(R)-()-2-[2-(Diphenylphosphino)phenyl]-4-isopropyl-2-oxazoline

98%

  • Product Code: 113870
  Alias:    (R)-(+)-2-[2-(Diphenylphosphine)phenyl]-4-isopropylbisoxazole
  CAS:    164858-78-0
Molecular Weight: 373.43 g./mol Molecular Formula: C₂₄H₂₄NOP
EC Number: MDL Number: MFCD02684553
Melting Point: 85-90 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organometallic reactions. Its application is significant in the pharmaceutical industry, where it aids in the production of enantiomerically pure compounds, which are essential for developing drugs with specific biological activities. Additionally, it is employed in academic research to explore new catalytic processes and improve the efficiency of existing methods. Its unique structure allows for fine-tuning of catalytic systems, enhancing selectivity and yield in complex synthetic pathways.
Product Specification:
Test Specification
Melting Point 85-90
Purity (GC) 98-100%
Specific Rotation [A]20/D(C=1.4%, CHCL3) 45-51
Appearance White Crystalline Powder
Infrared Spectrometry Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days $83.63
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-
0.100 10-20 days $117.53
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0.250 10-20 days $264.44
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1.000 10-20 days $836.26
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(R)-()-2-[2-(Diphenylphosphino)phenyl]-4-isopropyl-2-oxazoline
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organometallic reactions. Its application is significant in the pharmaceutical industry, where it aids in the production of enantiomerically pure compounds, which are essential for developing drugs with specific biological activities. Additionally, it is employed in academic research to explore new catalytic processes and improve the efficiency of existing methods. Its unique structure allows for fine-tuning of catalytic systems, enhancing selectivity and yield in complex synthetic pathways.
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