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bis(quinolin-8-olato-N,O)magnesium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67952-28-7

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67952-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67952-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,5 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67952-28:
(7*6)+(6*7)+(5*9)+(4*5)+(3*2)+(2*2)+(1*8)=167
167 % 10 = 7
So 67952-28-7 is a valid CAS Registry Number.

67952-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(8-quinolinato)magnesium(II)

1.2 Other means of identification

Product number -
Other names Magnesium, bis(8-quinolinolato-N,O)-

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:67952-28-7 SDS

67952-28-7Upstream product

67952-28-7Downstream Products

67952-28-7Relevant academic research and scientific papers

Organic light-emitting element and display apparatus

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Page/Page column 91, (2020/04/26)

Provided is an organic light-emitting element having high luminous efficiency and a long lifetime. The organic light-emitting element includes a pair of electrodes and an organic compound layer placed between the pair of electrodes, in which the organic compound layer includes an iridium complex having a benzo[f]isoquinoline of a specific structure as a ligand and a metal complex compound of a specific structure.

Design, synthesis, and antifungal evaluation of 8-hydroxyquinoline metal complexes against phytopathogenic fungi

Chen, Yong-Jia,Liu, Ying-Qian,Ma, Kun-Yuan,Shang, Xiao-Fei,Sun, Yu,Wang, Ren-Xuan,Wang, Yu-Ling,Yin, Xiao-Dan,Zhao, Zhong-Min,Zhu, Jia-Kai

, p. 11096 - 11104 (2020/11/09)

Phytopathogenic fungal infections have become a major threat to agricultural production, food security, and human health globally, and novel antifungal agents with simple chemical scaffolds and high efficiency are needed. In this study, we designed and synthesized 38 8-hydroxyquinoline metal complexes and evaluated their antifungal activities. The results showed that most of the tested compounds possessed remarkable in vitro antifungal activity. Especially, compound 1e exhibited the highest antifungal potency among all target compounds, with EC50 values of 0.0940, 0.125, 2.95, and 5.96 μg/mL, respectively, against Sclerotinia sclerotiorum, Botrytis cinerea, Fusarium graminearum, and Magnaporthe oryzae. Preliminary mechanistic studies had shown that compound 1e might cause mycelial abnormalities of S. sclerotiorum, cell membrane permeability changes, leakage of cell contents, and inhibition of sclerotia formation and germination. Moreover, the results of in vivo antifungal activity of compound 1e against S. sclerotiorum showed that 1e possessed higher curative effects than that of the positive control azoxystrobin. Therefore, compound 1e is expected to be a novel leading structure for the development of new antifungal agents.

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