[1-(2S,5S)-2,5-dimethylphospholanyl]-[2-(2S,5S)-2,5-dimethylphospholanyl-1-oxide]benzene

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Reagent Code: #53902
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CAS Number 1380079-15-1

science Other reagents with same CAS 1380079-15-1

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Weight 322.3600 g/mol
Formula C₁₈H₂₈OP₂
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MDL Number MFCD09750449
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This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring phosphorus atoms in a stereochemically defined environment, makes it highly effective in inducing enantioselectivity. It is often employed in hydrogenation, hydroformylation, and other carbon-carbon bond-forming reactions, where it helps produce chiral molecules with high enantiomeric purity. This is especially valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the stereochemistry of the product is critical for biological activity or desired properties. Additionally, its stability and tunable electronic properties make it a versatile tool in organometallic chemistry and catalyst design.

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inventory 100mg
10-20 days ฿3,492.00

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[1-(2S,5S)-2,5-dimethylphospholanyl]-[2-(2S,5S)-2,5-dimethylphospholanyl-1-oxide]benzene
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This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring phosphorus atoms in a stereochemically defined environment, makes it highly effective in inducing enantioselectivity. It is often employed in hydrogenation, hydroformylation, and other carbon-carbon bond-forming reactions, where it helps produce chiral molecules with high enantiomeric purity. This is especially valuable in the synthesis of p

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring phosphorus atoms in a stereochemically defined environment, makes it highly effective in inducing enantioselectivity. It is often employed in hydrogenation, hydroformylation, and other carbon-carbon bond-forming reactions, where it helps produce chiral molecules with high enantiomeric purity. This is especially valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the stereochemistry of the product is critical for biological activity or desired properties. Additionally, its stability and tunable electronic properties make it a versatile tool in organometallic chemistry and catalyst design.

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