37593-02-5

Basic information

• Product Name: 4'-n-Amylacetophenone
• Synonyms: 1-(4-pentylphenyl)-ethanon;Acetophenone, 4'-pentyl-;Ethanone, 1-(4-pentylphenyl)-;p-n-Pentylacetophenone;P-AMYL ACETOPHENONE;P-PENTYLACETOPHENONE;TIMTEC-BB SBB007687;LABOTEST-BB LT00159042
• CAS NO: 37593-02-5
• Molecular Formula: C₁₃H₁₈O
• Molecular Weight: 190.28
• Product Categories: Acetophenones (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials
• Mol File: 37593-02-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 132-133°C 4mm
• Flash Point: 132-133°C/4mm
• Appearance: /
• Density: 0,95 g/cm3
• Vapor Pressure: 0.00187mmHg at 25°C
• Refractive Index: 1.5140 to 1.5160
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4'-n-Amylacetophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-n-Amylacetophenone(37593-02-5)
• EPA Substance Registry System: 4'-n-Amylacetophenone(37593-02-5)

Safety Data

• TSCA: Yes
• Hazardous Substances Data: 37593-02-5(Hazardous Substances Data)

Usage

Chemical Properties

Light yellow transparent liquid

Uses

Intermediates of Liquid Crystals

InChI:InChI=1/C13H18O/c1-3-4-5-6-12-7-9-13(10-8-12)11(2)14/h7-10H,3-6H2,1-2H3

Upstream product

• 538-68-1 pentylbenzene 
• 75-36-5 acetyl chloride 
• 10270-29-8 p-n-pentylbenzonitrile 
• 75-16-1 methylmagnesium bromide 
• 127570-89-2 1-(4-Pentyl-phenyl)-octadecan-1-one 
• 26311-45-5 4-pentylbenzoic acid 
• 49763-65-7 4-pentylbenzoyl chloride 
• 138913-07-2 4-n-pentylbenzamide 
• 766-04-1 benzyllithium 
• 79887-10-8 1-ethynyl-4-(n-pentyl)benzene 

Downstream Products

• 14377-21-0 4-pentylphenylethanoic acid 
• 14333-95-0 4-pentylbenzoylformaldehyde 
• 107727-11-7 6-(4-Pentyl-phenyl)-nicotinonitrile 
• 107487-96-7 2-Oxo-6-(4-pentyl-phenyl)-1,2-dihydro-pyridine-3-carbonitrile 
• 107488-07-3 2-Chloro-6-(4-pentyl-phenyl)-nicotinonitrile 
• 94775-80-1 3-(4-Pentyl-phenyl)-6-propyl-pyridazine 
• 94775-70-9 2-Hydroxy-1-(4-pentyl-phenyl)-heptane-1,4-dione 
• 94775-61-8 Potassium; 2-[1-hydroxy-2-oxo-2-(4-pentyl-phenyl)-ethyl]-3-oxo-hexanoate 

Relevant articles and documents

Mesogenic Properties of Copper(II) Complexes formed from α-Substituted β-Dialdehydes and β-Diketones

The relationship between molecular structure and mesogenic properties is explored for copper(II) complexes of α-substituted β-dialdehydes and β-diketones.The copper(II) complex of p-pentylphenylmalonaldehyde shows a nematic phase, but the presence of off-

Catalyst-free hydrochlorination protocol for terminal arylalkynes with hydrogen chloride

We present a simple and straightforward protocol for hydrochlorination of terminal arylalkynes to vinyl chlorides using hydrogen chloride under mild reaction conditions. This protocol does not involve any metal catalysts or additives. It is simple, inexpensive, and easy to prepare, and exhibits good reaction activity. The hydrochlorination proceeds smoothly to yield unique regioselective products via the Markovnikov addition rule.

Synthesis and Liquid Crystalline Phases of Pyridazine Derivatives II

Four more pyridazine compounds were synthesized.The compounds have a general structure R-X-Y-Z-R'; where Y is 3,6 disubstituted pyridazine ring, X and Z are either trans cyclohexyl or phenyl rings, R and R' are n-alkyl groups.The structure assignments were confirmed by carbon 13 NMR.Their liquid crystalline properties were evaluated.When both X and Z are cyclohexyl rings, the compounds have a single smectic b phase.However, if a phenyl ring is introduced into the system, the morphology becomes complicated.Keywords: synthesis, pyridazine, smectic, classification