
Grupos Protectores
Los grupos protectores se utilizan en síntesis orgánica para enmascarar temporalmente grupos funcionales reactivos, permitiendo que ocurran reacciones selectivas sin interferencias. Estos grupos son esenciales para los procesos de síntesis en varias etapas, asegurando que partes específicas de la molécula permanezcan no reactivas mientras se realizan otras reacciones. En esta sección, encontrará una variedad de grupos protectores adecuados para diferentes grupos funcionales, junto con reactivos para su introducción y eliminación. En CymitQuimica, ofrecemos una gama completa de grupos protectores de alta calidad para facilitar sus estrategias sintéticas.
Subcategorías de "Grupos Protectores"
Productos de "Grupos Protectores"
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Acetamide, 2,2,2-trifluoro-N-methyl-N-(trimethylsilyl)-
CAS:Fórmula:C6H12F3NOSiPureza:97%Forma y color:LiquidPeso molecular:199.24628959999995Benzoic acid (trifluoromethanesulfonic acid)anhydride
CAS:Fórmula:C8H5F3O4SPureza:98%Forma y color:SolidPeso molecular:254.1831tert-Butyldiphenylsilyl Trifluoromethanesulfonate
CAS:Fórmula:C17H19F3O3SSiPureza:>98.0%(T)Forma y color:Colorless to Brown clear liquidPeso molecular:388.48N,N-Bis(trifluoromethylsulfonyl)aniline
CAS:Fórmula:C8H5F6NO4S2Pureza:98%Forma y color:SolidPeso molecular:357.25Di-tert-butyl Dicarbonate [Boc-reagent for Amino Acid]
CAS:Fórmula:C10H18O5Pureza:>95.0%(T)Forma y color:White or Colorless to Light yellow powder to lump to clear liquidPeso molecular:218.25Dimethylisopropylchlorosilane [Dimethylisopropylsilylating Agent]
CAS:Fórmula:C5H13ClSiPureza:>90.0%(GC)Forma y color:Colorless to Light orange to Yellow clear liquidPeso molecular:136.69Triphenylmethanesulfenyl Chloride
CAS:Fórmula:C19H15ClSPureza:>96.0%(T)(HPLC)Forma y color:Light orange to Yellow to Green powder to crystalPeso molecular:310.844-(Trimethylsilyl)Morpholine
CAS:Fórmula:C7H17NOSiPureza:97%Forma y color:LiquidPeso molecular:159.30152-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile
CAS:Fórmula:C13H14N2O3Pureza:>98.0%(N)Forma y color:White to Almost white powder to crystalPeso molecular:246.27N-(tert-Butoxycarbonyloxy)phthalimide
CAS:Fórmula:C13H13NO5Pureza:>95.0%(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular:263.25Cesium Fluoride
CAS:Fórmula:CsFPureza:min. 99.0 %Forma y color:White powder to crystalPeso molecular:151.90Benzoyl Chloride
CAS:Fórmula:C7H5ClOPureza:>98.0%(GC)(T)Forma y color:Colorless to Almost colorless clear liquidPeso molecular:140.571-(tert-Butyldimethylsilyl)imidazole [tert-Butyldimethylsilylating Agent]
CAS:Fórmula:C9H18N2SiPureza:>98.0%(T)Forma y color:Colorless to Almost colorless clear liquidPeso molecular:182.346-Bromo-7-hydroxy-4-(hydroxymethyl)coumarin
CAS:Fórmula:C10H7BrO4Pureza:>98.0%(T)Forma y color:White to Light yellow to Light orange powder to crystalPeso molecular:271.07Bromotriethylsilane
CAS:Fórmula:C6H15BrSiPureza:>96.0%(GC)Forma y color:White - Yellow LiquidPeso molecular:195.18p-Toluenesulfonyl Chloride
CAS:Fórmula:C7H7ClO2SPureza:>99.0%(GC)Forma y color:White to Light yellow powder to crystalPeso molecular:190.64Fmoc-glycinol
CAS:Fmoc-glycinol is a synthetase that is used to synthesize glycinol conjugates. It binds to the receptor on Gram-positive bacteria and blocks the synthesis of bacterial cell wall, leading to cell death. Fmoc-glycinol has been shown to have high binding constants with amines and an acyl chain, which allows it to bind with antigen. Fmoc-glycinol also has strong nucleophilic properties that allow it to react with chloride ions in water and other polar solvents. This reaction mechanism leads to the formation of a new bond between two molecules, which is called a glycinol linkage.Fórmula:C17H17NO3Pureza:Min. 95%Forma y color:White PowderPeso molecular:283.32 g/molSilane, chlorodimethyloctyl-
CAS:Fórmula:C10H23ClSiPureza:95%Forma y color:LiquidPeso molecular:206.82811999999998