N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(9R)-6'-methoxycinchonan-9-yl]thiourea

≥98%,99%d.e.

  • Product Code: 57519
  CAS:    852913-25-8
Molecular Weight: 594.6 g./mol Molecular Formula: C₂₉H₂₈F₆N₄OS
EC Number: MDL Number:
Melting Point: 150°C Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the synthesis of optically active compounds with high selectivity. Its application is significant in pharmaceutical synthesis, where it aids in producing chiral intermediates for drugs. Additionally, it is employed in organic synthesis to facilitate transformations such as Michael additions, Mannich reactions, and other carbon-carbon bond-forming processes. Its unique structure, featuring trifluoromethyl groups and a cinchona alkaloid derivative, enhances its catalytic efficiency and stereocontrol, making it valuable in the development of complex organic molecules.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.025 10-20 days ฿4,446.00
+
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0.100 10-20 days ฿9,297.00
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-
0.500 10-20 days ฿30,150.00
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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(9R)-6'-methoxycinchonan-9-yl]thiourea
This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the synthesis of optically active compounds with high selectivity. Its application is significant in pharmaceutical synthesis, where it aids in producing chiral intermediates for drugs. Additionally, it is employed in organic synthesis to facilitate transformations such as Michael additions, Mannich reactions, and other carbon-carbon bond-forming processes. Its unique structure, featuring trifluoromethyl groups and a cinchona alkaloid derivative, enhances its catalytic efficiency and stereocontrol, making it valuable in the development of complex organic molecules.
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