4-(11bS)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-ylmorpholine

97%

  • Product Code: 70646
  CAS:    185449-81-4
Molecular Weight: 401.4 g./mol Molecular Formula: C₂₄H₂₀NO₃P
EC Number: MDL Number:
Melting Point: 233-239°C Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This chemical is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its unique structure, featuring a dinaphtho-dioxaphosphepine core, makes it highly effective in asymmetric catalysis, particularly in reactions where enantioselectivity is critical. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where the precise control of stereochemistry is essential. Additionally, it finds application in the development of advanced materials, where its ability to induce chirality can influence the properties of polymers or other functional materials. Its role in facilitating stereocontrolled transformations makes it a valuable tool in both academic research and industrial processes.
Product Specification:
Test Specification
APPEARANCE White to off-white Solid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿2,440.00
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4-(11bS)-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-ylmorpholine
This chemical is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its unique structure, featuring a dinaphtho-dioxaphosphepine core, makes it highly effective in asymmetric catalysis, particularly in reactions where enantioselectivity is critical. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where the precise control of stereochemistry is essential. Additionally, it finds application in the development of advanced materials, where its ability to induce chirality can influence the properties of polymers or other functional materials. Its role in facilitating stereocontrolled transformations makes it a valuable tool in both academic research and industrial processes.
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