diisopropyl((1S,2S)-2-aminocyclohexyl)phosphoramidate

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Reagent Code: #233693
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CAS Number 1792981-78-2

science Other reagents with same CAS 1792981-78-2

blur_circular Chemical Specifications

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Weight 278.33 g/mol
Formula C₁₂H₂₇N₂O₃P
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral ligand or catalyst precursor in asymmetric synthesis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its phosphoramidate structure with a defined stereochemistry enables high enantioselectivity in the production of chiral amines and alcohols, which are key intermediates in pharmaceuticals and fine chemicals. Commonly applied in transition metal-catalyzed reactions, especially with ruthenium or iridium complexes, to achieve efficient stereocontrol. Also explored in organocatalysis due to its ability to form hydrogen bonds and coordinate metals effectively.

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inventory 100mg
10-20 days ฿30,400.00

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diisopropyl((1S,2S)-2-aminocyclohexyl)phosphoramidate
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Used as a chiral ligand or catalyst precursor in asymmetric synthesis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its phosphoramidate structure with a defined stereochemistry enables high enantioselectivity in the production of chiral amines and alcohols, which are key intermediates in pharmaceuticals and fine chemicals. Commonly applied in transition metal-catalyzed reactions, especially with ruthenium or iridium complexes, to achieve efficient stereocontrol. Al

Used as a chiral ligand or catalyst precursor in asymmetric synthesis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its phosphoramidate structure with a defined stereochemistry enables high enantioselectivity in the production of chiral amines and alcohols, which are key intermediates in pharmaceuticals and fine chemicals. Commonly applied in transition metal-catalyzed reactions, especially with ruthenium or iridium complexes, to achieve efficient stereocontrol. Also explored in organocatalysis due to its ability to form hydrogen bonds and coordinate metals effectively.

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