(11aS)-5-oxide-3,7-bis(3,5-diMethylphenyl)-10,11,12,13-tetrahydro-5-hydroxy-Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin

98%

Reagent Code: #65664
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CAS Number 1412439-82-7

science Other reagents with same CAS 1412439-82-7

blur_circular Chemical Specifications

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Weight 522.6 g/mol
Formula C₃₃H₃₁O₄P
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This specialty chemical is a chiral phosphorus ligand with a unique (11aS)-configured diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin core, featuring 3,5-dimethylphenyl substituents at positions 3 and 7, a 5-oxide, and 5-hydroxy group. It is primarily used in asymmetric catalysis as a ligand for copper-catalyzed enantioselective conjugate additions of organozinc reagents to α,β-unsaturated carbonyls and other Michael acceptors, delivering high enantioselectivities. This niche application supports the synthesis of chiral intermediates for pharmaceuticals and fine chemicals.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿7,920.00
inventory 50mg
10-20 days ฿32,040.00

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(11aS)-5-oxide-3,7-bis(3,5-diMethylphenyl)-10,11,12,13-tetrahydro-5-hydroxy-Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin
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This specialty chemical is a chiral phosphorus ligand with a unique (11aS)-configured diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin core, featuring 3,5-dimethylphenyl substituents at positions 3 and 7, a 5-oxide, and 5-hydroxy group. It is primarily used in asymmetric catalysis as a ligand for copper-catalyzed enantioselective conjugate additions of organozinc reagents to α,β-unsaturated carbonyls and other Michael acceptors, delivering high enantioselectivities. This niche application supports the syn

This specialty chemical is a chiral phosphorus ligand with a unique (11aS)-configured diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin core, featuring 3,5-dimethylphenyl substituents at positions 3 and 7, a 5-oxide, and 5-hydroxy group. It is primarily used in asymmetric catalysis as a ligand for copper-catalyzed enantioselective conjugate additions of organozinc reagents to α,β-unsaturated carbonyls and other Michael acceptors, delivering high enantioselectivities. This niche application supports the synthesis of chiral intermediates for pharmaceuticals and fine chemicals.

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