Halometasone

Application 2-Bromoacetophenone has been used in the analysis of organic acids involving the formation of phenacyl derivatives .

2-Bromoacetophenone is a commonly used derivatization agent for fatty acid detection in biological samples. Application Preparation of crystalline esters from acids Legal Information LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Legal Information ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Legal Information ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

3'-Iodoacetophenone

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

4&#8242-Bromoacetophenone is used as an organic building block in Heck and Suzuki coupling reactions. Generates phenyl radicals upon UV irradiation.

4&#8242-Bromoacetophenone is used as an organic building block in Heck and Suzuki coupling reactions. Generates phenyl radicals upon UV irradiation.

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Melting range (lower value): &#8805 49 &#176C Melting range (upper value): &#8804 52 &#176C Identity (IR): passes test

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Melting range (lower value): &#8805 49 &#176C Melting range (upper value): &#8804 52 &#176C Identity (IR): passes test

Application Reactant for: Preparation of cyclopentene fused benzofurans and indoles via Pd-catalyzed tandem ring opening-ring closing reaction with diazabicyclic alkenes Highly regioselective synthesis of spirocyclic compounds by a

Pd(0)-catalyzed cross coupling reaction of 4&#8242-iodoacetophenone with siloxane has been reported. Heck-Mizoroki reactions of 4&#8242-iodoacetophenone with styrene catalyzed by Pd nanoparticles in the flow reactor has been reported.