131906-57-5

Usage

Uses

Used in Perfumery:
1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE is used as a fragrance ingredient for its floral and herbal odor, contributing to the creation of various perfumes and colognes.
Used in the Food Industry:
In the food industry, 1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE is used as a flavoring agent, enhancing the taste and aroma of different food products.
Used in Cosmetics:
1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE is used as an ingredient in the formulation of sunscreens and other cosmetic products, benefiting from its scent and potential protective properties.
Used in Pharmaceutical Research:
1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE is studied for its potential biological activities, such as anti-inflammatory and antioxidant properties, which may lead to its use in the development of pharmaceutical products.

InChI:InChI=1/C15H20O/c1-3-5-6-7-8-13-9-11-14(12-10-13)15(16)4-2/h4,9-12H,2-3,5-8H2,1H3

Upstream product

• 131906-71-3 1-(4-Hexyl-phenyl)-2-phenylselanyl-propan-1-one 
• 1077-16-3 hexylbenzene 
• 814-68-6 acryloyl chloride 
• 79219-16-2 1-(4-hexyl-phenyl)-propan-1-one 

Downstream Products

• 131906-66-6 {6-[(1R,4R)-4-(4-Hexyl-benzenesulfonyl)-5-(4-hexyl-benzoyl)-cyclohex-2-enylcarbamoyloxy]-hexyl}-trimethyl-ammonium; bromide 
• 131906-59-7 6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide 
• 131932-54-2 6-<<<-2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide 
• 131906-68-8 benzyl (cis-6-(4-hexylbenzoyl)-cis-4-(phenylsulfonyl)-2-cyclohexen-1-yl)carbamate 

Relevant academic research and scientific papers

Inhibitors of the interaction of a thyroid hormone receptor and coactivators: Preliminary structure-activity relationships

The modulation of gene regulation by blocking the interaction between the thyroid receptor (TR) and obligate coregulators has been reported recently with the discovery of the lead compound 3-(dimethylamino)-1-(4-hexylphenyl)propan-1- one). Herein we repor

Synthesis of quaternary alkylammonium sulfobetaines

A series of quaternary alkylammonium sulfobetaines of general formula RN+(CH3)2(CH2)nSO 3-, where n = 2-4, have been synthesised by reacting the corresponding N,N-dimethylamines with either sodium 2-chloroethanesulfonate (n = 2), 1,3-propane-sultone (n = 3), or 1,4-butanesultone (n = 4). Full details of the preparation of the required N,N-dimethylamines are reported.

Diels-Alder Reactions of a Surfactant 1,3-Diene

The ability of aqueous micelles and reversed micelles to control the regiochemistry of Diels-Alder reactions of (E,E)-6--1,3-butadienyl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide (4) and 1-(4-hexylphenyl)-2-propen-1-one (2b) was evaluated.If 2b and 4 were to react within the micelles in their preferred orientations, cycloadduct 10 would result, as opposed to 6--2-cyclohexen-1-yl>amino>carbonyl>oxy>-N,N,N-trimethyl-1-hexanaminium bromide (7b) and its exo isomer 8b, the theoretically predicted products actually obtained.The orientational effects in the aggregates were not strong enough to overcome the reaction's intrinsically preferred regiochemistry.