Search Thermo Fisher Scientific
Cyclohexanone
Cyclohexanone is a toxic, flammable, organic, cyclic, six-carbon molecule with a ketone functional group. Applications for the compound include use in the production of nylon, as a chemical reaction medium, and as a solvent.
Products (4)
Learn More (5)
Documents & Support
(482)4 Products
Filter
Cyclohexanone, 99+%, Thermo Scientific Chemicals Thermo Scientific Chemicals
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
Cyclohexanone, ACS, 99+%, Thermo Scientific Chemicals Thermo Scientific Chemicals
Cyclohexanone is used as an industrial solvent and paint remover. It acts as a precursor to nylon 6,6 and nylon 6 and cyclohexanone oxime, which gives caprolactam on rearrangement. Further, it is used as a chemical reaction medium, adhesives, sealants and agricultural products.
Cyclohexanone Oxime 97%, Thermo Scientific Chemicals Thermo Scientific Chemicals
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
Cyclohexanone, 99.8%, extra pure, Thermo Scientific Chemicals Thermo Scientific Chemicals
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
Learn More (5)
View all
The allylic rearrangement of tri-O-acetyl-D-glucal to the corresponding 2,3-unsaturated hemiacetal when heated under aqueous conditions was first reported in 1914 by German chemist Emil Fischer. However, it was the British chemist Robert Ferrier, who in the 1960s ultimately realized the synthetic...
Named after the German chemist Ernst Otto Beckmann, the Beckmann rearrangement involves the conversion of aldoximes and ketoximes to their corresponding amides under acidic conditions. The reaction is usually carried out under under termperatures greater than 130°C, and in the presence of a large...