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9,10-Anthracenedione, 1,8-bis[[(4-methylphenyl)sulfonyl]oxy]-, also known as 1,8-bis(4-methylbenzenesulfonyloxy)anthraquinone, is a complex organic compound with the molecular formula C22H18O8S2. It is a derivative of anthraquinone, characterized by the presence of two sulfonyl groups attached to the 1 and 8 positions of the anthraquinone core. The sulfonyl groups are derived from 4-methylbenzenesulfonic acid, which contributes to the compound's chemical structure and properties. 9,10-Anthracenedione, 1,8-bis[[(4-methylphenyl)sulfonyl]oxy]- is often used in the synthesis of dyes and other organic compounds due to its reactive sulfonyl groups, which can participate in various chemical reactions.

65771-84-8

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65771-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65771-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,7 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65771-84:
(7*6)+(6*5)+(5*7)+(4*7)+(3*1)+(2*8)+(1*4)=158
158 % 10 = 8
So 65771-84-8 is a valid CAS Registry Number.

65771-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [8-(4-methylphenyl)sulfonyloxy-9,10-dioxoanthracen-1-yl] 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 1,8-bis(tosyloxy)-9,10-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:65771-84-8 SDS

65771-84-8Downstream Products

65771-84-8Relevant academic research and scientific papers

Potentiometric and spectrophotometric studies of the equilibria between silver(i) ion and crown ethers containing chromophore substituents in propylene carbonate

Ossowski, Tadcusz,Kira, Jaromir,Rogowska, Dorota,Warmke, Hanna,Mlodzianowski, Janusz

, p. 689 - 696 (2000)

Potentiometric and UV-spectrophotometric methods have been used to study the coordination properties of crown ethers and their derivatives containing 9,10-dioxo-l-anthryl, 8-hydroxy-9,10-dioxo-l-anthryl and 8-tosyloxy-9,10dioxo-1-anthryl substituents with respect to the silver(i) ion in propylene carbonate. It was found that unsubstituted crown ligands were capable of forming two types of complex ion. The silver(i) ion can enter the macrocycle cavity forming 1:1 complexes or can coordinate externally to the nitrogen atom of a ligand as occurs for typical complexes of silver(i) with nitrogen ligands. This results in Ag(crown)2+ complexes. Introduction of chromophore groups allows investigation of the mechanism of AgL+ and AgL2+ complex formation by spectrophotometric methods. Attaching a bulky chromophore to the nitrogen atom of the aza-crown makes the formation of the AgL2+ complexes formonoaza-crown-15 strongly restricted or impossible. For 13-(9,10-dioxo-l-anthryl)-l,4,7,10-tetraoxa-13azacyclopentadecane (AjlSCSAQN) the presence of only one substituent leads to an increase in the stability of the external complex (AgL2) and the formation of other complex structures Ag2L32+ and Ag3L23+. The Royal Society of Chemistry 2000.

1,8-Substituted anthraquinones, anthrones and bianthrones as potential non-azole leads against fungal infections

Jalab, Murhaf,Critchley, Megan E.,Taylor, Charlotte M.,Lawrence, Clare L.,Smith, Robert B.

, (2019/08/01)

The synthesis of a variety of 1,8-substituted anthraquinones, anthrones and bianthrones and their potential as antifungal agents is evaluated. Preliminary screening against Schizosaccharomyces pombe (S. pombe), a fission yeast, and Saccharomyces cerevisiae (S. cerevisiae), a budding yeast, is reported. Both these yeast species demonstrate close homologue to a number of pathogenic fungi.

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