131906-57-5 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.
Check Digit Verification of cas no
The CAS Registry Mumber 131906-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,9,0 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131906-57:
(8*1)+(7*3)+(6*1)+(5*9)+(4*0)+(3*6)+(2*5)+(1*7)=115
115 % 10 = 5
So 131906-57-5 is a valid CAS Registry Number.
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
131906-57-5Relevant articles and documents
Inhibitors of the interaction of a thyroid hormone receptor and coactivators: Preliminary structure-activity relationships
Arnold, Leggy A.,Kosinski, Aaron,Estébanez-Perpi?á, Eva,Fletterick, Robert J.,Guy, R. Kiplin
, p. 5269 - 5280 (2008/03/12)
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
Jaeger, David A.,Shinozaki, Hiraku,Goodson, Patricia A.
, p. 2482 - 2489 (2007/10/02)
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.