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(5R)-5-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1-phenylheptan-3-one is a chalcone derivative with a molecular structure that includes a heptan-3-one backbone, a hydroxy group, and a phenyl ring. It has potential pharmacological properties due to the presence of the hydroxy and methoxy groups, which may contribute to antioxidative and anti-inflammatory activities.
Used in Pharmaceutical Industry:
(5R)-5-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1-phenylheptan-3-one is used as a potential therapeutic agent for treating various diseases, including cancer, diabetes, and neurodegenerative disorders, due to its potential pharmacological properties and the presence of hydroxy and methoxy groups that may contribute to antioxidative and anti-inflammatory activities.
Used in Research and Development:
(5R)-5-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1-phenylheptan-3-one is used as a subject of investigation and characterization in scientific studies to further explore its specific properties and potential uses in treating various diseases.

68622-73-1

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68622-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68622-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,2 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68622-73:
(7*6)+(6*8)+(5*6)+(4*2)+(3*2)+(2*7)+(1*3)=151
151 % 10 = 1
So 68622-73-1 is a valid CAS Registry Number.

68622-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5R)-5-hydroxy-7-(4''-hydroxy-3''-methoxyphenyl)-1-phenyl-3-heptanone

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

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More Details:68622-73-1 SDS

68622-73-1Upstream product

68622-73-1Downstream Products

68622-73-1Relevant 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

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