37593-03-6

Basic information

• Product Name: 4'-N-HEPTYLACETOPHENONE
• Synonyms: 1-(4-heptylphenyl)-ethanon;Ethanone, 1-(4-heptylphenyl)-;p-n-Heptylacetophenone;SALOR-INT L168963-1EA;P-HEPTYLACETOPHENONE;TIMTEC-BB SBB008311;4'-N-HEPTYLACETOPHENONE;4-N-HEPTYLACETOPHENONE
• CAS NO: 37593-03-6
• Molecular Formula: C₁₅H₂₂O
• Molecular Weight: 218.33
• EINECS: 253-560-5
• Product Categories: Acetophenones (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials
• Mol File: 37593-03-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 155 °C
• Flash Point: 155-157°C/2mm
• Appearance: /
• Density: 0,94 g/cm3
• Vapor Pressure: 0.000237mmHg at 25°C
• Refractive Index: 1.5090
• BRN: 1866760
• CAS DataBase Reference: 4'-N-HEPTYLACETOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-N-HEPTYLACETOPHENONE(37593-03-6)
• EPA Substance Registry System: 4'-N-HEPTYLACETOPHENONE(37593-03-6)

Safety Data

• Safety Statements: 24/25
• TSCA: Yes
• Hazardous Substances Data: 37593-03-6(Hazardous Substances Data)

Usage

General Description

4'-N-Heptylacetophenone is a chemical compound with the molecular formula C16H24O. It belongs to the class of acetophenone derivatives and is commonly used in the synthesis of pharmaceuticals and as a flavoring agent in food and beverages. It is a clear, yellow liquid with a strong, sweet, and floral odor. 4'-N-Heptylacetophenone is known for its antimicrobial properties and is often used as an ingredient in personal care products such as lotions and soaps. It is also used as a fragrance in perfumes and colognes. Additionally, it has potential applications in the agricultural industry as a pesticide or insect repellent due to its aromatic properties.

InChI:InChI=1/C15H22O/c1-3-4-5-6-7-8-14-9-11-15(12-10-14)13(2)16/h9-12H,3-8H2,1-2H3

Upstream product

• 2528-61-2 Heptanoic acid chloride 
• 186581-53-3 diazomethane 
• 50606-96-7 4-heptylbenzoyl chloride 
• 4282-40-0 1-Iodoheptane 
• 99-90-1 para-bromoacetophenone 
• 1671-75-6 Heptanophenone 
• 629-04-9 1-Bromoheptane 
• 108-86-1 bromobenzene 
• 1078-71-3 heptylbenzene 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 

Downstream Products

• 100-21-0 terephthalic acid 
• 1359983-63-3 C₁₆H₂₃N₃*ClH 
• 1359983-81-5 C₂₁H₃₁N₃O₂ 
• 81539-62-0 C₄₆H₅₂N₈ 
• 81539-67-5 4-(4-Heptyl-phenyl)-N¹-[1-phenyl-meth-(Z)-ylidene]-imidazole-1,2-diamine 
• 81518-57-2 4-(4-Heptyl-phenyl)-imidazole-1,2-diamine 
• 94775-63-0 Potassium; 2-[2-(4-heptyl-phenyl)-1-hydroxy-2-oxo-ethyl]-3-oxo-hexanoate 
• 94775-72-1 1-(4-Heptyl-phenyl)-2-hydroxy-heptane-1,4-dione 
• 94775-82-3 3-(4-Heptyl-phenyl)-6-propyl-pyridazine 
• 88053-97-8 6-(4-Heptyl-phenyl)-2-oxo-2H-pyran-3-carboxylic acid ethyl ester 
• 537021-55-9 11-[pentakis(4-heptylphenylethynyl)phenoxy]undecan-1-ol 
• 79887-12-0 1-ethynyl-4-heptylbenzene 
• 107488-09-5 2-Chloro-6-(4-heptyl-phenyl)-nicotinonitrile 
• 107487-98-9 6-(4-Heptyl-phenyl)-2-oxo-1,2-dihydro-pyridine-3-carbonitrile 

Relevant articles and documents

Reevaluation of the Palladium/Carbon-Catalyzed Decarbonylation of Aliphatic Aldehydes

An improved method for the decarbonylation of aliphatic aldehydes by using a commercially available Pd/C catalyst is described. The reaction conditions are suitable for linear, cyclic, or sterically demanding substrates, as they afford the corresponding alkanes in yields of up to 99%. In addition, this Pd/C-catalyzed method exhibits good functional-group tolerance. A comparison of previously reported methods with the present one showed that the reaction conditions play a crucial role in the outcome of the reaction. The method can also be applied in a two-step reaction sequence for the synthesis of industrially important compounds.

Zn-mediated, Pd-catalyzed cross-couplings in water at room temperature without prior formation of organozinc reagents

(Chemical Equation Presented) Mix in water, stir. That is all that is required in this new approach to sp3-sp2 cross-couplings between an alkyl iodide and an aryl bromide, both potentially bearing functionality. They react under cata

The Synthesis of 3-Aryl-6-alkylpyridazines

Nine compounds of general structure R-X-Y-R' where X is a para-disubstituted phenyl ring and Y is a 3,6-disubstituted-pyridazine ring were synthesized.These can be used as liquid crystal dopents.A general procedure for their synthesis was developed.N-Alkyl benzene and ethyl butyrylacetate were used as starting materials.The purification of reaction intermediates was not necessary if preparative hplc was used to purify the final products.Very pure materials were obtained with good yield.Their structure was confirmed by carbon 13 nmr.