CAS 1502-22-3
:Cyclohexenylcyclohexanone
Description:
Cyclohexenylcyclohexanone, with the CAS number 1502-22-3, is an organic compound characterized by its bicyclic structure, which includes both cyclohexene and cyclohexanone moieties. This compound typically appears as a colorless to pale yellow liquid and possesses a distinctive odor. It is known for its reactivity due to the presence of the double bond in the cyclohexene ring, making it susceptible to various chemical reactions such as electrophilic addition and oxidation. Cyclohexenylcyclohexanone is often utilized in organic synthesis and may serve as an intermediate in the production of more complex molecules. Its physical properties, such as boiling point and solubility, can vary depending on the specific conditions and purity of the sample. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Proper storage and handling protocols are essential to ensure safety in laboratory and industrial settings.
Formula:C12H18O
InChI:InChI=1S/C12H18O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h6,11H,1-5,7-9H2
InChI key:InChIKey=GVNVAWHJIKLAGL-UHFFFAOYSA-N
SMILES:O=C1C(C=2CCCCC2)CCCC1
Synonyms:- 1-(2-Oxocyclohexyl)cyclohexene
- 2-(1-cyclohexen-1-yl)-Cyclohexanone
- 2-(Cyclohex-1-en-1-yl)cyclohexan-1-one
- 2-(Cyclohex-1-enyl)cyclohexanone
- Cyclohexanone, 2-(1-cyclohexen-1-yl)-
- Cyclohexenylcyclohexanone
- NSC 518776
- CHCH
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Found 7 products.
2-(1-Cyclohexenyl)cyclohexanone
CAS:Formula:C12H18OPurity:>85.0%(GC)Color and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight:178.282-(1-Cyclohexenyl)cyclohexanone, 85+%, cont. ca 10% 2-cyclohexylidenecyclohexanone
CAS:<p>It is a perfuming agent. It is used for special solvents and as a raw material in agrochemicals and dyestuffs. 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 </p>Formula:C12H18OPurity:85+%Color and Shape:Liquid, Clear colorless to pale yellowMolecular weight:178.28Cyclohexanone, 2-(1-cyclohexen-1-yl)-
CAS:Formula:C12H18OPurity:98%Color and Shape:LiquidMolecular weight:178.27072-(1-Cyclohexenyl)Cyclohexanone
CAS:2-(1-Cyclohexenyl)CyclohexanonePurity:85%, cont. ca 10% 2-cyclohexylidenecyclohexanoneMolecular weight:178.28g/mol[1,1'-Bi(cyclohexan)]-1'-en-2-one
CAS:<p>[1,1'-Bi(cyclohexan)]-1'-en-2-one</p>Purity:95%Molecular weight:178.28g/mol2-(1-Cyclohexenyl)cyclohexanone
CAS:<p>2-(1-Cyclohexenyl)cyclohexanone (CCH) is a growth factor that belongs to the group of p2 class. It has been shown to inhibit the activity of thymidylate synthase, an enzyme that catalyzes the conversion of deoxyuridine 5'-triphosphate to thymidylate. CCH also inhibits cancer cell growth by inhibiting DNA synthesis and protein synthesis. The inhibition of this enzyme is thought to be due to its ability to form covalent bonds with amino groups on proteins, which prevents them from functioning as enzymes. CCH is synthesized in mitochondria and activated by hydrochloric acid, which converts it into a reactive species. This reactive species then reacts with unsaturated alkyl chains on fatty acids and reacts with aromatic hydrocarbons in the cell membrane, causing lipid peroxidation and cellular damage. The reaction mechanism for CCH involves ethylene diamine (ED) and</p>Formula:C12H18OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:178.27 g/mol2-(1-Cyclohexenyl)cyclohexanone
CAS:Formula:C12H18OPurity:98%Color and Shape:Liquid, No data available.Molecular weight:178.275





