(2S,3S)-4-(anthracen-9-yl)-3-(tert-butyl)-2-methyl-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%

Reagent Code: #36542
fingerprint
CAS Number 1884594-02-8

science Other reagents with same CAS 1884594-02-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.4499 g/mol
Formula C₂₆H₂₅OP
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring an anthracene group and a phosphole ring, allows it to effectively induce chirality in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where enantioselectivity is crucial for achieving the desired biological activity or properties. Additionally, its stability and steric properties make it suitable for use in challenging catalytic transformations, such as cross-coupling reactions or hydrogenation processes. The compound’s ability to control stereochemistry makes it valuable in the development of optically active compounds, which are essential in drug discovery and material science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,937.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2S,3S)-4-(anthracen-9-yl)-3-(tert-butyl)-2-methyl-2,3-dihydrobenzo[d][1,3]oxaphosphole
No image available

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring an anthracene group and a phosphole ring, allows it to effectively induce chirality in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where enantioselectivity is crucial for achieving the desired biological activity or properties. Additionally, its stability and steric p

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring an anthracene group and a phosphole ring, allows it to effectively induce chirality in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where enantioselectivity is crucial for achieving the desired biological activity or properties. Additionally, its stability and steric properties make it suitable for use in challenging catalytic transformations, such as cross-coupling reactions or hydrogenation processes. The compound’s ability to control stereochemistry makes it valuable in the development of optically active compounds, which are essential in drug discovery 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...