16618-75-0

Basic information

• Product Name: 4-Heptylcyclohexanone
• Synonyms: 4-Heptylcyclohexanone;Cyclohexanone, 4-heptyl-
• CAS NO: 16618-75-0
• Molecular Formula: C₁₃H₂₄O
• Molecular Weight: 196.32906
• Mol File: 16618-75-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 118-120 °C(Press: 5 Torr)
• Appearance: /
• Density: 0.880±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-Heptylcyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Heptylcyclohexanone(16618-75-0)
• EPA Substance Registry System: 4-Heptylcyclohexanone(16618-75-0)

Safety Data

• Hazardous Substances Data: 16618-75-0(Hazardous Substances Data)

Usage

Chemical Properties

Colorless liquid

Upstream product

• 127562-52-1 4-[(E)-non-1-en-1-yl]morpholine 
• 1987-50-4 p-heptylphenol 
• 98789-92-5 4-heptylcyclohexenone 
• 106377-16-6 cis and trans mixture of 4-heptylcyclohexanol 
• 124-19-6 nonan-1-al 

Downstream Products

• 1065272-72-1 4-heptyl-1-(3-fluorophenyl)-cyclohexanol 
• 82254-85-1 4-Heptyl-2-(3-oxo-butyl)-cyclohexanone 
• 107268-77-9 2-methyl-5-<(4-heptyl-1-hydroxycyclohexyl)ethyl>pyridine 
• 107268-85-9 2-hydroxymethyl-5-<(4-heptylcyclohexyl)ethyl>pyridine 
• 107534-74-7 2-methyl-5-<(4-heptyl-1-cyclohexenyl)ethyl>pyridine 
• 107268-83-7 5-[2-(4-Heptyl-cyclohexyl)-ethyl]-2-methyl-pyridine 1-oxide 
• 107268-81-5 2-methyl-5-<(4-heptylcyclohexyl)ethyl>pyridine 
• 73163-48-1 4-(4-Heptyl-cyclohexyl)-benzamide 
• 61203-98-3 trans-4-heptyl-1-phenylcyclohexane 
• 88069-98-1 (4-n-heptylcyclohexen-1-yl)-benzene 
• 78531-60-9 4-(trans-4-n-heptylcyclohexyl)acetophenone 
• 81930-19-0 trans-4-(4-Heptylcyclohexyl)benzoesaeurechlorid 
• 65355-31-9 4'-benzoesaeure 
• 61204-03-3 4-(trans-4-heptylcyclohexyl)benzonitrile 

Relevant articles and documents

The Synthesis and Liquid Crystal Behavior of p-Benzotrifluoride Compounds I

Three compounds with the R-X-Y-CF3 structure were synthesized where X is a trans cyclohexil ring.Y is a benzene ring and R is an alkyl group.The structure assignments were confirmed by carbon 13NMR and the compounds were purified by preparative liquid chromatography.The separation of cis and trans isomers of 1-p-trifluorophenyl-4-alkyl-cyclohexanol is also discussed.Although these compounds do not have a liquid crystalline phase themselves, a liquid crystal mixture containing them shows a much faster turn off speed than materials without them.Keywords: benzotrifluoride, trifluoromethyl, time response, TN cell