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
| 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 |
| 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 |
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.
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.