 
• 104-87-0 4-methyl-benzaldehyde 
• 14531-55-6 3,5-dimethyl-4-nitro-1H-pyrazole 
• 32046-97-2 1-p-methylphenyl-3-phenyl-2,3-epoxy-1-propanone 
• 124-38-9 carbon dioxide 
• 619-41-0 4-(bromoacetyl)toluene 

Downstream Products

• 51813-20-8 2-hydroxy-3-morpholin-4-yl-3-phenyl-1-p-tolyl-propan-1-one 
• 132455-52-8 (2R,3S)-3-Phenyl-oxirane-2-carboxylic acid p-tolyl ester 
• 76283-68-6 2-Hydroxy-3-phenyl-3-thiocyanato-1-p-tolyl-propan-1-one 
• 29329-38-2 5-phenyl-3-(p-tolyl)isoxazole 
• 134853-09-1 2-(Hydroxy-phenyl-methyl)-1-p-tolyl-pent-4-en-1-one 
• 132455-52-8 trans-4-methylphenyl 2,3-epoxy-3-phenylpropanoate 
• 135460-25-2 3-Bromo-2-hydroxy-3-phenyl-1-p-tolyl-propan-1-one 
• 99430-33-8 3-Fluoro-2-hydroxy-3-phenyl-1-p-tolyl-propan-1-one 
• 32047-09-9 3-Chloro-2-hydroxy-3-phenyl-1-p-tolyl-propan-1-one 
• 32047-09-9 3-Chloro-2-hydroxy-3-phenyl-1-p-tolyl-propan-1-one 
• 21866-07-9 1,5-Bis-(p-tolyl)-3-phenyl-2,4-bis-phenylmercaptopentan-1,5-dion 
• 32047-03-3 1-(4-methylphenyl)-3-phenylpropan-1,2-dione 
• 4079-54-3 2-hydroxy-1-p-tolyl-ethanone 
• 30152-31-9 3-(4?'-methylphenyl)-5-phenyl-1H-pyrazole 

Relevant articles and documents

A high-yielding protocol for the synthesis of 4,5-diarylpyrimidin-2-amine derivatives from chalcones

A novel, high yielding and versatile protocol was achieved for the synthesis of 4,5-diaryl-2-pyrimidinamine derivatives from chalcones. The synthesis was accomplished by converting the chalcones into 3-chloro-2,3-diaryl-2-propen-1-ones followed by subsequent reaction with amidine derivatives.

Asymmetric epoxidation of α,β-unsaturated ketones catalyzed by rare-earth metal amides RE[N(SiMe3)2]3with chiral TADDOL ligands

The catalytic asymmetric epoxidation of α,β-unsaturated ketones by tert-butylhydroperoxide (TBHP) has been well established using rare-earth metal amides RE[N(SiMe3)2]3 (RE = La(1), Nd(2), Sm(3), Y(4), Yb(5)) with chiral TADDOL ligands. It was found that

Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Using Amide-Based Cinchona Alkaloids as Hybrid Phase-Transfer Catalysts

A series of 20 one chiral epoxides were obtained with excellent yields (up to 99%) and enantioselectivities (up to >99% ee) using hybrid amide-based Cinchona alkaloids. Our method is characterized by low catalyst loading (0.5 mol %) and short reaction times. Moreover, the epoxidation process can be carried out in 10 cycles, without further catalyst addition to the reaction mixture. This methodology significantly enhance the scale of the process using very low catalyst loading.