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3,5-Dihydroxy-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)heptane, also known as paeonol, is a natural organic compound derived from the roots of Paeonia lactiflora, a traditional Chinese medicinal plant. It is a phenolic compound with antioxidant and anti-inflammatory properties, and has been studied for its potential therapeutic effects in managing various health conditions, including cardiovascular diseases, cancer, and neurodegenerative disorders.

408324-00-5

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408324-00-5 Usage

Uses

Used in Pharmaceutical Applications:
Paeonol is used as a therapeutic agent for managing various health conditions, such as cardiovascular diseases, cancer, and neurodegenerative disorders, due to its antioxidant and anti-inflammatory properties.
Used in Skincare Applications:
Paeonol is used as a skincare ingredient for its antioxidant and anti-aging properties, and is being investigated for its potential as a skincare ingredient.
Used in Traditional Chinese Medicine:
Paeonol is used in traditional Chinese medicine for its various health benefits and therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 408324-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,8,3,2 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 408324-00:
(8*4)+(7*0)+(6*8)+(5*3)+(4*2)+(3*4)+(2*0)+(1*0)=115
115 % 10 = 5
So 408324-00-5 is a valid CAS Registry Number.

408324-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-((3R,5R)-3,5-dihydroxy-7-(4-hydroxyphenyl)heptyl)benzene-1,2-diol

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:408324-00-5 SDS

408324-00-5Relevant academic research and scientific papers

Diarylheptanoids from Curcuma kwangsiensis and their inhibitory activity on nitric oxide production in lipopolysaccharide-activated macrophages

Li, Jun,Liao, Chun-Ru,Wei, Jun-Qi,Chen, Li-Xia,Zhao, Feng,Qiu, Feng

experimental part, p. 5363 - 5369 (2011/10/09)

Eleven diarylheptanoids (1-11) were isolated from rhizomes of Curcuma kwangsiensis, together with seven known compounds. Their structures were elucidated by 1D and 2D NMR, circular dichroism (CD), and accurate mass measurements. Inhibitory effects of the

New diarylheptanoids and diarylheptanoid glucosides from the rhizomes of Tacca chantrieri and their cytotoxic activity

Yokosuka, Akihito,Mimaki, Yoshihiro,Sakagami, Hiroshi,Sashida, Yutaka

, p. 283 - 289 (2007/10/03)

Two new diarylheptanoids (1, 2) and seven new diarylheptanoid glucosides (3-9) were isolated from the rhizomes of Tacca chantrieri. Their structures were determined by spectroscopic analysis, including 2D NMR data, and the results of hydrolytic cleavage. The absolute configurations of the 3,5-dihydroxyheptane moieties of the new diarylheptanoids were determined to be 3R and 5R by the application of the CD exciton chirality method to the corresponding 3,5-bis-p-bromobenzoyl derivatives. The cytotoxic activities of the isolated compounds and some derivatives against HL-60 human promyelocytic leukemia cells, HSC-2 human oral squamous carcinoma cells, and normal human gingival fibroblasts (HGF) are reported.

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