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

98%

Reagent Code: #36522
fingerprint
CAS Number 2415751-83-4

science Other reagents with same CAS 2415751-83-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 442.5104 g/mol
Formula C₂₆H₃₆O₂P₂
badge Registry Numbers
MDL Number MFCD32201253
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst in asymmetric reactions. Its unique stereochemistry and structural rigidity make it highly effective in facilitating enantioselective transformations, particularly in the synthesis of complex organic molecules. It is often employed in catalytic systems for reactions such as hydrogenation, hydroformylation, and carbon-carbon bond formation, where high enantiomeric purity is required. Additionally, its application extends to the development of pharmaceuticals and fine chemicals, where precise control over stereochemistry is critical for achieving desired biological activity and product efficacy.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,876.00

Cart

No products

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

This chemical is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst in asymmetric reactions. Its unique stereochemistry and structural rigidity make it highly effective in facilitating enantioselective transformations, particularly in the synthesis of complex organic molecules. It is often employed in catalytic systems for reactions such as hydrogenation, hydroformylation, and carbon-carbon bond formation, where high enantiomeric purity is required. Additionally, its appl

This chemical is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst in asymmetric reactions. Its unique stereochemistry and structural rigidity make it highly effective in facilitating enantioselective transformations, particularly in the synthesis of complex organic molecules. It is often employed in catalytic systems for reactions such as hydrogenation, hydroformylation, and carbon-carbon bond formation, where high enantiomeric purity is required. Additionally, its application extends to the development of pharmaceuticals and fine chemicals, where precise control over stereochemistry is critical for achieving desired biological activity and product efficacy.

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...