6249-79-2

Basic information

• Product Name: Ethanone, 1-(3-phenyloxiranyl)-
• CAS NO: 6249-79-2
• Molecular Formula: C10H10O2
• Molecular Weight: 162.188
• Mol File: 6249-79-2.mol
• Article Data: 53

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(3-phenyloxiranyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3-phenyloxiranyl)-(6249-79-2)
• EPA Substance Registry System: Ethanone, 1-(3-phenyloxiranyl)-(6249-79-2)

Safety Data

• Hazardous Substances Data: 6249-79-2(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-(3-phenyloxiranyl)- is a chemical compound that is also known as 1-acetyl-3-phenyl-2,3-epoxypropane. It is a colorless liquid with a sweet, fruity odor. Ethanone, 1-(3-phenyloxiranyl)- is used in the production of various pharmaceuticals, including antiviral and antibacterial agents. It is also used in the synthesis of certain fragrances and as a flavoring agent in foods and beverages. Additionally, it is a key intermediate in the preparation of other organic compounds, such as resins and polymers. Despite its useful applications, ethanone, 1-(3-phenyloxiranyl)- should be handled with caution as it may be harmful if ingested or inhaled in high concentrations.

Upstream product

• 100-52-7 benzaldehyde 
• 78-95-5 chloroacetone 
• 1896-62-4 (E)-benzalacetone 
• 598-31-2 1-bromoacetone 
• 19202-21-2 1-trans-cinnamoylpyrrolidine 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 536-74-3 phenylacetylene 
• 104974-60-9 rac-(Z)-4-phenylbut-3-en-2-ol 
• 73922-81-3 4-phenyl-but-3-yn-2-ol 
• 84033-94-3 (3R,4S)-3-Bromo-4-hydroxy-4-phenyl-butan-2-one 
• 937-53-1 (Z)-4-phenylbut-3-en-2-one 
• 19190-80-8 methyl 3-Phenylglycidate 
• 16812-43-4 bis(trimethylstannyl)methane 
• 53309-95-8 (+/-)-2-amino-4-phenylbut-3-ene 

Downstream Products

• 46904-25-0 2-benzylidene-3-methyl-2H-benzo[1,4]thiazine 
• 67-56-1 methanol 
• 4426-63-5 1-(3-Phenyloxiran-2-yl)ethanol 
• 38087-02-4 1-phenylbutane-2,3-dione 
• 5381-93-1 1-hydroxy-1-phenyl-3-butanone 
• 65469-88-7 1-phenylbutane-1,3-diol 
• 5355-63-5 3-hydroxy-4-phenyl-2-butanone 
• 5381-89-5 1-phenylbutane-2,3-diol 
• 63726-68-1 3-Oxo-2-phenylbutanal 
• 65-85-0 benzoic acid 
• 127-17-3 2-oxo-propionic acid 
• 100-52-7 benzaldehyde 

Relevant articles and documents

An efficient Darzens reaction promoted by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)

An efficient DBU promoted Darzens reaction utilising α-haloketones containing an enolizable α′-hydrogen is reported. This method diastereoselectively afforded the corresponding α,β-epoxy ketones good to excellent yields in an one-pot reaction without using any transition metals or additives. Furthermore, haloketones without an α′-hydrogen are also applicable in this reaction.

Stereodivergent Access to Enantioenriched Epoxy Alcohols with Three Stereogenic Centers via Ruthenium-Catalyzed Transfer Hydrogenation

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Biomimetic Oxidative Deamination Catalysis via ortho-Naphthoquinone-Catalyzed Aerobic Oxidation Strategy

An ortho-naphthoquinone-catalyzed oxidative deamination reaction has been developed where the molecular oxygen and water serve as the sole oxidant and nucleophile. The current aerobic deamination reaction proceeds via the ketimine formation between ortho-naphthoquinones and amines followed by the prototropic rearrangement and hydrolysis by water, representing a biomimetic oxidative deamination of amine species in the human body by the liver and kidneys. The compatibility of ortho-naphthoquinone organocatalysts with molecular oxygen and water opens up a new biomimetic catalyst system that can function as versatile deaminases for a variety of amine-containing molecules such as amino acids and DNA nuclear bases.