Antiviral drugs

1-Phenylpyrazole undergoes cyclometallation with rhodium trichloride to yield rac -di(&#956-chloro) tetrakis [2-(pyrazol-1-yl)phenyl- C 1 , N 2 &#8242]dirhodium . The activation of the C-H bond of 1-phenylpyrazole autocatalyzed by the co-product

1-Phenylpyrazole has been used: · in the preparation of 4,5-diphenylpyrazolo[1,5-a]quinoline, 1-(1,2,3,4-tetraphenylnaphthalen-5-yl)pyrazole and 1-(1,2,3,4,5,6,7,8-octaphenylanthracen-9-yl)pyrazole · as cyclometallated ligand in the preparation of

1-Phenylpyrazole has been used: · in the preparation of 4,5-diphenylpyrazolo[1,5-a]quinoline, 1-(1,2,3,4-tetraphenylnaphthalen-5-yl)pyrazole and 1-(1,2,3,4,5,6,7,8-octaphenylanthracen-9-yl)pyrazole · as cyclometallated ligand in the preparation of

1-Phenylpyrazole has been used: · in the preparation of 4,5-diphenylpyrazolo[1,5-a]quinoline, 1-(1,2,3,4-tetraphenylnaphthalen-5-yl)pyrazole and 1-(1,2,3,4,5,6,7,8-octaphenylanthracen-9-yl)pyrazole · as cyclometallated ligand in the preparation of

1-Phenylpyrazole has been used: · in the preparation of 4,5-diphenylpyrazolo[1,5-a]quinoline, 1-(1,2,3,4-tetraphenylnaphthalen-5-yl)pyrazole and 1-(1,2,3,4,5,6,7,8-octaphenylanthracen-9-yl)pyrazole · as cyclometallated ligand in the preparation of

1-Phenylpyrazole has been used: · in the preparation of 4,5-diphenylpyrazolo[1,5-a]quinoline, 1-(1,2,3,4-tetraphenylnaphthalen-5-yl)pyrazole and 1-(1,2,3,4,5,6,7,8-octaphenylanthracen-9-yl)pyrazole · as cyclometallated ligand in the preparation of

CAS No.: 503417-37-6 Molecular Formula: C8H10N2·HCl Molecular Weight: 170.68 MDL No.: MFCD08059320 Storage Temperature: Store at 0-8°C

Synonyms: (2-Pyridylmethyl)piperazine Purity Limit: &ge 95% (HPLC) CAS No.: 298705-64-3 Molecular Formula: C10H15N3 Molecular Weight: 177.

1-PYRROLIDINEVALERONITRILE-1G

1-Triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methoxy-methyl-amide.

Application Reactant for: Cascade reactions of enals for enantioselective synthesis of indane derivatives Enantioselective conjugate addition for synthesis of &#945-branched indoles Synthesis of 1,2-dioxanes with antitrypanosomal activity

Suitable for molecular immunology, molecular biology and nucleic acid methodologies, when applicable. This product is a concentrated stock solution and should be diluted appropriately with distilled, deionized water or equivalent to its final