(R)-3-(tert-butyl)-4-(2,6-diphenoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%

Reagent Code: #55593
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CAS Number 1441830-74-5

science Other reagents with same CAS 1441830-74-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 454.4967 g/mol
Formula C₂₉H₂₇O₃P
badge Registry Numbers
MDL Number MFCD32641149
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phosphole core and bulky substituents, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where high enantioselectivity is required. Additionally, its stability and reactivity under various conditions make it a valuable tool in developing novel synthetic methodologies for creating optically active compounds.

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inventory 50mg
10-20 days ฿6,670.00

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(R)-3-(tert-butyl)-4-(2,6-diphenoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
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This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phosphole core and bulky substituents, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where high enantioselectivity is required. Additionally, its stability and reactivity under various conditions

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phosphole core and bulky substituents, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where high enantioselectivity is required. Additionally, its stability and reactivity under various conditions make it a valuable tool in developing novel synthetic methodologies for creating optically active compounds.

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