Controlled substance analgesic amides and amines

Cochranes atom centers for Orbit molecular models

DescriptionCatalyst for one-pot diazo transfer-click reactionsA heterogeneous catalyst, primarily reported to mediate a tandem diazo transfer-click reaction starting from the corresponding amine rather than the azide. This catalyst system has been

CU AMINE ARYLATION MICRO V2

Application A ready-to-use reagent used to couple amine ligands to aldehyde functional groups. The coupling buffer reaction is a reductive amination of the intermediate Schiff&#8242s base to a stable C&#8722N bond.

Application A ready-to-use reagent used to couple amine ligands to aldehyde functional groups. The coupling buffer reaction is a reductive amination of the intermediate Schiff&#8242s base to a stable C&#8722N bond.

CYCLOHEXANECARBOXYLIC ACID (4-NITRO-PHENYL)-AMIDE-

D-Aspartic acid alpha-amide.

D-Aspartic acid alpha-amide.

di-adamantylalkylphosphine is a bulky and electron-rich phosphine ligand that is highly effective for palladium catalyzed cross-coupling reactions such as Heck and Suzuki coupling, Buchwald-Hartwig amination of aryl chlorides, and α-arylation

di-adamantylalkylphosphine is a bulky and electron-rich phosphine ligand that is highly effective for palladium catalyzed cross-coupling reactions such as Heck and Suzuki coupling, Buchwald-Hartwig amination of aryl chlorides, and α-arylation

Product description：Dichlorobis(tri-o-tolylphosphine)palladium(II) is a useful catalyst for C-C and C-N coupling reactions.Application：Catalyst for C-C and C-N coupling reaction.Dichlorobis(tri-o-tolylphosphine)palladium(II) has been employed as

Dichlorobis(tri- o -tolylphosphine)palladium(II) is a useful catalyst for C-C and C-N coupling reactions. Application Application Guide for Palladium Catalyzed Cross-Coupling Reactions Catalyst for C-C and C-N coupling reaction.