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

97%

Reagent Code: #68676
fingerprint
CAS Number 1807740-34-6

science Other reagents with same CAS 1807740-34-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 370.42 g/mol
Formula C₂₅H₂₃OP
badge Registry Numbers
MDL Number MFCD31630706
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in organic synthesis as a chiral ligand or catalyst, particularly in asymmetric reactions to produce enantiomerically pure compounds. Its anthracene moiety allows for fluorescence-based detection or monitoring in catalytic processes. The tert-butyl group enhances steric hindrance, improving selectivity in transformations like hydrogenation or cross-coupling reactions. It is also employed in the development of advanced materials, such as chiral polymers or frameworks, for applications in optoelectronics or sensing technologies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,879.00
inventory 250mg
10-20 days ฿9,225.00
inventory 1g
10-20 days ฿23,778.00

Cart

No products

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

Used in organic synthesis as a chiral ligand or catalyst, particularly in asymmetric reactions to produce enantiomerically pure compounds. Its anthracene moiety allows for fluorescence-based detection or monitoring in catalytic processes. The tert-butyl group enhances steric hindrance, improving selectivity in transformations like hydrogenation or cross-coupling reactions. It is also employed in the development of advanced materials, such as chiral polymers or frameworks, for applications in optoelectron

Used in organic synthesis as a chiral ligand or catalyst, particularly in asymmetric reactions to produce enantiomerically pure compounds. Its anthracene moiety allows for fluorescence-based detection or monitoring in catalytic processes. The tert-butyl group enhances steric hindrance, improving selectivity in transformations like hydrogenation or cross-coupling reactions. It is also employed in the development of advanced materials, such as chiral polymers or frameworks, for applications in optoelectronics or sensing technologies.

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...