(1R,2R)-N,N'-Di-p-tosyl-1,2-cyclohexanediamine

≥98%,≥99% e.e.

  • Product Code: 70792
  CAS:    143585-47-1
Molecular Weight: 422.6 g./mol Molecular Formula: C₂₀H₂₆N₂O₄S₂
EC Number: MDL Number:
Melting Point: 170-173°C Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: (1R,2R)-N,N'-Di-p-tosyl-1,2-cyclohexanediamine is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, enabling the production of enantiomerically pure compounds. This chemical is also employed in the synthesis of complex organic molecules, aiding in the creation of intermediates for drug discovery and development. Its application extends to the field of material science, where it is used in the preparation of chiral materials with specific optical properties. Additionally, it serves as a valuable tool in academic research for studying stereochemistry and reaction mechanisms.
Product Specification:
Test Specification
APPEARANCE White to off-white Solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿400.00
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-
1.000 10-20 days ฿1,820.00
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-
5.000 10-20 days ฿4,140.00
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-
(1R,2R)-N,N'-Di-p-tosyl-1,2-cyclohexanediamine
(1R,2R)-N,N'-Di-p-tosyl-1,2-cyclohexanediamine is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the development of pharmaceuticals, enabling the production of enantiomerically pure compounds. This chemical is also employed in the synthesis of complex organic molecules, aiding in the creation of intermediates for drug discovery and development. Its application extends to the field of material science, where it is used in the preparation of chiral materials with specific optical properties. Additionally, it serves as a valuable tool in academic research for studying stereochemistry and reaction mechanisms.
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