(1S)-(+)-(10-Camphorsulfonyl)oxaziridine CAS 104322-63-6 Purity ≥98.5% (HPLC) High Purity

Name: (1S)-(+)-(10-Camphorsulfonyl)oxaziridine Synonyms: (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine CAS: 104322-63-6 Appearance: Off-White or Pale Yellow Crystalline Powder Purity: ≥98.5% (HPLC) Chiral Compounds, Commercial Production

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Chemical Properties:

Package: Bottle, Aluminium foil bag, Cardboard Drum, 25kg/Drum, or according to customer's requirement. Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.Manufacturer Supply with High Purity and Stable Quality (1S)-(+)-(10-Camphorsulfonyl)oxaziridine CAS 104322-63-6 (1R)-(-)-(10-Camphorsulfonyl)oxaziridine CAS 104372-31-8 Chiral Compounds, High Quality, Commercial Production
Item Specifications
Appearance Off-White or Pale Yellow Crystalline Powder
Purity  ≥98.5% (HPLC)
Melting Point 168.0~172.0℃
Specific Rotation [a]D20 +43.0° ~ +47.0° (C=2.3, In CHCl3)
Loss on Drying ≤1.0%
Residue on Ignition ≤0.30%
Heavy Metals (Pb) ≤20ppm
Test Standard Enterprise Standard
Usage Chiral Compounds; Pharmaceutical Intermediates

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Chemical Name (1S)-(+)-(10-Camphorsulfonyl)oxaziridine
Synonyms (1S)-(+)-(Camphorylsulfonyl)oxaziridine; (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine
CAS Number 104322-63-6 
CAT Number RF-CC267
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C10H15NO3S
Molecular Weight 229.3
Shipping Condition Shipped Under Ambient Temperature
Brand Ruifu Chemical

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Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (1S)-(+)-(10-Camphorsulfonyl)oxaziridine (CAS: 104322-63-6) with high quality. (1S)-(+)-(10-Camphorsulfonyl)oxaziridine (CAS: 104322-63-6) is a useful Camphor derivative, a useful synthetic intermediate. Used for asymmetric hydroxylation. (1S)-(+)-(10-Camphorsulfonyl)oxaziridine (CAS: 104322-63-6) can be used: To convert prochiral ketone enolates into optically active α-hydroxy ketones via enantioselective asymmetric oxidation. In the synthesis of thymidine oligonucleotides connected through pyrophosphates. In the asymmetric synthesis of proton pump inhibitors like (R)-Rabeprazole sodium and (R)-Lansoprazole sodium from the corresponding DBU salt of prochiral sulfide. In the preparation of phosphonoacetate and thiophosphonoacetate oligodeoxynucleotides by oxidizing the corresponding phosphinoacetate.

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