(11AR)-()-10,11,12,13-TETRAHYDRODIINDENO[7,1-DE:1',7'-FG][1,3,2]DIOXAPHOSPHOCIN-5-BIS(R)-1PHENYLETHYL]AMINE

98%,ee99%

  • Product Code: 36153
  CAS:    500997-70-6
Molecular Weight: 505.59 g./mol Molecular Formula: C₃₃H₃₂NO₂P
EC Number: MDL Number: MFCD08459342
Melting Point: 99-101°C Boiling Point: 617.8±65.0 °C
Density: Storage Condition: -20℃
Product Description: This chemical is primarily utilized in the field of asymmetric synthesis and catalysis. Its unique structure, featuring a chiral phosphine ligand, makes it highly effective in facilitating enantioselective reactions, particularly in the synthesis of complex organic molecules. It is often employed in transition metal-catalyzed processes, such as hydrogenation, where it helps achieve high enantiomeric purity in the final products. This is particularly valuable in the pharmaceutical industry, where the production of single-enantiomer drugs is critical for efficacy and safety. Additionally, its application extends to the development of advanced materials and fine chemicals, where precise control over molecular chirality is essential.
Product Specification:
Test Specification
APPEARANCE White to brown solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days ฿1,300.00
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-
0.025 10-20 days ฿3,920.00
+
-
0.100 10-20 days ฿12,820.00
+
-
(11AR)-()-10,11,12,13-TETRAHYDRODIINDENO[7,1-DE:1',7'-FG][1,3,2]DIOXAPHOSPHOCIN-5-BIS(R)-1PHENYLETHYL]AMINE
This chemical is primarily utilized in the field of asymmetric synthesis and catalysis. Its unique structure, featuring a chiral phosphine ligand, makes it highly effective in facilitating enantioselective reactions, particularly in the synthesis of complex organic molecules. It is often employed in transition metal-catalyzed processes, such as hydrogenation, where it helps achieve high enantiomeric purity in the final products. This is particularly valuable in the pharmaceutical industry, where the production of single-enantiomer drugs is critical for efficacy and safety. Additionally, its application extends to the development of advanced materials and fine chemicals, where precise control over molecular chirality is essential.
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