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

Short Description:

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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Product Detail

Product Tags

Description:

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 Properties:

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

Specifications:

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 & Storage:

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.

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.