(S)-3-(tert-Butyl)-4-(3,5-diisopropyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%

Reagent Code: #38409
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CAS Number 2444702-33-2

science Other reagents with same CAS 2444702-33-2

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scatter_plot Molecular Information
Weight 414.5174 g/mol
Formula C₂₅H₃₅O₃P
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MDL Number MFCD32641164
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in asymmetric catalysis, particularly in reactions where enantioselectivity is crucial. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where controlling the stereochemistry of the product is essential. Additionally, its sterically hindered and electron-rich aromatic system enhances its ability to stabilize transition states in catalytic cycles, improving reaction efficiency and selectivity.

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inventory 100mg
10-20 days ฿9,000.00

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(S)-3-(tert-Butyl)-4-(3,5-diisopropyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
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This chemical is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in asymmetric catalysis, particularly in reactions where enantioselectivity is crucial. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where controlling the stereochemistry of the product is essential. Additionally, its sterically hindered and electron-rich aromatic

This chemical is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in asymmetric catalysis, particularly in reactions where enantioselectivity is crucial. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where controlling the stereochemistry of the product is essential. Additionally, its sterically hindered and electron-rich aromatic system enhances its ability to stabilize transition states in catalytic cycles, improving reaction efficiency and selectivity.

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