36716-71-9

Basic information

• Product Name: 4-(4-Chlorophenyl)-4-hydroxycyclohexanone
• Synonyms: 4-(p-Chlorophenyl)-4-hydroxycyclohexanone;4-(4-Chlorophenyl)-4-hydroxycyclohexanone
• CAS NO: 36716-71-9
• Molecular Formula: C₁₂H₁₃ClO₂
• Molecular Weight: 224.68342
• Product Categories: Aromatics
• Mol File: 36716-71-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 375.247°C at 760 mmHg
• Flash Point: 180.743°C
• Appearance: /
• Density: 1.288g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.587
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Methanol
• CAS DataBase Reference: 4-(4-Chlorophenyl)-4-hydroxycyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-Chlorophenyl)-4-hydroxycyclohexanone(36716-71-9)
• EPA Substance Registry System: 4-(4-Chlorophenyl)-4-hydroxycyclohexanone(36716-71-9)

Safety Data

• Hazardous Substances Data: 36716-71-9(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

4-(4-Chlorophenyl)-4-hydroxycyclohexanone (cas# 36716-71-9) is a compound useful in organic synthesis.

InChI:InChI=1/C12H13ClO2/c13-10-3-1-9(2-4-10)12(15)7-5-11(14)6-8-12/h1-4,15H,5-8H2

Upstream product

• 13482-22-9 4-hydroxycyclohexanone 
• 873-77-8 (4-chlorphenyl)magnesium bromide 
• 106-39-8 bromochlorobenzene 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 637-87-6 1-Chloro-4-iodobenzene 
• 126991-59-1 8-(4-chlorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol 

Downstream Products

• 42020-44-0 4-(p-chlorophenyl)-4-hydroxycyclohexanone dimethyl ketal 
• 36716-78-6 4-(p-chlorophenyl)-3-cyclohexen-1-ol 
• 36716-82-2 Methanesulfonic acid 4-(4-chloro-phenyl)-cyclohex-3-enyl ester 
• 1071223-07-8 cis-2-[4-(4-chlorophenyl)cyclohexyl]-3-chloro-1,4-naphthoquinone 
• 215672-87-0 Oxalic acid mono-[4-(4-chloro-phenyl)-cyclohexyl] ester 
• 98322-65-7 4-(4-Chloro-phenyl)-cyclohexanol 
• 14472-80-1 4-(4-chlorophenyl)cyclohexan-1-one 
• 73330-73-1 4-(p-Chlorophenyl)-4-hydroxycyclohexanone oxime 
• 73330-74-2 4-(p-Chlorophenyl)-4-hydroxycyclohexanone O-methyloxime 

Relevant articles and documents

All-benzene carbon nanocages: Size-selective synthesis, photophysical properties, and crystal structure

The design and synthesis of a series of carbon nanocages consisting solely of benzene rings are described. Carbon nanocages are appealing molecules not only because they represent junction unit structures of branched carbon nanotubes, but also because of their potential utilities as unique optoelectronic π-conjugated materials and guest-encapsulating hosts. Three sizes of strained, conjugated [n.n.n]carbon nanocages (1, n = 4; 2, n = 5; 3, n = 6) were synthesized with perfect size-selectivity. Cyclohexane-containing units and 1,3,5-trisubstituted benzene-containing units were assembled to yield the minimally strained bicyclic precursors, which were successfully converted into the corresponding carbon nanocages via acid-mediated aromatization. X-ray crystallography of 1 confirmed the cage-shaped structure with an approximately spherical void inside the cage molecule. The present studies revealed the unique properties of carbon nanocages, including strain energies, size-dependent absorption and fluorescence, as well as unique size-dependency for the electronic features of 1-3.

Synthesis of atovaquone

A short synthesis of atovaquone I is achieved via the radical coupling of the trans-1,4-substituted cyclohexyl mono-oxalate 2 and 2- chloronapthoquinone under phase transfer conditions.

4'-Fluoro-4-{[4-(phenyl)-4-alkoxy-cyclo-hexyl]amino}butyrophenones and the salts thereof

This invention relates to novel 4-(substituted alkoxy)-4-(substituted phenyl)cyclohexylamines embraced by the formula SPC1 Wherein ? is a generic expression denoting cis and trans stereoconfiguration and mixtures thereof, with the proviso that when the st