N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(1R,2R)-2-[(11bR)-3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]-1,2-diphenylethyl]thiourea

97%

  • Product Code: 70753
  CAS:    1854082-48-6
Molecular Weight: 761.8200000000001 g./mol Molecular Formula: C₄₅H₃₃F₆N₃S
EC Number: MDL Number: MFCD32201228
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, protected from light, inert gas
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 complex organic molecules with high stereocontrol. Its application is significant in the pharmaceutical industry, where it aids in the production of enantiomerically pure drugs, ensuring enhanced efficacy and reduced side effects. Additionally, it is employed in academic research for developing novel synthetic methodologies and studying reaction mechanisms involving asymmetric induction. Its unique structure allows for effective hydrogen bonding interactions, making it a valuable tool in facilitating challenging transformations with high selectivity.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿6,192.00
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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(1R,2R)-2-[(11bR)-3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepin-4-yl]-1,2-diphenylethyl]thiourea
This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective reactions. It serves as a chiral thiourea catalyst, enabling the synthesis of complex organic molecules with high stereocontrol. Its application is significant in the pharmaceutical industry, where it aids in the production of enantiomerically pure drugs, ensuring enhanced efficacy and reduced side effects. Additionally, it is employed in academic research for developing novel synthetic methodologies and studying reaction mechanisms involving asymmetric induction. Its unique structure allows for effective hydrogen bonding interactions, making it a valuable tool in facilitating challenging transformations with high selectivity.
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