* Solvent bondable with typically used solvents in the industry like
cyclohexanone (CH), THF or MEK.
All the synthesized polyurethanes were soluble in many of the common aprotic solvents, such as
cyclohexanone, DMF, DMAc, DMSO, and NMP, indicating that polyurethanes offer good processability and thus, optical quality thin films could be easily prepared from their solutions.
Cyclohexanone is an oily liquid that is mainly used in industrial chemical production for the organic synthesis of adipic acid, caprolactam, polyvinyl chloride and its copolymers, and methacrylate ester polymers (OECD, 1996).
For particleboard finished with acrylic water-based paint, the ethanediol, 1,2-propylene glycol, aromatic hydrocarbons, methylbenzene, xylene, and
cyclohexanone should be controlled.
Cyclohexanone can be harmful if inhaled, phenol is known to be acutely toxic and to presumably have mutagenic potential and isophorone is a category 2 carcinogen, which means that this is a suspect substance in the development of cancer in humans, Medical Xpress reported.
Commonly, different kinds of methods are known for the large scale production of
cyclohexanone by the conversion of cyclohexanol [7, 8].
Synthesis of polymers (PTpC and PCzC) and polymer-QDs nanocomposites (PTpC-QDs and PCzC-QDs):
Cyclohexanone, 4,4'-diformyltriphenylamine, 9-(2-ethylhexyl)carbazole-3,6-dicarboxaldehyde, sodium hydroxide, ethanol, and QDs (CdSeS@ZnS for red, CdZnSeS@ZnS for green, and CdZnS@ZnS for blue) were used to synthesize PTpC, PCzC, PTpC-QDs, and PCzC-QDs.
Compound (2E, 6E)-2,6-bis (2-(trifluoromethyl) benzylidene)
cyclohexanone (C66) is a synthetic derivative of natural active curcumin.
Hyperplasia of the urinary bladder transitional epithelium was observed in mice exposed to MEKO but not with a similar chemical,
cyclohexanone oxime.
First, the effects of APAP on responses to the prooxidant irritant acrolein and the nonoxidant irritant
cyclohexanone were examined to confirm whether any effects of APAP were oxidant-specific rather than generalized in nature.
It details conditions of typical syntheses, limitations of their applicability, and the possibility of vinyl chloride or dichloroethane application instead of acetylene; chemical engineering aspects of the first synthesis of tetrahydroindole and indole from commercially available oxime of
cyclohexanone and acetylene; new facets of pyrroles and N-vinyl pyrroles reactivity in the reactions with the participation of the pyrrole ring and N-vinyl groups; and about 1,000 structures of novel pyrrole compounds and their yields and physical-chemical characteristics.
