Antipsychotics

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.

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.

Application Catalyst for: Intermolecular conjugate addition of alcohols to unsaturated ketones and esters Preparation of &#946-amino carbonyl compounds by N-heterocyclic carbene-catalyzed enantioselective Mannich reactions of

Application Catalyst for: Intermolecular conjugate addition of alcohols to unsaturated ketones and esters Preparation of &#946-amino carbonyl compounds by N-heterocyclic carbene-catalyzed enantioselective Mannich reactions of

Application This product is Informer compound X17 of the Aryl Halide Chemistry Informer Library developed by chemists at Merck &amp Co., Inc.

(S)-alpha,alpha-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol

Biochem/physiol Actions Metabolite of the mevalonate pathway, which plays a key role in the biosynthesis of sterols, dolichol, heme and ubiquinone. Of interest for research in the disease areas oncology, autoimmune diseases, artherosclerosis and

Biochem/physiol Actions Metabolite of the mevalonate pathway, which plays a key role in the biosynthesis of sterols, dolichol, heme and ubiquinone. Of interest for research in the disease areas oncology, autoimmune diseases, artherosclerosis and

Biochem/physiol Actions Metabolite of the mevalonate pathway, which plays a key role in the biosynthesis of sterols, dolichol, heme and ubiquinone. Of interest for research in the disease areas oncology, autoimmune diseases, artherosclerosis and

Biochem/physiol Actions Metabolite of the mevalonate pathway, which plays a key role in the biosynthesis of sterols, dolichol, heme and ubiquinone. Of interest for research in the disease areas oncology, autoimmune diseases, artherosclerosis and

Application Reactant for: Rhodium-catalyzed asymmetric hydrogenation reactions Wittig reaction Wittig methylenation Preparation of N -(phenylmethyl)- cis -pyrrolidinediacetic acid esters via double aza-Michael addition reaction Stereoselective

(Trifluoromethoxy)benzene is an aryl trifluoromethyl ether. (Trifluoromethoxy)benzene can be prepared from 4-chloro-1-(trifluoromethoxy)benzene via hydrogenolysis.