(S)-BTBBPh-SaBOX

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Reagent Code: #59721
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CAS Number 1428328-51-1

science Other reagents with same CAS 1428328-51-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 598.8200000000001 g/mol
Formula C₄₁H₄₆N₂O₂
badge Registry Numbers
MDL Number MFCD26404519
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

(S)-BTBBPh-SaBOX is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its application is significant in the pharmaceutical industry for the production of enantiomerically pure compounds, which are crucial for drug development. The compound is also employed in organic synthesis to facilitate reactions such as asymmetric hydrogenation, carbon-carbon bond formation, and other transformations that require high stereochemical control. Additionally, it finds use in academic research for studying mechanistic pathways and developing new catalytic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,041.00

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(S)-BTBBPh-SaBOX
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(S)-BTBBPh-SaBOX is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its application is significant in the pharmaceutical industry for the production of enantiomerically pure compounds, which are crucial for drug development. The compound is also employed in organic synthesis to facilitate reactions such as asymmetric hydrogenation, carbon-carbon bond formation, and other transformations that require high stereochemical control. A

(S)-BTBBPh-SaBOX is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its application is significant in the pharmaceutical industry for the production of enantiomerically pure compounds, which are crucial for drug development. The compound is also employed in organic synthesis to facilitate reactions such as asymmetric hydrogenation, carbon-carbon bond formation, and other transformations that require high stereochemical control. Additionally, it finds use in academic research for studying mechanistic pathways and developing new catalytic processes.

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