14153-75-4

Usage

Physical properties

yellow to light brown crystalline powder

Common uses

organic synthesis, pharmaceutical research

Functional groups

aromatic and aldehyde
Versatile building block for organic synthesis
Unique reactivity due to bromophenyl group
Wide range of chemical transformations due to oxopropanal moiety

Upstream product

• 99-90-1 para-bromoacetophenone 
• 109-94-4 formic acid ethyl ester 

Downstream Products

• 77953-48-1 1,3,3-Trimethyl-2-<3-(p-bromobenzoyl)-2-propen-1-ylidene>indoline 
• 118947-84-5 6-(4-Brom-phenyl)-2-thioxo-1,2-dihydro-pyridin-3-carbonitril 
• 4203-30-9 1-(4-bromo-phenyl)-2-diazo-ethanone 
• 570391-40-1 3-(4-Bromo-phenyl)-2-diazo-3-oxo-propionaldehyde 
• 99-90-1 para-bromoacetophenone 
• 7064-31-5 5-(4-Bromophenyl)isoxazole 
• 128918-20-7 3-Amino-6-(4-brom-phenyl)-thieno<2,3-b>pyridin-2-carbonsaeuredimethylamid 
• 128917-94-2 6-(4-Brom-phenyl)-2-dimethylaminocarbonylmethylthio-pyridin-3-carbonitril 
• 128918-21-8 3-Amino-6-(4-bromo-phenyl)-thieno[2,3-b]pyridine-2-carboxylic acid diethylamide 
• 1187371-80-7 2-[2-(4-bromophenyl)-2-oxoethyl]-1,3,4-thiazidin-5-one 
• 1187371-89-6 2-[2-(4-bromophenyl)-2-oxoethyl]-3,4-dihydro-1,3,4-benzothiadiazepin-5(2H)-one 
• 943425-33-0 3-(4-bromophenyl)-3-oxopropanal semicarbazone 
• 1155720-99-2 3-(4-bromophenyl)-3-oxopropanal oxime-ethyl ether 
• 1155721-00-8 3-(4-bromophenyl)-3-oxopropanal dioxime-ethyl ether 

Relevant academic research and scientific papers

Design, synthesis and biological evaluation of 3-(4-halophenyl)-3- oxopropanal and their derivatives as novel antibacterial agents

In continuing our program aimed to search for potent drugs for bacterial infections, a series of 3-(4-halophenyl)-3-oxopropanal and their derivatives were designed, synthesized and their antibacterial activities in vitro against both Gram-positive bacteri

Identification and optimisation of 5-amino-7-aryldihydro-1,4-diazepines as 5-HT2A ligands

A several series of low molecular weight 5-HT2A leads were identified from an analysis of HTS data, the exploration of SAR and optimization of one series using parallel synthesis are described, affording compound 22 (5-HT2A IC50 1.1 nM).