(4S,​4'S)​-2,​2'-​Cyclopentylidenebis[​4,​5-​dihydro-​4-​phenyloxazole]

≥98%,99%e.e.

Reagent Code: #59744
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CAS Number 1639791-77-7

science Other reagents with same CAS 1639791-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 360.4 g/mol
Formula C₂₃H₂₄N₂O₂
thermostat Physical Properties
Boiling Point 511.8±50.0 °C
inventory_2 Storage & Handling
Density 1.25±0.1 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Its unique structure allows it to induce high stereoselectivity in transformations such as hydrogenation, cyclopropanation, and cross-coupling reactions. Additionally, it finds application in the development of advanced materials, where its chiral properties can influence the assembly and properties of molecular structures. Its versatility and efficiency make it a valuable tool in organic synthesis and material science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,192.00
inventory 100mg
10-20 days ฿2,547.00
inventory 1g
10-20 days ฿20,700.00

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(4S,​4'S)​-2,​2'-​Cyclopentylidenebis[​4,​5-​dihydro-​4-​phenyloxazole]
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This chemical is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Its unique structure allows it to induce high stereoselectivity in transformations such as hydrogenation, cyclopropanation, and cross-coupling reactions. Additionally, it finds application in the development of advan

This chemical is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Its unique structure allows it to induce high stereoselectivity in transformations such as hydrogenation, cyclopropanation, and cross-coupling reactions. Additionally, it finds application in the development of advanced materials, where its chiral properties can influence the assembly and properties of molecular structures. Its versatility and efficiency make it a valuable tool in organic synthesis and material science.

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