(S)-1-(3-(Tert-butyl)-2,3-dihydrobenzo[d][1,3]oxaphosphol-4-yl)-2,5-diphenyl-1H-pyrrole

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Reagent Code: #37891
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CAS Number 1683581-58-9

science Other reagents with same CAS 1683581-58-9

blur_circular Chemical Specifications

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Weight 411.4752 g/mol
Formula C₂₇H₂₆NOP
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MDL Number MFCD31707610
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phospholane core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. It is often employed in hydrogenation, hydroformylation, or other catalytic processes where high stereocontrol is required. Additionally, its stability and selectivity make it a valuable tool in the development of novel synthetic methodologies for complex molecule construction.

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inventory 100mg
10-20 days ฿11,690.00

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(S)-1-(3-(Tert-butyl)-2,3-dihydrobenzo[d][1,3]oxaphosphol-4-yl)-2,5-diphenyl-1H-pyrrole
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phospholane core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. It is often employed in hydrogenation, hydroformylation, or other catalytic processes where high stereocontrol is required. Additionally, its stabilit

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phospholane core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. It is often employed in hydrogenation, hydroformylation, or other catalytic processes where high stereocontrol is required. Additionally, its stability and selectivity make it a valuable tool in the development of novel synthetic methodologies for complex molecule construction.

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