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Thermo Scientific Chemicals
Cyclobutanone, 98%, stab. with ca 0.1% BHT
CAS: 1191-95-3 | C4H6O | 70.09 g/mol
化学物質識別子
CAS1191-95-3
仕様
スペックシート
スペックシートAppearance (Color)Clear or slightly turbid, colorless to pale yellow
FormLiquid
Assay (GC)>97.5%
Refractive Index1.4190-1.4230 @ 20?C
Cyclobutanone is used in preparation of cyclobutane derivatives. It is used as a starting material for aminocyclobutanecarboxylic acid through sulfonyloxiranes. It is also used to prepare dihydro-furan-2-one in presence of polystyrene-bound phenylselenic acid as catalyst. Further, it is involved in the photochemical synthesis of nucleoside analogues such as bicyclic nucleosides and isonucleosides.
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
Cyclobutanone is used in preparation of cyclobutane derivatives. It is used as a starting material for aminocyclobutanecarboxylic acid through sulfonyloxiranes. It is also used to prepare dihydro-furan-2-one in presence of polystyrene-bound phenylselenic acid as catalyst. Further, it is involved in the photochemical synthesis of nucleoside analogues such as bicyclic nucleosides and isonucleosides.
Solubility
Immiscible with water.
Notes
Store in a cool place. Incompatible with strong oxidizing agents, strong bases and strong reducing agents.
Cyclobutanone is used in preparation of cyclobutane derivatives. It is used as a starting material for aminocyclobutanecarboxylic acid through sulfonyloxiranes. It is also used to prepare dihydro-furan-2-one in presence of polystyrene-bound phenylselenic acid as catalyst. Further, it is involved in the photochemical synthesis of nucleoside analogues such as bicyclic nucleosides and isonucleosides.
Solubility
Immiscible with water.
Notes
Store in a cool place. Incompatible with strong oxidizing agents, strong bases and strong reducing agents.
RUO – Research Use Only
General References:
- Lumbroso, A.; Catak, S.; Sulzer-Mosse, S.; Mesmaeker, A. D. Efficient access to functionalized cyclobutanone derivatives using cyclobuteniminium salts as highly reactive Michael acceptors. Tetrahedron Lett. 2015, 56 (19), 2397-2401.
- Souillart, L.; Cramer, N. Regiodivergent Cyclobutanone Cleavage: Switching Selectivity with Different Lewis Acids. Chem. Eur. J. 2015, 21 (5), 1863-1867.