100965-18-2

Usage

Highly toxic

This substance is considered highly toxic, which means that even a small amount of exposure can cause harmful effects on human health, such as poisoning or severe organ damage.

Flammable

1-Propanone, 2,3-dibromo-1,3-bis(4-bromophenyl)can easily catch fire or explode when exposed to an ignition source, such as heat, sparks, or flames.

Use as an intermediate in the production of pharmaceuticals, dyes, and other chemical products

1-Propanone, 2,3-dibromo-1,3-bis(4-bromophenyl)- serves as a chemical building block or precursor in the synthesis of various pharmaceuticals, dyes, and other chemical products, making it valuable in the chemical industry.

Potential environmental hazard

Due to its toxic nature, 1-Propanone, 2,3-dibromo-1,3-bis(4-bromophenyl)can pose a threat to the environment, particularly soil and water sources, if not handled or disposed of properly.

Contamination of soil and water sources

The presence of this chemical in the environment can lead to the contamination of soil and water sources, which can have detrimental effects on the ecosystem and the organisms living within it.

Severe irritation to the skin, eyes, and respiratory system

Exposure to 1-Propanone, 2,3-dibromo-1,3-bis(4-bromophenyl)can cause significant irritation and damage to the skin, eyes, and respiratory system, highlighting the importance of proper handling and safety precautions.

Importance of handling with extreme caution and adhering to safety protocols

Due to its hazardous nature, it is crucial to handle 1-Propanone, 2,3-dibromo-1,3-bis(4-bromophenyl)with extreme care and follow established safety protocols to minimize the risk of accidents, exposure, and environmental contamination.

Upstream product

• 5471-96-5 (E)-1,3-bis(4-bromophenyl)prop-2-en-1-one 
• 5471-96-5 4,4'-dibromo-cis-chalcone 
• 99-90-1 para-bromoacetophenone 
• 1122-91-4 4-bromo-benzaldehyde 
• 5471-96-5 1,3-bis(4-bromophenyl)-2-propen-1-one 

Downstream Products

• 33170-68-2 1,3-bis-(4-bromo-phenyl)-propane-1,3-dione 
• 6909-81-5 1,3-bis(4-bromophenyl)-3-hydroxyprop-2-en-1-one 
• 914105-75-2 3-(3-bromophenyl)-5-(4-bromophenyl)isoxazole 
• 127019-14-1 4,6-Bis-(4-bromo-phenyl)-1,3-diaza-bicyclo[3.1.0]hex-3-ene 
• 117836-47-2 1,2-Bis-(4-bromo-phenyl)-1,1a-dihydro-3,7b-diaza-cyclopropa[a]naphthalene 
• 101422-91-7 4,4'-dibromo-β-methoxy-trans-chalcone 
• 101422-91-7 4,4'-dibromo-β-methoxy-cis-chalcone 

Relevant academic research and scientific papers

Theoretical and Experimental Study on Boron β-Diketonate Complexes with Intense Two-Photon-Induced Fluorescence in Solution and in the Solid State

Three boron diketonate chromophores with extended π-conjugated backbone were prepared and their spectroscopic features were investigated through a combined theoretical/experimental study. It was shown that these complexes, which undergo very large electro

Synthesis and in vitro antiprotozoal activities of dicationic 3,5-diphenylisoxazoles

3,5-Bis(4-amidinophenyl)isoxazole (3) - an analogue of 2,5-bis(4- amidinophenyl)furan (furamidine) in which the central furan ring is replaced by isoxazole - and 42 novel analogues were prepared by two general synthetic pathways. The 43 isoxazole derivati

Process for preparing vinyl substituted beta-diketones

A process for preparing vinyl substituted beta-diketones includes reacting a halogen-containing beta-diketone with an olefin in a reaction zone under Heck coupling reaction conditions in the presence of a catalyst, a base, and an organic phosphine to provide a vinyl substituted beta-diketone product.

Synthesis of vinyl-substituted β-diketones for polymerizable metal complexes

Polymerizable β-diketones for application to metal ion coordination have been prepared and characterized. Bromine-substituted β-diketones were synthesized under Claisen-Schmidt-type condensation conditions. Vinyl groups were substituted for the halide by