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9,10-Anthracenedione, 1,3,6,8-tetrahydro-2-(1-methoxyhexyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28254-23-1

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28254-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28254-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,5 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28254-23:
(7*2)+(6*8)+(5*2)+(4*5)+(3*4)+(2*2)+(1*3)=111
111 % 10 = 1
So 28254-23-1 is a valid CAS Registry Number.

28254-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1'-O-methylaverantin

1.2 Other means of identification

Product number -
Other names 2-(1-methoxy-hexyl)-1,3,6,8-tetrahydroxy-anthraquinone

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:28254-23-1 SDS

28254-23-1Upstream product

28254-23-1Downstream Products

28254-23-1Relevant academic research and scientific papers

Quinofuracins A-E, produced by the fungus staphylotrichum boninense PF1444, show p53-dependent growth suppression

Tatsuda, Daisuke,Momose, Isao,Someno, Tetsuya,Sawa, Ryuichi,Kubota, Yumiko,Iijima, Masatomi,Kunisada, Takao,Watanabe, Takumi,Shibasaki, Masakatsu,Nomoto, Akio

, p. 188 - 195 (2015)

Quinofuracins A-E, novel anthraquinone derivatives containing β-d-galactofuranose that were isolated from the fungus Staphylotrichum boninense PF1444, induced p53-dependent cell death in human tumor cells. The structures of quinofuracins A-E, including absolute configurations, were elucidated by extensive spectroscopic analysis and chemical transformation studies. Quinofuracins were classified into three groups according to the aglycone moieties. 5'-Oxoaverantin was present in quinofuracins A-C, whereas averantin and versicolorin B were identified in quinofuracins D and E, respectively. These quinofuracins induced p53-dependent growth suppression in human glioblastoma LNZTA3 cells.

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