1036373-39-3 | 1-Dicyclohexylphosphino-1′-{(R)-{(RP)-2-[(S)-1-(dimethylamino)ethyl]ferrocenyl}phenylphosphino}ferrocene

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	2 weeks	$658.00	$460.00

Description

• Catalog Number: AB58263
• Chemical Name: 1-Dicyclohexylphosphino-1′-{(R)-{(RP)-2-[(S)-1-(dimethylamino)ethyl]ferrocenyl}phenylphosphino}ferrocene
• CAS Number: 1036373-39-3
• Molecular Formula: C42H53Fe2NP2
• Molecular Weight: 745.5144
• MDL Number: MFCD18827475
• SMILES: [CH-]1C=CC=C1.C1CCC(CC1)P(C1=CC=C[CH-]1)C1CCCCC1.CN([C@H](C1=C[CH-]C=C1P(c1ccccc1)[C-]1C=CC=C1)C)C.[Fe+2].[Fe+2]

Upstream Synthesis Route

1-Dicyclohexylphosphino-1'-{(R)-{(RP)-2-[(S)-1-(dimethylamino)ethyl]ferrocenyl}phenylphosphino}ferrocene is a versatile ligand commonly used in chemical synthesis for asymmetric catalysis. This compound plays a crucial role in controlling the stereochemistry of various reactions by coordinating to metals and influencing the reaction pathways. Its unique structure, consisting of two ferrocene units and a chiral phosphine group, enables it to selectively bind to transition metals and facilitate enantioselective reactions.In asymmetric catalysis, this ligand is employed to promote a wide range of transformations, such as asymmetric hydrogenation, cross-coupling reactions, and cycloadditions. The chiral environment created by 1-Dicyclohexylphosphino-1'-{(R)-{(RP)-2-[(S)-1-(dimethylamino)ethyl]ferrocenyl}phenylphosphino}ferrocene allows for the production of chiral molecules with high optical purity, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, the modular design of this ligand allows for easy modification and fine-tuning of its properties, enabling chemists to tailor its structure for specific catalytic applications. Overall, 1-Dicyclohexylphosphino-1'-{(R)-{(RP)-2-[(S)-1-(dimethylamino)ethyl]ferrocenyl}phenylphosphino}ferrocene is a crucial component in the toolkit of organic chemists seeking to perform enantioselective reactions with high efficiency and selectivity.