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62502-00-5

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62502-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62502-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,0 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62502-00:
(7*6)+(6*2)+(5*5)+(4*0)+(3*2)+(2*0)+(1*0)=85
85 % 10 = 5
So 62502-00-5 is a valid CAS Registry Number.

62502-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-4,3,5-trimethoxy-trans-stilbene

1.2 Other means of identification

Product number -
Other names (E)-3,4,5'-trimethoxystilben-3'-ol

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:62502-00-5 SDS

62502-00-5Relevant articles and documents

Antioxidant constituents from rhubarb: Structural requirements of stilbenes for the activity and structures of two new anthraquinone glucosides

Matsuda, Hisashi,Morikawa, Toshio,Toguchida, Iwao,Park, Ji-Young,Harima, Shoichi,Yoshikawa, Masayuki

, p. 41 - 50 (2007/10/03)

The methanolic extracts from five kinds of rhubarb were found to show scavenging activity for DPPH radical and ·O2-. Two new anthraquinone glucosides were isolated from the rhizome of Rheum undulatum L. together with two anthraquinone glucosides, a naphthalene glucoside, and 10 stilbenes. In the screening test for radical scavenging activity of rhubarb constituents, stilbenes and a naphthalene glucoside showed activity, but anthraquinones and sennosides did not. In addition, most stilbenes inhibited lipid peroxidation of erythrocyte membrane by tert-butyl hydroperoxide. Detailed examination of the scavenging effect on various related compounds suggested the following structural requirements; 1) phenolic hydroxyl groups are essential to show the activity; 2) galloyl moiety enhances the activity; 3) glucoside moiety reduces the activity; 4) dihydrostilbene derivatives maintain the scavenging activity for the DPPH radical, but they show weak activity for ·O2-. In addition, several stilbenes with both the 3-hydroxyl and 4′-methoxyl groups inhibited xanthine oxidase.

ANTI-LEUKAEMIC COMPOUNDS DERIVED FROM STILBENES IN PICEA ABIES BARK

Mannila, Erkki,Talvitie, Antti,Kolehmainen, Erkki

, p. 813 - 816 (2007/10/02)

Resveratrol was identified and isolated as a minor stilbene derivative from the bark of Picea abies.Three derivatives of resveratrol and three additional derivatives of primary stilbenes from P. abies bark were prepared.Improvement over piceatannol in ant

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