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

Chemical Properties

Clear Colourless Liquid

Uses

Different sources of media describe the Uses of 2932-65-2 differently. You can refer to the following data:
1. A semivolatile compound found in waste landfill leachates. It is used as an intermediate in the preparation of STN liquid crystals for display devices
2. Intermediates of Liquid Crystals
3. 1-(4-Propylphenyl)ethan-1-one is a semivolatile compound found in waste landfill leachates , it is used as an intermediate in the preparation of STN liquid crystals for display devices.

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

• 17745-45-8 propylboronic acid 
• 99-90-1 para-bromoacetophenone 
• 62452-73-7 1-ethynyl-4-propylbenzene 
• 2550-26-7 4-Phenyl-2-butanone 
• 134150-01-9 4-propylphenylboric acid 
• 20024-90-2 p-(n-propyl)ethylbenzene 
• 62926-84-5 1-(4-allylphenyl)ethanone 
• 17417-03-7 1-<4'-Acetyl-phenyl>-propen 
• 77047-87-1 isopropyl zinc bromide 
• 7446-70-0 aluminium trichloride 
• 109-60-4 1-Propyl acetate 
• 71-43-2 benzene 
• 127570-75-6 p-propyl nonadecanophenone 
• 103-65-1 phenylpropane 

Downstream Products

• 369363-64-4 4-(4-propylphenyl)-1H-1,2,3-triazole 
• 199102-69-7 3-oxo-3-(4-propylphenyl)propanenitrile 

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.