(2R,3R)-3-(tert-Butyl)-4-(2,6-dimethoxyphenyl)-2-isopropyl-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%

Reagent Code: #36472
fingerprint
CAS Number 1477517-19-3

science Other reagents with same CAS 1477517-19-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.4300 g/mol
Formula C₂₂H₂₉O₃P
badge Registry Numbers
MDL Number MFCD32206570
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. The presence of the tert-butyl and isopropyl groups enhances steric control, improving selectivity in producing chiral molecules. This compound is valuable in pharmaceutical research for synthesizing enantiomerically pure drugs, where chirality plays a critical role in biological activity. Additionally, it may find use in material science for developing chiral polymers or advanced catalytic systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,122.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2R,3R)-3-(tert-Butyl)-4-(2,6-dimethoxyphenyl)-2-isopropyl-2,3-dihydrobenzo[d][1,3]oxaphosphole
No image available

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. The presence of the tert-butyl and isopropyl groups enhances steric control, improving selectivity in producing chiral molecules. This compound is valuable in pharm

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. The presence of the tert-butyl and isopropyl groups enhances steric control, improving selectivity in producing chiral molecules. This compound is valuable in pharmaceutical research for synthesizing enantiomerically pure drugs, where chirality plays a critical role in biological activity. Additionally, it may find use in material science for developing chiral polymers or advanced catalytic systems.

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...