Grignard Reagents
Grignard reagents are vital in organic synthesis for the formation of carbon-carbon bonds. These organomagnesium compounds are key reagents in nucleophilic addition reactions, allowing for the synthesis of alcohols, ketones, and other organic molecules. At CymitQuimica, we provide a wide range of Grignard reagents to facilitate cutting-edge research in synthetic organic chemistry.
Found 77 products of "Grignard Reagents"
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(1,3-Dioxan-2-ylethyl)magnesium bromide, 0.5M 2-MeTHF
CAS:Formula:C11H21BrMgO3Purity:97.0%Color and Shape:Liquid, No data available.Molecular weight:305.495(5a,16b)-21-(Acetyloxy)-17-hydroxy-16-methylpregnane-3,20-dione
CAS:Controlled Product<p>Applications (5α,16β)-21-(Acetyloxy)-17-hydroxy-16-methylpregnane-3,20-dione is an intermediate used in the synthesis of (16β)-21-(Acetyloxy)-17-hydroxy-16-methylpregna-1,4-diene-3,20-dione (A187753), which is a useful intermediate that is used in the synthetic preparation of methylhydroxypregnendione via epoxidation, Grignard addition., and oxidation.<br>References Tian, W.; et al.: Faming Zhuanli Shenqing 18pp. Patent 2011 CODEN:CNXXEV<br></p>Formula:C24H36O5Color and Shape:NeatMolecular weight:404.54Di-sec-butylmagnesium - Lithium Chloride (13% in Tetrahydrofuran, ca. 0.8mol/L)
CAS:Formula:C8H18Mg·LiClColor and Shape:LiquidMolecular weight:180.93
