37593-06-9

Usage

Uses

Used in Perfumery and Fragrance Industry:
1-(4-Decylphenyl)ethan-1-one is used as a key ingredient in the production of perfumes and fragrances for its pleasant and long-lasting odor, enhancing the sensory experience of various products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1-(4-decylphenyl)ethan-1-one is utilized in the synthesis of various pharmaceuticals, leveraging its chemical properties to contribute to the development of new medications.
Used as a Flavoring Agent in Food Industry:
1-(4-Decylphenyl)ethan-1-one is employed as a flavoring agent in food products, imparting unique taste profiles and enhancing the overall flavor experience for consumers.
Used in Organic Synthesis and Material Science:
1-(4-DECYLPHENYL)ETHAN-1-ONE also has potential applications in the field of organic synthesis and material science, where its chemical structure can be manipulated to create new materials or intermediates for various uses.
Overall, 1-(4-decylphenyl)ethan-1-one's versatility in different industries is a testament to its unique chemical properties and the wide range of applications it supports.

InChI:InChI=1/C18H28O/c1-3-4-5-6-7-8-9-10-11-17-12-14-18(15-13-17)16(2)19/h12-15H,3-11H2,1-2H3

Upstream product

• 107678-20-6 2-(4-Decyl-phenyl)-2-methyl-[1,3]dithiane 
• 104-72-3 decylbenzene 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Downstream Products

• 38300-04-8 4-decylbenzoic acid 
• 69511-08-6 1-(4-decylphenyl)ethan-1-ol 
• 78450-46-1 1,3-Di(p-n-decylphenyl)propane-1,3-dione 
• 134444-34-1 1-(p-n-decylphenyl)3-(p-n-decyloxyphenyl)propane-1,3-dione 
• 37593-13-8 N-(4-decylphenyl)acetamide 
• 16877-72-8 4-n-decyl-α-bromoacetophenone 
• 46926-59-4 1-decyl-4-vinylbenzene 
• 78575-35-6 (4-Decyl-phenyl)-[(E)-hydroxyimino]-acetaldehyde oxime 
• 94775-85-6 3-(4-Decyl-phenyl)-6-propyl-pyridazine 
• 94775-75-4 1-(4-Decyl-phenyl)-2-hydroxy-heptane-1,4-dione 
• 94775-66-3 Potassium; 2-[2-(4-decyl-phenyl)-1-hydroxy-2-oxo-ethyl]-3-oxo-hexanoate 
• 83471-22-1 4-decyl-3-nitro-benzoic acid 
• 53097-42-0 3-(4-Decyl-phenyl)-3-oxo-propionic acid methyl ester 

Relevant academic research and scientific papers

Syndiospecific synthesis of longer p-n-alkyl-substituted polystyrenes using monocyclopentadienyl-type titanium catalysts

Substituted styrenes with linear alkyl substituents (C6 to C12) at the para position on the ring were synthesized and polymerized using the (Me)5CpTi(OMe)3/MAO catalytic system. Increased polymerization activiti

Nouveaux diamino-3,4 phenylalcanes et leur transformation en benzimidazolemethanethiols-2

We report five o-phenylenediamines which are substituted by an aliphatic chain containing n carbon atoms (n = 4, 6, 8, 10, 12).We describe a well adapted general synthetic method using Schmidt's reaction.The diamines were then transformed into 2-benzimidazolemethanethiols and their related S-methyl derivatives which structures were checked by (1)H NMR.

DETHIOACETALISATION DE DITHIANNES-1,3 PAR DES TRIBROMURES DE PHOSPHONIUM

Methyltriphenylphosphonium tribromide 1 acts as an efficient mild dethioketalization reagent with high selectivity for 2-phenyl and 2-vinyl 1,3-dithiannes 2 versus 2-alkyl 1,3-dithiannes and without any secondary bromination reaction of the investigated substrates.The reaction was also succesful with trimethylphenylammonium tribromide.

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.

Multiple Melting Behaviour in Square-planar trans-Bis-(1-p-n-alkylphenylbutane-1,3-dionato)copper(II) - The Effect of Alkyl Chain Length

The title complexes having different n-alkyl groups from methyl to dodecyl have synthesized.All these complexes exhibit solid polymorphism.The number of polymorphs depends on the length of the alkyl chain: two for n (the number of carbon atoms) = 0-2, three for n = 3-5 and 12, and four for n = 6-11, respectively.Each polymorphic form except those with the highest m.p.s. exhibits multiple melting behaviour: double melting for n = 0-5,8, and 12, and triple melting for n = 6-11 except 8.The m.p.s. of the complexes with alkyl groups of odd carbon atoms are higher than those with even atoms, while the respective ligand solids show the opposit e even-odd effect in their m.p.s.

Study of the Influence of Molecular Length on the Characteristics of the Ordered Smectic Phase.

Study of DTA and X-rays of p-phenyl-benzylidene-p'-alkylanilines of mesomorphic phases demonstrates the predominant role of the aliphatic chain length. In effect, it governs the appearance of the different phases; the correlation between layers decreases for greater chain lengths. The nonlinear variations of SmB layer thickness for these compounds shows clearly the importance of steric effects coupled with the molecular length with respect to the dipolar effect.