(1S)-(+)-(10-Camphorsulfonyl)oxaziridine
(1S)-(+)-(10-Camphorsulfonyl)oxaziridine (CAS: 104322-63-6, C10H15NO3S) is a chiral oxaziridine reagent supplied by Tech Serve Solutions. With a molecular weight of 229.30, this compound is primarily utilized in asymmetric synthesis for stereoselective oxidation reactions. It is essential for researchers and chemists involved in creating enantiomerically pure compounds, particularly in pharmaceutical and fine chemical synthesis where precise stereochemistry is critical.
- IUPAC
- (1S)-(+)-(Camphorylsulfonyl)oxaziridine,(1S)-(+)-2,N-Epoxy-exo-10,2-bornanesultam
Asymmetric Synthesis
This chiral oxaziridine serves as a key reagent in asymmetric synthesis, enabling the stereoselective introduction of oxygen functionalities into various organic molecules. Its ability to perform enantioselective oxidations makes it valuable for producing chiral intermediates.
Chiral Catalyst and Reagent
As a chiral catalyst and reagent, (1S)-(+)-(10-Camphorsulfonyl)oxaziridine is instrumental in achieving high stereocontrol in synthetic transformations. It is employed in enantioselective oxidations, such as asymmetric epoxidation and hydroxylation reactions.
Hydroxylation Reactions
The compound is frequently used for asymmetric hydroxylation of enolates and other nucleophiles. This process is crucial for the synthesis of chiral alcohols and other oxygenated compounds with defined stereochemistry.
Pharmaceutical Intermediate Synthesis
In the pharmaceutical industry, precise stereochemistry is paramount. This reagent aids in the synthesis of complex chiral molecules and active pharmaceutical ingredients (APIs) where specific enantiomers are required for therapeutic efficacy.
| Molecular weight | 229.30 |
|---|---|
| Empirical formula | C10H15NO3S |
| Optical activity | [α]28/D +45°, c = 2 in chloroform |
| Storage temperature | 2-8°C |
| Impurities tested | <1% toluene |
| Melting point | 172-174 °C(lit.) |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is (1S)-(+)-(10-Camphorsulfonyl)oxaziridine used for?
+
(1S)-(+)-(10-Camphorsulfonyl)oxaziridine is primarily used as a chiral reagent in asymmetric synthesis for stereoselective oxidation reactions, including hydroxylation, to produce enantiomerically pure compounds.
What is the CAS number and formula for (1S)-(+)-(10-Camphorsulfonyl)oxaziridine?
+
The CAS number is 104322-63-6 and the empirical formula is C10H15NO3S.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies this product with an impurity level of <1% toluene. We do not represent this product as USP, BP, EP, or any other pharmacopoeia grade.
How should (1S)-(+)-(10-Camphorsulfonyl)oxaziridine be handled and stored?
+
Handle with appropriate personal protective equipment, including eyeshields and gloves. Use a type N95 (US) or type P1 (EN143) respirator filter if needed. Store at 2-8°C. Refer to the Safety Data Sheet for comprehensive safety information.
How is (1S)-(+)-(10-Camphorsulfonyl)oxaziridine packed and exported?
+
This chemical is packed and exported in compliance with all relevant transport regulations. Please contact us for specific packaging and export details for your region.
How can I request a sample or quote for (1S)-(+)-(10-Camphorsulfonyl)oxaziridine?
+
To request a sample or quote, please use the 'Request a Quote' or 'Sample Request' forms on our website, or contact our sales team directly with your requirements.
▶ Related products
1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis
1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis