105955-04-2

Basic information

• Product Name: 3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenyl-
• Synonyms: 5-hydroxy-1-(4-hydroxy-phenyl)-7-phenyl-heptan-3-one
• CAS NO: 105955-04-2
• Molecular Formula: C19H22O3
• Molecular Weight: 298.382
• Mol File: 105955-04-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenyl-(105955-04-2)
• EPA Substance Registry System: 3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenyl-(105955-04-2)

Safety Data

• Hazardous Substances Data: 105955-04-2(Hazardous Substances Data)

Usage

Description

3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenylis a chemical compound with a molecular formula of C18H18O3. It is a phenolic compound with antioxidant properties and is found in certain plants. 3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenylis characterized by the presence of a ketone group and two hydroxyl groups attached to a phenyl ring, which contribute to its unique chemical properties and potential applications.

Uses

Used in Pharmaceutical Industry:
3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenylis used as a pharmaceutical agent for its antioxidant properties. Its ability to neutralize free radicals and protect cells from oxidative damage makes it a promising candidate for the development of drugs targeting various diseases and conditions related to oxidative stress.
Used in Cosmetics Industry:
In the cosmetics industry, 3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenylis used as an active ingredient in skincare products. Its antioxidant properties help to protect the skin from environmental stressors and promote a healthy, youthful appearance.
Used in Food Production:
3-Heptanone, 5-hydroxy-1-(4-hydroxyphenyl)-7-phenylis used in the food production industry as a natural preservative. Its antioxidant properties help to extend the shelf life of food products by preventing the oxidation of fats and oils, thus maintaining the quality and freshness of the products.

Upstream product

• 1158558-75-8 3-(4-hydroxy-phenethyl)-5-phenethyl-4,5-dihydro-isoxazole 
• 5471-51-2 4-(4-hydroxyphenyl)-2-oxobutane 
• 7074-09-1 4-[4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]butan-2-one 
• 256946-31-3 5-hydroxy-7-phenyl-1-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-heptan-3-one 
• 1062083-17-3 1-(4-hydroxyphenyl)-7-phenyl-(6E)-6-hepten-5-ol-3-one 

Downstream Products

• 1062083-22-0 1-(4 hydroxyphenyl)-7-phenyl-hept-4-en-3-one 

Relevant articles and documents

Synthesis and biological evaluation of phenolic 4,5-dihydroisoxazoles and 3-hydroxy ketones as estrogen receptor α and β agonists

In this work, 52 diphenyl-4,5-dihydroisoxazoles and -3-hydroxy ketones were prepared and their estrogen receptor α (ERα) and estrogen receptor β (ERβ) activities were explored in order to systematize and maximize their biological activity. The biological

Synthesis and digestibility inhibition of diarylheptanoids: Structure- activity relationship

(±)-5-Hydroxy-1,7-bis-(4'-hydroxyphenyl)-3-heptanone (2a), (±)5- hydroxyl-1-(4'-hydroxyphenyl)-7-phenyl-3-heptanone (2b), (±)-5-hydroxy-7- (4'-hydroxyphenyl)-1-phenyl-3-heptanone (2c), and (±)-5-hydroxy-1,7- bis(phenyl)-3-heptanone (2d) have been synthesized to study the structure- activity relationship regarding digestibility inhibition in vitro in cow rumen fluid. The activities were compared with the activity of chiral (S)-2a and its glucoside platyphylloside (1), isolated from Betula pendula. Compound 2a was slightly less active, 2b and 2c were more active, and 2d was less active than (S)-2a and platyphylloside.