40396-54-1

Basic information

• Product Name: Ethanedione, (3-bromophenyl)phenyl-
• CAS NO: 40396-54-1
• Molecular Formula: C14H9BrO2
• Molecular Weight: 289.128
• Mol File: 40396-54-1.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: Ethanedione, (3-bromophenyl)phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanedione, (3-bromophenyl)phenyl-(40396-54-1)
• EPA Substance Registry System: Ethanedione, (3-bromophenyl)phenyl-(40396-54-1)

Safety Data

• Hazardous Substances Data: 40396-54-1(Hazardous Substances Data)

Usage

General Description

Ethanedione, (3-bromophenyl)phenyl-, also known as 3-bromobenzoylacetylacetone, is a chemical compound with the molecular formula C14H11BrO2. It is a derivative of acetylacetone and is commonly used as a chelating ligand in coordination chemistry. Ethanedione, (3-bromophenyl)phenyl- is known for its ability to form stable complexes with metal ions, making it useful in various chemical and biological applications. It is also used as a reagent in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals. Additionally, it has been studied for its potential anti-cancer and anti-inflammatory properties. Overall, ethanedione, (3-bromophenyl)phenyl- is a versatile compound with a wide range of uses in the field of chemistry and beyond.

Upstream product

• 93-98-1 N-phenyl benzoyl amide 
• 38430-03-4 N-phenylbenzimidoyl chloride 
• 1392015-27-8 (Z)-1-(3-bromophenyl)-2-phenyl-2-(phenylimino)ethan-1-one 
• 29778-29-8 1-phenyl-2-(m-bromo)phenylacetylene 
• 536-74-3 phenylacetylene 
• 591-18-4 1-Bromo-3-iodobenzene 
• 1878-67-7 3-Bromophenylacetic acid 
• 98288-51-8 2-(3-bromophenyl)acetyl chloride 
• 27798-44-3 2-(3-bromophenyl)-1-phenylethan-1-one 
• 14064-45-0 (E)-3-bromostilbene 
• 1617534-60-7 1-(3-bromophenyl)-2-oxo-2-phenylethyl benzoate 
• 2142-63-4 1-(3-Bromophenyl)ethanone 
• 100-42-5 styrene 
• 40887-80-7 3-bromophenylhydrazine 

Downstream Products

• 40396-55-2 3-bromo-α,α,α',α'-tetrafluorobibenzyl 
• 856875-79-1 2-imino-3-methyl-5-phenyl-5-[3-(pyridin-3-yl)phenyl]imidazolidin-4-one 
• 856875-78-0 C₂₁H₁₈N₄O 
• 1370656-78-2 C₂₀H₁₇N₅O 
• 887911-14-0 C₂₂H₂₀N₄O 
• 887911-20-8 C₂₂H₁₇N₅O 
• 887911-80-0 C₂₁H₁₇FN₄O 
• 856875-77-9 C₂₂H₁₉N₃O 
• 887911-21-9 (R)-2-imino-5-(3'-methoxy-[1,1'-biphenyl]-3-yl)-3-methyl-5-phenyl-imidazolidin-4-one 
• 856885-13-7 C₂₃H₂₁N₃O₂ 
• 856885-29-5 C₂₄H₂₃N₃O₂ 
• 1049655-77-7 C₂₁H₁₈N₄O 
• 856875-46-2 5-(3-bromophenyl)-2-imino-3-methyl-5-phenylimidazolidin-4-one 
• 1370656-79-3 C₂₃H₂₁N₃O₂ 

Relevant articles and documents

Conversion of alkynes into 1,2-diketones using HFIP as sacrificial hydrogen donor and DMSO as dihydroxylating agent

A metal-free and hypervalent iodine free conversion of internal alkynes into 1,2-diketo compounds has been described. The efficacy of the present protocol rely on the use of HFIP (1,1,1,3,3,3-Hexafluoro-2-propanol) as reducing agent of alkynes and DMSO as dihydroxylating agent of olefins to acquire the desired chemical transformations. The obtained 1,2-diketones were further transformed into useful derivatives.

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