2932-65-2

Basic information

• Product Name: 1-(4-Propylphenyl)ethan-1-one
• Synonyms: LABOTEST-BB LT00159020;4'-N-PROPYLACETOPHENONE;4-N-PROPYLACETOPHENONE;4'-PROPYLACETOPHENONE;4-PROPYLACETOPHENONE;1-(4-PROPYLPHENYL)ETHAN-1-ONE;1-(4-PROPYL-PHENYL)ETHANONE;P-PROPYLACETOPHENONE
• CAS NO: 2932-65-2
• Molecular Formula: C₁₁H₁₄O
• Molecular Weight: 162.23
• EINECS: 220-903-5
• Product Categories: Aromatic Acetophenones & Derivatives (substituted);Acetophenones (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials;Aromatics;Intermediates
• Mol File: 2932-65-2.mol
• Article Data: 24

Chemical Properties

• Boiling Point: 123-125°C (15 mmHg)
• Flash Point: 251-252°C
• Appearance: Clear colourless liquid
• Density: 0,98 g/cm3
• Vapor Pressure: 0.0145mmHg at 25°C
• Refractive Index: 1.5225
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Methanol
• BRN: 1858604
• CAS DataBase Reference: 1-(4-Propylphenyl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Propylphenyl)ethan-1-one(2932-65-2)
• EPA Substance Registry System: 1-(4-Propylphenyl)ethan-1-one(2932-65-2)

Safety Data

• Hazard Codes: Xn,Xi
• Statements: 22-36/37/38
• Safety Statements: 23-26-36/37/39-24/25
• Hazardous Substances Data: 2932-65-2(Hazardous Substances Data)

Usage

Description

1-(4-Propylphenyl)ethan-1-one is a clear, colorless liquid that is a semivolatile compound found in waste landfill leachates. It is characterized by its unique chemical structure, which contributes to its various applications in different industries.

Uses

1. Used in Display Device Industry:
1-(4-Propylphenyl)ethan-1-one is used as an intermediate in the preparation of STN (Super Twisted Nematic) liquid crystals for display devices. Its role in the production process is crucial for creating high-quality displays with improved performance characteristics.
2. Used in Chemical Synthesis:
As an intermediate in chemical synthesis, 1-(4-Propylphenyl)ethan-1-one is utilized for the production of various compounds and materials. Its versatility in chemical reactions makes it a valuable component in the synthesis of different products.
3. Used in Environmental Monitoring:
Due to its presence in waste landfill leachates, 1-(4-Propylphenyl)ethan-1-one can be used as a marker or indicator for monitoring the environmental impact of waste disposal sites. This application helps in assessing the effectiveness of waste management practices and the potential risks associated with landfill leachates.

InChI:InChI=1/C11H14O/c1-3-4-10-5-7-11(8-6-10)9(2)12/h5-8H,3-4H2,1-2H3

Upstream product

• 103-65-1 phenylpropane 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 109-60-4 1-Propyl acetate 
• 71-43-2 benzene 
• 127570-75-6 p-propyl nonadecanophenone 
• 7446-70-0 aluminium trichloride 
• 17745-45-8 propylboronic acid 
• 99-90-1 para-bromoacetophenone 
• 77047-87-1 isopropyl zinc bromide 
• 62452-73-7 1-ethynyl-4-propylbenzene 
• 17417-03-7 1-<4'-Acetyl-phenyl>-propen 
• 62926-84-5 1-(4-allylphenyl)ethanone 
• 2550-26-7 4-Phenyl-2-butanone 

Downstream Products

• 108298-96-0 4-(4-acetyl-phenyl)-3-methyl-but-3-en-2-one 
• 107549-80-4 6-(4-propylphenyl)pyridazin-3(2H)-one 
• 91339-01-4 (RS)-1-(p-n-propylphenyl)ethylamine 
• 100-21-0 terephthalic acid 
• 212968-68-8 (S)-1-(p-n-propylphenyl)ethylamine 
• 212968-68-8 (R)-1-(4-Propyl-phenyl)-ethylamine 
• 105364-41-8 rac-1-(4-propylphenyl)ethanol 
• 105364-41-8 (S)-1-(4'-propylphenyl)ethanol 
• 105364-41-8 (R)-1-(4'-propylphenyl)ethanol 
• 199171-93-2 3-nitro-4-propyl-benzoic acid 
• 2438-05-3 4-n-propylbenzoic acid 

Relevant articles and documents

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Selective electrochemical oxidation of aromatic hydrocarbons and preparation of mono/multi-carbonyl compounds

A selective electrochemical oxidation was developed under mild condition. Various mono-carbonyl and multi-carbonyl compounds can be prepared from different aromatic hydrocarbons with moderate to excellent yield and selectivity by virtue of this electrochemical oxidation. The produced carbonyl compounds can be further transformed into α-ketoamides, homoallylic alcohols and oximes in a one-pot reaction. In particular, a series of α-ketoamides were prepared in a one-pot continuous electrolysis. Mechanistic studies showed that 2,2,2-trifluoroethan-1-ol (TFE) can interact with catalyst species and generate the corresponding hydrogen-bonding complex to enhance the electrochemical oxidation performance. [Figure not available: see fulltext.]

Synthesis method of primary amine hydrochloride

The invention discloses a synthesis method of primary amine hydrochloride. According to the synthesis method, in the presence of a gold complex, water and alkyne carry out catalytic hydrolysis to generate ketones, and then ketones and ammonium formate are catalyzed by a rhodium complex to generate primary amine. Compared with a conventional primary amine synthesis method, the synthesis method hasthe advantages that no alkali is added during the reaction process, no side product is generated, the atomic economy is good, the reaction conditions are mild, and the synthesis method has a wide prospect.