Clodronate or clodronic acid

Application 3-Phosphonopropionic acid was used to functionalize the bulk phosphate glass surface .

Application Reactant involved in: Radical coupling Synthesis of organosoluble zirconium phosphonate nanocomposites Click-chemistry Asymmetric epoxidation of unfunctionalized olefins Negishi alkyl-aryl cross-coupling Synthesis of hydrolytically

Application Reactant involved in: Radical coupling Synthesis of organosoluble zirconium phosphonate nanocomposites Click-chemistry Asymmetric epoxidation of unfunctionalized olefins Negishi alkyl-aryl cross-coupling Synthesis of hydrolytically

Application Acts as a nucleophile for nucleophilic addition reactions for synthesis of allene epoxides Reactant for: Stereoselectivity studies of the Staudinger reaction Enantioselective formation of diols via epoxidation and hydration reactions

Application Acts as a nucleophile for nucleophilic addition reactions for synthesis of allene epoxides Reactant for: Stereoselectivity studies of the Staudinger reaction Enantioselective formation of diols via epoxidation and hydration reactions

Biochem/physiol Actions Potent antagonist at metabotropic glutamic acid receptors.

Phosphonoacetic acid inhibits specifically human cytomegalovirus DNA synthesis in virus-infected human fibroblasts . It also inhibits the synthesis of herpes simplex virus DNA in infected cells and the activity of the virus-specific DNA polymerase

Phosphonoacetic acid inhibits specifically human cytomegalovirus DNA synthesis in virus-infected human fibroblasts . It also inhibits the synthesis of herpes simplex virus DNA in infected cells and the activity of the virus-specific DNA polymerase

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034 . This CRM is traceable to primary material from an NMI, e.