(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-4,4'-diphenyl-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole

97%,>99% ee

Reagent Code: #59681
fingerprint
CAS Number 1202033-21-3

science Other reagents with same CAS 1202033-21-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 538.6 g/mol
Formula C₃₄H₃₆O₂P₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, filled with inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, agrochemicals, and fine chemicals by enabling the production of enantiomerically pure compounds. Its unique structure allows it to effectively coordinate with transition metals, enhancing the efficiency and selectivity of catalytic processes such as hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions. Additionally, it is employed in the synthesis of complex organic molecules, contributing to advancements in medicinal chemistry and material science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,820.00
inventory 100mg
10-20 days ฿15,030.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-4,4'-diphenyl-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, agrochemicals, and fine chemicals by enabling the production of enantiomerically pure compounds. Its unique structure allows it to effectively coordinate with transition metals, enhancing the efficiency and selectivity of catalytic processes such as hydrogenation, hydroformylation, and ca

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, agrochemicals, and fine chemicals by enabling the production of enantiomerically pure compounds. Its unique structure allows it to effectively coordinate with transition metals, enhancing the efficiency and selectivity of catalytic processes such as hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions. Additionally, it is employed in the synthesis of complex organic molecules, contributing to advancements in medicinal chemistry and material science.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...