(1R)-(−)-(10-Camphorsulfonyl)oxaziridine

98%

  • Product Code: 70847
  Alias:    (1R)-(-)-Camphorsulfonazine (1R)-(-)-2,N-epoxy-exo-10, 2-bornane sultam (2S,8aR)-(-)-Camphorsulfonazine (1R)-(-)-10-Camphorsulfonazine (-)-Camphorsulfonazine
  CAS:    104372-31-8
Molecular Weight: 229.29 g./mol Molecular Formula: C₁₀H₁₅NO₃S
EC Number: MDL Number: MFCD00075428
Melting Point: 170-174 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: (1R)-(−)-(10-Camphorsulfonyl)oxaziridine is widely used as a chiral oxidizing agent in organic synthesis. It is particularly effective in the enantioselective oxidation of sulfides to sulfoxides, a reaction crucial in the production of chiral pharmaceuticals. The compound's ability to transfer oxygen selectively makes it valuable in asymmetric synthesis, where it helps create optically active molecules with high enantiomeric purity. Additionally, it is employed in the synthesis of complex natural products and fine chemicals, where precise control over stereochemistry is essential. Its stability and reactivity under mild conditions further enhance its utility in laboratory and industrial applications.
Product Specification:
Test Specification
APPEARANCE white crystalline powder
INFRARED SPECTRUM Conforms to Structure
PURITY 97.5 100%
SOLUBILITY Colorless and clear(2.5%, CH2Cl2)
Specific rotation a20DC1 Acetone -47
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿610.00
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-
5.000 10-20 days ฿1,780.00
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-
25.000 10-20 days ฿6,800.00
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-
(1R)-(−)-(10-Camphorsulfonyl)oxaziridine
(1R)-(−)-(10-Camphorsulfonyl)oxaziridine is widely used as a chiral oxidizing agent in organic synthesis. It is particularly effective in the enantioselective oxidation of sulfides to sulfoxides, a reaction crucial in the production of chiral pharmaceuticals. The compound's ability to transfer oxygen selectively makes it valuable in asymmetric synthesis, where it helps create optically active molecules with high enantiomeric purity. Additionally, it is employed in the synthesis of complex natural products and fine chemicals, where precise control over stereochemistry is essential. Its stability and reactivity under mild conditions further enhance its utility in laboratory and industrial applications.
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