131906-57-5

Basic information

• Product Name: 1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE
• Synonyms: 1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE;1-(4-Hexyphenyl)-2-propane-1-one;cpd L3, L3 Antagonist TR-SIR-2
• CAS NO: 131906-57-5
• Molecular Formula: C₁₅H₂₀O
• Molecular Weight: 216.3187
• Mol File: 131906-57-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 320.627°C at 760 mmHg
• Flash Point: 133.809°C
• Appearance: /
• Density: 0.935g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.506
• Storage Temp.: −20°C
• Solubility: DMSO: >5mg/mL
• CAS DataBase Reference: 1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE(131906-57-5)
• EPA Substance Registry System: 1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE(131906-57-5)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 3
• Hazardous Substances Data: 131906-57-5(Hazardous Substances Data)

Usage

Description

1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE, also known as para-hexylphenyl acrylketone, is a chemical compound characterized by its molecular formula C15H20O. It is a yellow, oily liquid with a distinct floral and herbal scent. 1-(4-HEXYLPHENYL)-2-PROPEN-1-ONE is recognized for its diverse applications across various industries, including the perfume, food, cosmetic, and pharmaceutical sectors.

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 articles and documents

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

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.