(R)-1-[(R)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenylethyldi-tert-butylphosphine

98%

Reagent Code: #68646
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CAS Number 187733-50-2

science Other reagents with same CAS 187733-50-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 658.61 g/mol
Formula C₃₈H₅₂FeO₂P₂
badge Registry Numbers
MDL Number MFCD08561156
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. Its unique structure, featuring a ferrocene backbone and phosphine groups, allows it to effectively induce chirality in catalytic reactions, such as hydrogenation, cross-coupling, and carbon-carbon bond formation. The presence of tert-butyl and methoxy-dimethylphenyl groups enhances its steric and electronic properties, making it highly selective and efficient in producing enantiomerically pure compounds. It is especially valuable in the production of chiral intermediates for drugs, agrochemicals, and other bioactive molecules, where high enantioselectivity is critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,350.00
inventory 250mg
10-20 days ฿5,157.00
inventory 100mg
10-20 days ฿2,439.00

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(R)-1-[(R)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenylethyldi-tert-butylphosphine
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. Its unique structure, featuring a ferrocene backbone and phosphine groups, allows it to effectively induce chirality in catalytic reactions, such as hydrogenation, cross-coupling, and carbon-carbon bond formation. The presence of tert-butyl and methoxy-dimethylphenyl groups enhances its steric and electronic properties, making it highly selective and efficie

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. Its unique structure, featuring a ferrocene backbone and phosphine groups, allows it to effectively induce chirality in catalytic reactions, such as hydrogenation, cross-coupling, and carbon-carbon bond formation. The presence of tert-butyl and methoxy-dimethylphenyl groups enhances its steric and electronic properties, making it highly selective and efficient in producing enantiomerically pure compounds. It is especially valuable in the production of chiral intermediates for drugs, agrochemicals, and other bioactive molecules, where high enantioselectivity is critical.

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