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 ProductionItem | 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 |
Description:
Specifications:
Package & Storage:
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 |
Advantages:
FAQ:
Application:
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.