()-6,6'-[(1R,3R)-1,3-Dimethyl-1,3-propanediyl]bis(oxy)bis[4,8-bis(t-butyl)-2,10-dimethoxy-bibenzo[d,f][1,3,2]dioxaphosphepin]

98%

Reagent Code: #68581
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CAS Number 149646-83-3

science Other reagents with same CAS 149646-83-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 876.99 g/mol
Formula C₄₉H₆₆O₁₀P₂
badge Registry Numbers
MDL Number MFCD06798296
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in reactions where high enantioselectivity is required. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where the precise control of stereochemistry is crucial. The compound’s unique structure allows it to effectively coordinate with metal centers, enhancing the selectivity and efficiency of catalytic processes such as hydrogenation, cross-coupling, and carbon-carbon bond formation. Its application is especially valuable in producing enantiomerically pure compounds, which are essential in drug development and other high-precision chemical industries.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿6,228.00
inventory 250mg
10-20 days ฿15,858.00
inventory 1g
10-20 days ฿41,220.00
inventory 5g
10-20 days ฿122,400.00

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()-6,6'-[(1R,3R)-1,3-Dimethyl-1,3-propanediyl]bis(oxy)bis[4,8-bis(t-butyl)-2,10-dimethoxy-bibenzo[d,f][1,3,2]dioxaphosphepin]
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in reactions where high enantioselectivity is required. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where the precise control of stereochemistry is crucial. The compound’s unique structure allows it to effectively coordinate with metal centers, enhancing the selectivity and efficiency of catalytic processes such as hydrogenation, cross-coupling, and carbon-carbon bond formation. I

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in reactions where high enantioselectivity is required. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where the precise control of stereochemistry is crucial. The compound’s unique structure allows it to effectively coordinate with metal centers, enhancing the selectivity and efficiency of catalytic processes such as hydrogenation, cross-coupling, and carbon-carbon bond formation. Its application is especially valuable in producing enantiomerically pure compounds, which are essential in drug development and other high-precision chemical industries.

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