(S)​-5,​5',​6,​6',​7,​7',​8,​8'-​Octahydro-​3,​3'-​bis[4-​(trifluoromethyl)​phenyl]​-[1,​1'-​binaphthalene]​-​2,​2'-​diol

≥98%,99%e.e.

Reagent Code: #65640
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CAS Number 1228600-98-3

science Other reagents with same CAS 1228600-98-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 582.6 g/mol
Formula C₃₄H₂₈F₆O₂
thermostat Physical Properties
Melting Point 248 °C
Boiling Point 620.7±55.0 °C
inventory_2 Storage & Handling
Density 1.315±0.06 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the formation of carbon-carbon and carbon-heteroatom bonds, making it valuable in the production of pharmaceuticals and fine chemicals. Its robust structure and ability to induce chirality make it a key component in the synthesis of complex organic molecules, ensuring the desired stereochemistry in the final product. Additionally, it is used in the development of chiral catalysts for industrial processes, enhancing efficiency and selectivity in chemical transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,900.00
inventory 250mg
10-20 days ฿4,960.00

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(S)​-5,​5',​6,​6',​7,​7',​8,​8'-​Octahydro-​3,​3'-​bis[4-​(trifluoromethyl)​phenyl]​-[1,​1'-​binaphthalene]​-​2,​2'-​diol
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the formation of carbon-carbon and carbon-heteroatom bonds, making it valuable in the production of pharmaceuticals and fine chemicals. Its robust structure and ability to induce chirality make it a key component in the synthesis of complex organic molecules, ensuring the desired stereochemistry in the final product. Additio

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the formation of carbon-carbon and carbon-heteroatom bonds, making it valuable in the production of pharmaceuticals and fine chemicals. Its robust structure and ability to induce chirality make it a key component in the synthesis of complex organic molecules, ensuring the desired stereochemistry in the final product. Additionally, it is used in the development of chiral catalysts for industrial processes, enhancing efficiency and selectivity in chemical transformations.

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