104322-63-6 | (1S)-(+)-(10-Camphorsulfonyl)oxaziridine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$15.00	$11.00
10g	98%	in stock	$18.00	$13.00
25g	98%	in stock	$39.00	$28.00
100g	98%	in stock	$155.00	$109.00

Description

• Catalog Number: AB54668
• Chemical Name: (1S)-(+)-(10-Camphorsulfonyl)oxaziridine
• CAS Number: 104322-63-6
• Molecular Formula: C10H15NO3S
• Molecular Weight: 229.296
• MDL Number: MFCD21332910
• SMILES: O=S1(=O)C[C@@]23[C@]4(N1O4)C[C@H](C3(C)C)CC2

Computed Properties

• Complexity: 466
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 3
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• XLogP3: 1.5

Upstream Synthesis Route

(1S)-(+)-(10-Camphorsulfonyl)oxaziridine, also known as CSO, is a powerful oxidizing reagent commonly used in chemical synthesis. This chiral oxaziridine is highly versatile and plays a crucial role in various synthetic transformations due to its exceptional reactivity and selectivity.One of the key applications of (1S)-(+)-(10-Camphorsulfonyl)oxaziridine is its role as an enantioselective oxidizing agent. It is frequently employed in asymmetric oxidation reactions to convert various functional groups into their corresponding chiral products with high enantiomeric purity. The presence of the camphorsulfonyl moiety imparts significant stereocontrol during the oxidation process, making it a valuable tool in the synthesis of complex organic molecules.Furthermore, (1S)-(+)-(10-Camphorsulfonyl)oxaziridine is particularly useful in the oxidation of sulfides to sulfoxides and sulfones. This reaction proceeds efficiently under mild conditions and offers excellent control over the stereochemistry of the resulting products. Additionally, CSO can also be utilized in the oxidation of a wide range of functional groups, including alcohols, amines, and olefins, providing access to diverse synthetic pathways.Overall, the unique reactivity and stereochemical control offered by (1S)-(+)-(10-Camphorsulfonyl)oxaziridine make it a valuable reagent in asymmetric synthesis and organic chemistry, enabling the efficient construction of complex molecular structures with high levels of stereochemical purity.