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879583-48-9

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879583-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879583-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,5,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 879583-48:
(8*8)+(7*7)+(6*9)+(5*5)+(4*8)+(3*3)+(2*4)+(1*8)=249
249 % 10 = 9
So 879583-48-9 is a valid CAS Registry Number.

879583-48-9SDS

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 diethyl (3-(4-methoxyphenyl)allyl)phosphonate

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:879583-48-9 SDS

879583-48-9Relevant articles and documents

Finding more active antioxidants and cancer chemoprevention agents by elongating the conjugated links of resveratrol

Tang, Jiang-Jiang,Fan, Gui-Juan,Dai, Fang,Ding, De-Jun,Wang, Qi,Lu, Dong-Liang,Li, Ran-Ran,Li, Xiu-Zhuang,Hu, Li-Mei,Jin, Xiao-Ling,Zhou, Bo

, p. 1447 - 1457 (2012/05/05)

Resveratrol is the subject of intense research as a natural antioxidant and cancer chemopreventive agent. There has been a great deal of interest and excitement in understanding its action mechanism and developing analogs with antioxidant and cancer chemoprevention activities superior to that of the parent compound in the past decade. This work delineates that elongation of the conjugated links is an important strategy to improve the antioxidant activity of resveratrol analogs, including hydrogen atom- or electron-donating ability in homogeneous solutions and antihemolysis activity in heterogeneous media. More importantly, C3, a triene bearing 4,4′-dihydroxy groups, surfaced as an important lead compound displaying remarkably increased antioxidant, cytotoxic, and apoptosis-inducing activities compared with resveratrol.

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