51171-73-4

Basic information

• Product Name: 4-Hydroxy-4-phenylcyclohexanone
• Synonyms: 4-Hydroxy-4-phenylcyclohexanone
• CAS NO: 51171-73-4
• Molecular Formula: C₁₂H₁₄O₂
• Molecular Weight: 190.23836
• Mol File: 51171-73-4.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 349.9°C at 760 mmHg
• Flash Point: 149.1°C
• Appearance: /
• Density: 1.17g/cm³
• Vapor Pressure: 1.71E-05mmHg at 25°C
• Refractive Index: 1.575
• CAS DataBase Reference: 4-Hydroxy-4-phenylcyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Hydroxy-4-phenylcyclohexanone(51171-73-4)
• EPA Substance Registry System: 4-Hydroxy-4-phenylcyclohexanone(51171-73-4)

Safety Data

• Hazardous Substances Data: 51171-73-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H14O2/c13-11-6-8-12(14,9-7-11)10-4-2-1-3-5-10/h1-5,14H,6-9H2

Upstream product

• 591-51-5 phenyllithium 
• 637-88-7 1,4-Cyclohexanedione 
• 94112-58-0 4-hydroxy-4-phenyl-cyclohexanone ethylene ketal 
• 678967-25-4 3-(1-Phenyl-vinyl)-1,2,5-trioxaspiro[5.5]undec-9-one 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 80770-73-6 1-phenyl-4-hydroxycyclohexanol 
• 100-58-3 phenylmagnesium bromide 
• 613-37-6 4-methoxylbiphenyl 
• 108-86-1 bromobenzene 
• 13482-22-9 4-hydroxycyclohexanone 

Downstream Products

• 77611-99-5 1,4-Dihydroxy-4-phenylcyclohexancarbonitril 
• 70353-42-3 1-phenyl-5-hexene-1,4-dione 
• 51171-71-2 4-phenyl-3-cyclohexen-1-one 
• 2920-38-9 4-cyano-1,1'-biphenyl 
• 77612-00-1 4-Phenyl-1,3-cyclohexadien-1-carbonitril 
• 77612-04-5 2-phenylfuran-3-carbonitrile 
• 77612-05-6 1-Phenyl-2-oxabicyclo<3.2.0>hept-3-en-5-carbonitril 
• 77611-98-4 1-Phenyl-7-oxabicyclo<4.1.0>hept-4-en-4-carbonitril 
• 77612-07-8 4-Cyan-N,1-diphenyl-9-oxabicyclo<4.2.1>non-4-en-7,8-dicarboximid 
• 15619-51-9 4-hydroxy-1-phenylcyclohexene 
• 1056990-59-0 4-(nitromethyl)-1-phenylcyclohex-3-en-1-ol 
• 393138-28-8 C₁₂H₁₄O₃ 
• 1220393-30-5 C₁₉H₂₃NO 

Relevant articles and documents

Application of Transaminases in a Disperse System for the Bioamination of Hydrophobic Substrates

The challenging bioamination of hydrophobic substrates has been attained through the employment of a disperse system consisting of a combination of a low polarity solvent (e. g. isooctane or methyl-tert-butylether), a non-ionic surfactant and a minimal amount of water. In these conditions, amine transaminases (ATA) were shown to efficiently carry out the reductive amination of variously substituted cyclohexanones, providing good conversions often coupled with a superior stereoselectivity if compared with the corresponding chemical reductive amination. An array of synthetically useful 4-substituted aminocyclohexanes was consequentially synthesized through biocatalysis, analyzed and stereochemically characterized. (Figure presented.).

Optimization of TRPV6 calcium channel inhibitors using a 3D ligand-based virtual screening method

Herein, we report the discovery of the first potent and selective inhibitor of TRPV6, a calcium channel overexpressed in breast and prostate cancer, and its use to test the effect of blocking TRPV6-mediated Ca2+-influx on cell growth. The inhib

A METHOD OF TREATING LIVER FIBROSIS

The present invention relates to a method of treating hepatis C and/or liver fibroisis with 3-cycloalkylaminopyrrolidine derivatives of the present invention