(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 |
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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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