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Thermo Scientific Chemicals
D-Epoxone, 98%
CAS: 18422-53-2 | C12H18O6 | 258.27 g/mol
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Chemical Identifiers
CAS18422-53-2
IUPAC Name2,2,5',5'-tetramethyl-tetrahydro-2H-spiro[[1,3]dioxolo[4,5-c]pyran-6,2'-[1,4]dioxolan]-7-one
Molecular FormulaC12H18O6
InChI KeyIVWWFWFVSWOTLP-UHFFFAOYNA-N
SMILESCC1(C)OC2COC3(COC(C)(C)O3)C(=O)C2O1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Melting Point (clear melt)97-106°C
Optical Rotation-122.0 ± 1.5° (c=1 in chloroform)
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D-Epoxone is a chemical reagent used for enantioselective epoxidation of alkenes. It is involved in the synthesis of Irciniastatin (A and B), which are used as antitumor compounds. It is used as cytotoxic secondary metabolite.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
D-Epoxone is a chemical reagent used for enantioselective epoxidation of alkenes. It is involved in the synthesis of Irciniastatin (A and B), which are used as antitumor compounds. It is used as cytotoxic secondary metabolite.
Solubility
Soluble in chloroform and methanol.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
D-Epoxone is a chemical reagent used for enantioselective epoxidation of alkenes. It is involved in the synthesis of Irciniastatin (A and B), which are used as antitumor compounds. It is used as cytotoxic secondary metabolite.
Solubility
Soluble in chloroform and methanol.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Tran, A. T.; Luo, B.; Jagadeesh, Y.; Auberger, N.; Désiré, J.; Nakagawa, S.; Kato, A.; Zhang, Y.; Blériot, Y.; Sollogoub, M. Synthesis of pyrrolidine-based analogues of 2-acetamidosugars as N-acetyl-d-glucosaminidase inhibitors. Carbohydr. Res. 2015, 409, 56-62.
- Ren, X-D.; Zhao, N.; Xu, S.; Lü, H-N.; Ma, S-G.; Liu, Y-B.; Li, Y.; Qu, J.; Yu, S-S. Total synthesis of illicidione A and illihendione A. Tetrahedron 2015, 71 (29), 4821-4829.