Radiolabeled Custom Compounds

Application DuPhos and BPE Ligands: Highly Efficient Privileged Ligands 1,1&#8242-Bis[(2 R ,5 R )-2,5-diethylphospholano]ferrocene can be used: As a catalyst in the asymmetric hydrogenation reactions of olefins and ketones. As a component of a

Application 1,1,1,3,5,5,5-Heptamethyltrisiloxane can be used for the aromatic C-H silylation of arenes in the presence of a platinum complex catalyst. It can also be used as a reagent to synthesize: 3-Octyl-1,1,1,3,5,5,5-heptamethyltrisiloxane, an

Application 1,1,1,3,5,5,5-Heptamethyltrisiloxane can be used for the aromatic C-H silylation of arenes in the presence of a platinum complex catalyst. It can also be used as a reagent to synthesize: 3-Octyl-1,1,1,3,5,5,5-heptamethyltrisiloxane, an

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1,1,4,4-Tetraphenyl-1,3-butadiene

1，2，5，6-Tetrabromocyclooctane.

1,2-Diaminocyclohexane undergoes non-templated reaction with homochiral as well as the racemic form of trans -1,2-diaminocyclohexane with terephthaldehyde to yield (3+3)-cyclocondensed molecular triangles . It acts as ligand and forms organotin

1,2-Diaminocyclohexane undergoes non-templated reaction with homochiral as well as the racemic form of trans -1,2-diaminocyclohexane with terephthaldehyde to yield (3+3)-cyclocondensed molecular triangles . It acts as ligand and forms organotin

1,2-Diaminocyclohexane undergoes non-templated reaction with homochiral as well as the racemic form of trans -1,2-diaminocyclohexane with terephthaldehyde to yield (3+3)-cyclocondensed molecular triangles . It acts as ligand and forms organotin

1,2-Diaminocyclohexane undergoes non-templated reaction with homochiral as well as the racemic form of trans -1,2-diaminocyclohexane with terephthaldehyde to yield (3+3)-cyclocondensed molecular triangles . It acts as ligand and forms organotin

1，2-Dibromo-3，4，5，6-tetramethylbenzene.

1，2-Dibromo-3，4，5，6-tetramethylbenzene.