(1R,2R)-N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-1,2-DIPHENYLETHANE-1,2-DIAMINE

98%

  • Product Code: 71242
  CAS:    852212-90-9
Molecular Weight: 394.53 g./mol Molecular Formula: C₂₃H₂₆N₂O₂S
EC Number: MDL Number: MFCD11501122
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, away from light
Product Description: This compound is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in organic reactions. Its unique structure enables the induction of chirality, making it valuable in the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, epoxidation, and other stereoselective transformations, enhancing the efficiency and selectivity of these processes. Additionally, it finds application in the development of novel catalytic systems for academic research and industrial processes, contributing to advancements in synthetic chemistry.
Product Specification:
Test Specification
APPEARANCE Light yellow to yellow Solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿830.00
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-
0.250 10-20 days ฿2,370.00
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-
1.000 10-20 days ฿6,050.00
+
-
(1R,2R)-N-(2,4,6-TRIMETHYLPHENYLSULFONYL)-1,2-DIPHENYLETHANE-1,2-DIAMINE
This compound is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in organic reactions. Its unique structure enables the induction of chirality, making it valuable in the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, epoxidation, and other stereoselective transformations, enhancing the efficiency and selectivity of these processes. Additionally, it finds application in the development of novel catalytic systems for academic research and industrial processes, contributing to advancements in synthetic chemistry.
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