trans-4-(p-Chlorophenyl)-1-acetylcyclohexane

Base Information

• Chemical Name: trans-4-(p-Chlorophenyl)-1-acetylcyclohexane
• CAS No.: 91161-85-2
• Molecular Formula: C14H17ClO
• Molecular Weight: 236.74
• UNII: T52V62EK78,KVS452J2KN
• Mol file: 91161-85-2.mol

Synonyms:91161-85-2;trans-4-(p-Chlorophenyl)-1-acetylcyclohexane;95233-36-6;TRANS-4-(4-CHLOROPHENYL)-1-ACETYLCYCLOHEXANE;1-[4-(4-chlorophenyl)cyclohexyl]ethanone;4'-Acetylcyclohexyl chlorobenzene;1-(4-(4-Chlorophenyl)cyclohexyl)ethanone;cis-4-(4-Chlorophenyl)-1-acetylcyclohexane;1-[(1r,4r)-4-(4-chlorophenyl)cyclohexyl]ethan-1-one;1-(4-(4-chlorophenyl)cyclohexyl)ethan-1-one;1-[4-(4-chlorophenyl)cyclohexyl]ethan-1-one;Atovaquone Impurity 1;Atovaquone Impurity 3;cis-4-(p-Chlorophenyl)-1-acetylcyclohexane;KVS452J2KN;Ethanone, 1-[trans-4-(4-chlorophenyl)cyclohexyl]-;SCHEMBL1837178;SCHEMBL3219203;FLHSIPCMAJDSGB-HAQNSBGRSA-N;T52V62EK78;AKOS015961715;AC-14592;DB-361753;Ethanone, 1-[4-(4-chlorophenyl)cyclohexyl]-;trans-4-(4-chlorophenyl)cyclohexyl-1-ethanone;trans-4-(p-chlorophenyl)-1-acetyl-cyclohexane;1-[trans-4-(4-Chlorophenyl)cyclohexyl]ethanone;4-(4-Chlorophenyl)-1-acetylcyclohexane, trans-;Ethanone, 1-[4-(4-chlorophenyl)cyclohexyl]-, trans-;cis-1-[4-(4-chlorophenyl)cyclohexyl]ethanone,1-[cis-4-(4-Chlorophenyl)cyclohexyl]ethanone

Chemical Property of trans-4-(p-Chlorophenyl)-1-acetylcyclohexane

Chemical Property:

• PSA: 17.07000
• Density: 1.107
• LogP: 4.20280
• XLogP3: 3.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 236.0967929
• Heavy Atom Count: 16
• Complexity: 235

Purity/Quality:

99% ^*data from raw suppliers

trans-4-(4-Chlorophenyl)-1-acetylcyclohexane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(=O)C1CCC(CC1)C2=CC=C(C=C2)Cl
• Uses: trans-4-(4-Chlorophenyl)-1-acetylcyclohexane is an intermediate used to prepare 2-(4-(4-chlorophenyl)cyclohexyl)-3-hydroxy-1,4-naphthoquinone for the treatment of cancer. It is also used in the synthesis of aminothiazole derivatives as inhibitors of action of AgRP on a melanocortin receptor.