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152955-28-7

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152955-28-7 Usage

Type of compound

natural phenolic compound

Sources

found in various plants and foods, such as flaxseed and sesame seeds

Classification

belongs to the class of lignans

Health benefits

studied for its potential health benefits, including antioxidant and anti-inflammatory properties

Potential role

investigated for its potential role in preventing various chronic diseases, such as cardiovascular disease and cancer

Cosmetic applications

has shown potential as a natural ingredient in skincare and cosmetic products due to its anti-aging and skin-protective properties

Versatility

pinoresinol is a versatile compound with various potential health and cosmetic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 152955-28-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,9,5 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 152955-28:
(8*1)+(7*5)+(6*2)+(5*9)+(4*5)+(3*5)+(2*2)+(1*8)=147
147 % 10 = 7
So 152955-28-7 is a valid CAS Registry Number.

152955-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-hydroxy-2-phenylpropyl)-5-methoxyphenol

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:152955-28-7 SDS

152955-28-7Downstream Products

152955-28-7Relevant articles and documents

The direct synthesis of isoflavans VIA α-alkylation of phenylacetates

Versteeg, Marietjie,Bezuidenhoudt, Barend C. B.,Ferreira, Daneel

, p. 1373 - 1394 (2007/10/03)

Deprotonation of oxygenated phenylacetates and quenching of the enolates with oxygenated benzylic electrophiles, afforded 2,3-diarylpropanoates which served as precursors to the isoflavans following consecutive reduction and cyclization steps.

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