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

97%

Reagent Code: #36523
fingerprint
CAS Number 2207601-10-1

science Other reagents with same CAS 2207601-10-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 414.4572 g/mol
Formula C₂₄H₃₂O₂P₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where stereoselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its unique structure and stereochemistry enable it to induce high enantioselectivity, making it valuable for creating complex molecules with specific chiral centers. Additionally, it may be used in the development of advanced materials and fine chemicals where precise control over molecular architecture is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,983.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-dimethyl-2,2',3,3'-tetrahydro-4,4'-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 stereoselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its unique structure and stereochemistry enable it to induce high enantioselectivity, making it valuable for creat

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where stereoselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its unique structure and stereochemistry enable it to induce high enantioselectivity, making it valuable for creating complex molecules with specific chiral centers. Additionally, it may be used in the development of advanced materials and fine chemicals where precise control over molecular architecture is required.

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...