378186-96-0

Basic information

• Product Name: 2,3-Butadien-1-one, 1-(4-bromophenyl)-
• CAS NO: 378186-96-0
• Molecular Formula: C10H7BrO
• Molecular Weight: 223.069
• Mol File: 378186-96-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2,3-Butadien-1-one, 1-(4-bromophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Butadien-1-one, 1-(4-bromophenyl)-(378186-96-0)
• EPA Substance Registry System: 2,3-Butadien-1-one, 1-(4-bromophenyl)-(378186-96-0)

Safety Data

• Hazardous Substances Data: 378186-96-0(Hazardous Substances Data)

Usage

Yellow liquid

2,3-Butadien-1-one, 1-(4-bromophenyl)is a yellow liquid, meaning it has a visible color and is in a liquid state at room temperature.

Pungent odor

This chemical has a pungent odor, meaning it has a strong and possibly unpleasant smell.

Building block for various compounds

It is primarily used in organic synthesis as a building block for various compounds, meaning it can be used as a starting material to create other chemical compounds.

Use in pharmaceuticals

This chemical is also known for its use in the production of pharmaceuticals, meaning it can be used to create medications.

Potential use in new materials

2,3-Butadien-1-one, 1-(4-bromophenyl)has potential use in the development of new materials with desired properties, meaning it can be used to create new and improved materials.

Hazardous if not used and stored properly

It is important to handle this compound with care as it can be hazardous if not used and stored properly, meaning it can pose a risk to health or the environment if not handled correctly.

Upstream product

• 6048-21-1 4-bromobenzoyl cyanide 
• 106-96-7 propargyl bromide 
• 94612-95-0 1-(p-bromophenyl)-but-3-yn-1-ol 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 14297-34-8 2-(p-bromophenyl)furane 
• 56961-07-0 4'-bromo-3-methyl-1,1'-biphenyl 
• 52063-43-1 5-(4-bromophenyl)-3-methylisoxazole 
• 948293-34-3 3-methyl-5-p-bromophenyl-1-hydropyrazole 
• 1609633-98-8 ethyl 2-acetyl-5-(4-bromophenyl)-3-methylene-2,3-dihydrofuran-2-carboxylate 
• 1589561-86-3 ethyl 5-(2-(4-bromophenyl)-2-oxoethyl)-2-methylfuran-3-carboxylate 
• 1590402-68-8 (1-(4-bromobenzoyl)-2-methylindolizin-3-yl)(4-fluorophenyl)methanone 
• 1002255-62-0 7-(4-bromophenyl)-5-methyl-2-phenylpyrazolo[1,5-a]pyrimidine 
• 838267-69-9 7-(4-bromophenyl)-2,5-dimethylpyrazolo[1,5-a]pyrimidine 

Relevant articles and documents

Synthesis of vinylic sulfones in aqueous media

A green method for the sulfination of allenic carbonyl compounds to access a wide variety of vinylic sulfones is developed. This reaction works in aqueous media under very mild conditions. This reaction is atom economic. A wide variety of vinylic sulfones could be obtained in moderate to excellent yields with wide functional group tolerance. The efficiency of this method is demonstrated in some reactions where the desired products can be isolated by filtration.

A bicyclization reaction with two molecular allenyl ketones and isocyanides: Synthesis of a lactone-containing azaspirocycle derivative

A novel bicyclization reaction of two molecular allenyl ketones and isocyanides has been disclosed. This strategy allows for the construction of structurally complex spirocyclic lactam-lactone systems in an efficient manner. This protocol also demonstrate

Synthesis of 1,2-allenic ketones through oxidation of homopropargyl alcohols with CrO3(cat.)/TBHP under MWI

A CrO3 catalyzed oxidation of homopropargyl alcohols with tert-butyl hydroperoxide under microwave irradiation was found to be an efficient and rapid alternative for the preparation of 1,2-allenic ketones. The advantages of this procedure inclu