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

97%,≥99% ee

Reagent Code: #96571
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CAS Number 2021202-03-7

science Other reagents with same CAS 2021202-03-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.41 g/mol
Formula C₂₁H₂₇O₃P
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

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 dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. These compounds are often intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its sterically hindered tert-butyl group and methoxy-substituted aromatic ring enhance its stability and selectivity in catalytic processes, making it a valuable tool for chemists aiming to achieve high enantiomeric purity in their products.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿3,591.00
100mg
10-20 days ฿8,811.00
500mg
10-20 days ฿35,991.00

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(S)-3-(tert-Butyl)-4-(2,6-dimethoxy-3,5-dimethylphenyl)-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 dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. These compounds are often intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its sterically hindered tert-butyl group

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 dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. These compounds are often intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its sterically hindered tert-butyl group and methoxy-substituted aromatic ring enhance its stability and selectivity in catalytic processes, making it a valuable tool for chemists aiming to achieve high enantiomeric purity in their products.

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