
CAS 1020174-04-2: 1-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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1-Methylpyrazole-3-boronic acid pinacol ester
CAS:1-Methylpyrazole-3-boronic acid pinacol esterPurity:0.97Molecular weight:208.07g/mol1-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
CAS:Controlled ProductFormula:C10H17BN2O2Color and Shape:NeatMolecular weight:208.0651-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-d3
CAS:Controlled ProductFormula:C10D3H14BN2O2Color and Shape:NeatMolecular weight:211.0841H-Pyrazole, 1-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS:Formula:C10H17BN2O2Purity:98%Color and Shape:SolidMolecular weight:208.06521-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole
CAS:1-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-pyrazole is a reagent in organic synthesis. It is an intermediate in the synthesis of pinacol esters and isomers thereof. 1-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h pyrazole can be prepared by diazotization with sodium nitrite and hydrochloric acid followed by heating in an alcoholic solution of pinacol. The synthetic method for this compound has been described.br>br> The target product of this chemical reaction is pinacol ester. Pinacol esters are used as intermediates for the synthesis of many other compounds including pharmaceuticals and fragrances. Diazotization with sodium nitrite and hydrochlorFormula:C10H17BN2O2Purity:Min. 95%Molecular weight:208.07 g/mol1-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:208.07000732421875