(S)-3,3'-Diiodo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene

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Reagent Code: #70488
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CAS Number 219583-87-6

science Other reagents with same CAS 219583-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 626.2 g/mol
Formula C₂₄H₂₀I₂O₄
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, agrochemicals, and fine chemicals by enabling the production of specific enantiomers with high purity. Its structure allows it to form stable complexes with transition metals, making it effective in asymmetric hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Additionally, it is employed in the synthesis of advanced materials and chiral catalysts, contributing to innovations in organic chemistry and industrial applications.

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inventory 100mg
10-20 days ฿567.00

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(S)-3,3'-Diiodo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, agrochemicals, and fine chemicals by enabling the production of specific enantiomers with high purity. Its structure allows it to form stable complexes with transition metals, making it effective in asymmetric hydrogenation, carbon-carbon bond formation, and other stereospecific transformatio

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, agrochemicals, and fine chemicals by enabling the production of specific enantiomers with high purity. Its structure allows it to form stable complexes with transition metals, making it effective in asymmetric hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Additionally, it is employed in the synthesis of advanced materials and chiral catalysts, contributing to innovations in organic chemistry and industrial applications.

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