Description

4-(trans-4-Methylcyclohexyl)cyclohexanone (CAS No. 151772-66-6) is a high-purity cyclohexanone derivative with the molecular formula C₁₃H₂₂O. This bicyclic ketone features a trans-configuration at the 4-methylcyclohexyl substituent, ensuring superior stereochemical consistency for advanced synthetic applications. With a molecular weight of 194.32 g/mol, this compound exhibits excellent stability and solubility in common organic solvents, making it ideal for pharmaceutical intermediates, liquid crystal materials, and fragrance synthesis. Rigorously tested via GC, HPLC, and NMR to confirm ≥98% purity, our product meets the stringent requirements of research and industrial laboratories. Available in scalable quantities with custom packaging options, it is supplied with comprehensive analytical documentation, including COA and MSDS.

Properties

• CAS Number: 151772-66-6
• Complexity: 191
• IUPAC Name: 4-(4-methylcyclohexyl)cyclohexanone
• InChI: InChI=1S/C13H22O/c1-10-2-4-11(5-3-10)12-6-8-13(14)9-7-12/h10-12H,2-9H2,1H3
• InChI Key: RHUNWKYRWMYYMP-UHFFFAOYSA-N
• Exact Mass: 194.167065321
• Molecular Formula: C13H22O
• Molecular Weight: 194.31
• SMILES: CC1CCC(CC1)C2CCC(=O)CC2
• Topological: 17.1
• Monoisotopic Mass: 194.167065321
• Synonyms: 151772-66-6, trans-4′-Methyl[1,1′-bicyclohexyl]-4-one, 4-(trans-4-methylcyclohexyl)cyclohexanone, 4-(4-methylcyclohexyl)cyclohexan-1-one, 914221-47-9, trans-4′-Methyl-[1,1′-bi(cyclohexan)]-4-one, Trans-4-(Trans-4-methylcyclohexyl)cyclohexylanone, (1’R,4’R)-4′-METHYL-[1,1′-BI(CYCLOHEXANE)]-4-ONE, 4′-Methylbi(cyclohexyl)-4-one, SCHEMBL10861500, SCHEMBL10861505, DTXSID60603899, RHUNWKYRWMYYMP-UHFFFAOYSA-N, DTXSID701275508, 4-(4-methylcyclohexyl)cyclohexanone, AKOS006288119, AKOS030228380, BS-18930, 4′-Methyl[1,1′-bi(cyclohexane)]-4-one, F16473, trans-4a(2)-Methyl[1,1a(2)-bicyclohexyl]-4-one

4-(trans-4-Methylcyclohexyl)cyclohexanone serves as a key intermediate in the synthesis of liquid crystal displays (LCDs) due to its rigid bicyclic structure and optimal thermal stability. It is also employed in fragrance manufacturing, contributing to woody-amber olfactory profiles. Researchers utilize this compound in asymmetric catalysis and stereoselective reactions, leveraging its defined trans-configuration. Additionally, it finds use in polymer science as a crosslinking agent for specialty resins.

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