349003

(1R)-(−)-(10-Camphorsulfonyl)oxaziridine

• Sinónimos: (1R)-(−)-(Camphorylsulfonyl)oxaziridine, (1R)-(−)-2,N-Epoxy-exo-10,2-bornanesultam
• Fórmula empírica (notación de Hill): C₁₀H₁₅NO₃S
• Número de CAS: 104372-31-8
• Peso molecular: 229.30
• Beilstein/REAXYS Number: 6274369
• MDL number: MFCD00075428
• UNSPSC Code: 12352005
• PubChem Substance ID: 24861490
• NACRES: NA.22

Propiedades

• form: powder
• optical activity: [α]20/D −44°, c = 2.2 in chloroform
• storage temp.: 2-8°C
• SMILES string: [H][C@@]12CC[C@@]3(CS(=O)(=O)N4OC34C1)C2(C)C
• InChI: 1S/C10H15NO3S/c1-8(2)7-3-4-9(8)6-15(12,13)11-10(9,5-7)14-11/h7H,3-6H2,1-2H3/t7-,9-,10?,11?/m1/s1
• InChI key: GBBJBUGPGFNISJ-JRNSMZEGSA-N

Descripción

Application

(1R)-(-)-(10-Camphorsulfonyl)oxaziridine may be used as an oxidant to prepare (S)-(-)-vasicinone via asymmetric oxidation of deoxyvasicinone.

Reactant involved in:

• Asymmetric synthesis of proton pump inhibitors
• Asymmetric synthesis of polyhydroxylated pyrrolidines
• Diastereoselective hydroxylation of chlorophylls a and b enolate anions

Used in impregnated silica nanoparticles for removal of sulfur mustard from wastewater

Used to modify blebbistatin for investigations of myosin inhibitor design

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable