Pirralkonium bromide

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

(1,3-Dioxolan-2-ylmethyl)zinc bromide is an organozinc compound used as a reagent in Negishi cross-coupling reaction to prepare aryl or heteroaryl scaffolds via C-C bond formation. Application (1,3-Dioxolan-2-ylmethyl)zinc bromide can be used as a

Application Potent phase transfer organocatalyst for asymmetric &#945-alkylation of glycine derivatives at extremely low loadings. Features and Benefits Maruoka phase-transfer catalysts are: Operationally straightforward Environmentally friendly

Application Reactant involved in olefination of activated imines Modifier of PET nanocomposite fibers with functionalized multiwalled carbon nanotubes

Application Reactant for preparation of: Spirocyclohexadienones via Pd-catalyzed intramolecular ipso-Friedel-Crafts allylic alkylation Inhibitors of heat shock protein (Hsp90) as antitumor agents Carpanone-like molecules via an oxidative

(3-Bromopropyl)phosphonic acid

Application Reactant involved in: Synthesis of functionalized polyurethanes using cationic ring-opening polymerization and click chemistry Semipinacol rearrangement and direct arylation Olefination of benzaldehydes C-H activation /

Application Reactant for preparation of: Piperamide analogs as histone deacetylase (HDAC) inhibitors with antitumor activity Boron-containing benzoxaboroles as antimalarial agents Methyl alkenyl quinolones as antimycobacterial agents Solandelactone

Application Reactant for preparation of: Piperamide analogs as histone deacetylase (HDAC) inhibitors with antitumor activity Boron-containing benzoxaboroles as antimalarial agents Methyl alkenyl quinolones as antimycobacterial agents Solandelactone

Application Reactant involved in: Azidification C-H activation and &#946 -elimination to product an eight-membered ring system 1,3-Dipolar cycloaddition of azides onto alkenes Stereoselective SmI2-mediated coupling of unsaturated carbonyl

Application Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells Reactant for preparation of: Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions Methyl

Application Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells Reactant for preparation of: Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions Methyl