(S)-DTBM-SEGPHOS

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Reagent Code: #68687
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CAS Number 210169-40-7

science Other reagents with same CAS 210169-40-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1179.54 g/mol
Formula C₇₄H₁₀₀O₈P₂
badge Registry Numbers
MDL Number MFCD09753003
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(S)-DTBM-SEGPHOS is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity. This ligand is also employed in asymmetric carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitution, enabling the synthesis of complex chiral intermediates for pharmaceuticals and agrochemicals. Its robust steric and electronic properties make it a preferred choice for achieving high enantioselectivity in various synthetic transformations. Additionally, (S)-DTBM-SEGPHOS is utilized in the production of fine chemicals and active pharmaceutical ingredients (APIs), where precise control over stereochemistry is critical. Its application extends to academic research and industrial processes, contributing to advancements in asymmetric synthesis.

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Test Parameter Specification
Melting point 126-128
Optical Purity (EE) 97.5-100
Purity 98-100%
Appearance White to light yellow to light orange powder to crystal
Infrared Spectrum Conforms to Structure
Specific rotation [α]_D^{20} (c=1, CHCl3) 52-56

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,280.00
inventory 500mg
10-20 days ฿7,920.00
inventory 1g
10-20 days ฿13,490.00

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(S)-DTBM-SEGPHOS
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(S)-DTBM-SEGPHOS is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity. This ligand is also employed in asymmetric carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitution, enabling the synthesis of complex chiral intermediates for pharmaceuticals and agrochemicals. Its robust steric and electroni

(S)-DTBM-SEGPHOS is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity. This ligand is also employed in asymmetric carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitution, enabling the synthesis of complex chiral intermediates for pharmaceuticals and agrochemicals. Its robust steric and electronic properties make it a preferred choice for achieving high enantioselectivity in various synthetic transformations. Additionally, (S)-DTBM-SEGPHOS is utilized in the production of fine chemicals and active pharmaceutical ingredients (APIs), where precise control over stereochemistry is critical. Its application extends to academic research and industrial processes, contributing to advancements in asymmetric synthesis.

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