4537-14-8

Basic information

• Product Name: 6-phenylundecane
• Synonyms: 6-phenylundecane;(1-Pentylhexyl)benzene
• CAS NO: 4537-14-8
• Molecular Formula: C₁₇H₂₈
• Molecular Weight: 232.4042
• Mol File: 4537-14-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 306.5°Cat760mmHg
• Flash Point: 134.3°C
• Appearance: /
• Density: 0.855g/cm³
• Vapor Pressure: 0.00139mmHg at 25°C
• Refractive Index: 1.482
• CAS DataBase Reference: 6-phenylundecane(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenylundecane(4537-14-8)
• EPA Substance Registry System: 6-phenylundecane(4537-14-8)

Safety Data

• Hazardous Substances Data: 4537-14-8(Hazardous Substances Data)

Usage

Definition

ChEBI: An alkylbenzene comprising undecane substituted at position 6 by a phenyl group.

InChI:InChI=1/C17H28/c1-3-5-8-12-16(13-9-6-4-2)17-14-10-7-11-15-17/h7,10-11,14-16H,3-6,8-9,12-13H2,1-2H3

Upstream product

• 71-43-2 benzene 
• 927-49-1 dipentyl ketone 
• 108-86-1 bromobenzene 
• 628-17-1 amyl iodide 
• 100-52-7 benzaldehyde 
• 89579-51-1 6-phenyl-5-undecene 
• 67267-86-1 6-phenyl-6-undecanol 
• 93-89-0 benzoic acid ethyl ester 
• 693-25-4 n-pentylmagnesium bromide 

Relevant articles and documents

Process for the production of phenylalkanes using a hydrocarbon fraction that is obtained from the Fischer-Tropsch process

A process for the production of phenylalkanes comprising a reaction for alkylation of at least one aromatic compound by at least one hydrocarbon fraction that is directly obtained from the Fischer-Tropsch process comprising linear olefins that have 9 to 16 carbon atoms per molecule and oxygenated compounds is described. Said alkylation reaction is carried out in a catalytic reactor that contains at least one reaction zone that comprises at least one acidic solid catalyst, and said hydrocarbon fraction does not undergo any purification treatment prior to its introduction into said reaction zone.

Synthesis of Trialkylacetic Acids by the Anodic Oxidation of 3,3-Disubstituted-2-oxo Carboxylic Acids

The "non-Kolbe" electrolysis of 3,3-disubstituted-2-oxocarboxylates 1-3 in methanol produced mixtures of methyl trialkylacetates 5, trialkylacetaldehydes 6, in some cases 2-hydroxy-3,3,3-trialkylpropionic acids 7, trialkylethylenes 8, and methyl trialkylmethyl ethers 9.When one of the substituents on the 3-carbon of the 2-oxo carboxylate was phenyl 4, molecular rearrangement was not observed.In addition to products 5-9, with the exception of 7, there was obtained with 4 an alkyl phenyl ketone 10.The methyl trisubstituted acetates were saponified to the desired trialkylacetic acids.