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(4E)-7-(4-hydroxy-3-methoxyphenyl)-1-phenylhept-4-en-3-one is an organic compound with a complex molecular structure, consisting of a heptenone skeleton with a phenyl group attached at the 1-position and a hydroxy-3-methoxyphenyl group at the 7-position. It is classified as a chalcone, a type of natural phenol, commonly found in various plants and fruits. (4E)-7-(4-hydroxy-3-methoxyphenyl)-1-phenylhept-4-en-3-one exhibits antioxidant, anti-inflammatory, and anti-cancer properties, making it a subject of interest in pharmaceutical and medical research.

79559-60-7

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79559-60-7 Usage

Uses

Used in Pharmaceutical and Medical Research:
(4E)-7-(4-hydroxy-3-methoxyphenyl)-1-phenylhept-4-en-3-one is used as a pharmaceutical and medical research compound for its antioxidant, anti-inflammatory, and anti-cancer properties. Its potential therapeutic applications are being explored for the development of new treatments and interventions.
Used in Flavoring and Fragrance Industry:
(4E)-7-(4-hydroxy-3-methoxyphenyl)-1-phenylhept-4-en-3-one is used as a flavoring and fragrance agent in the food and cosmetic industries. Its unique chemical structure contributes to the sensory characteristics of various products, enhancing their appeal to consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 79559-60-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,5 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79559-60:
(7*7)+(6*9)+(5*5)+(4*5)+(3*9)+(2*6)+(1*0)=187
187 % 10 = 7
So 79559-60-7 is a valid CAS Registry Number.

79559-60-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(4'-hydroxy-3'-methoxyphenyl)-1-phenyl-4E-heptene-3-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:79559-60-7 SDS

79559-60-7Downstream Products

79559-60-7Relevant academic research and scientific papers

Synthesis of Bioactive Diarylheptanoids from Alpinia officinarum and Their Mechanism of Action for Anticancer Properties in Breast Cancer Cells

Gamre, Sunita,Tyagi, Mrityunjay,Chatterjee, Sucheta,Patro, Birija S.,Chattopadhyay, Subrata,Goswami, Dibakar

, p. 352 - 363 (2021/03/01)

An efficient synthesis of the Alpinia officinarum-derived diarylheptanoids, viz., enantiomers of a β-hydroxyketone (1) and an α,β-unsaturated ketone (2) was developed starting from commercially available eugenol. Among these, compound 2 showed a superior

NEW METHODS AND REAGENTS IN ORGANIC SYNTHESIS. 47. A GENERAL, EFFICIENT, AND CONVENIENT SYNTHESIS OF DIARYLHEPTANOIDS

Kato, Nobuharu,Hamada, Yasumasa,Shioiri, Takayuki

, p. 3323 - 3326 (2007/10/02)

An efficient synthesis of physiologically interesting diarylheptanoids has been carried out through direct C-acylation using diethyl phosphorocyanidate (DEPC) followed by Grignard reactions with aldehydes.Keywords - diarylheptanoid; C-acylation; diethyl p

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