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Benzamide, N-(9,10-dihydro-9,10-dioxo-2-anthracenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52869-18-8

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52869-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52869-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,6 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52869-18:
(7*5)+(6*2)+(5*8)+(4*6)+(3*9)+(2*1)+(1*8)=148
148 % 10 = 8
So 52869-18-8 is a valid CAS Registry Number.

52869-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9,10-dioxoanthracen-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names 2-Benzoylamino-anthrachinon

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:52869-18-8 SDS

52869-18-8Relevant academic research and scientific papers

Selective colorimetric sensor for cyanide anion based on 1-hydroxyanthraquinone

Gromov, Sergey P.,Klimenko, Lyubov S.,Korchagin, Denis V.,Kudrevatykh, Alexandra A.,Martyanov, Timofey P.,Sulimenkov, Ilia V.,Ushakov, Evgeny N.,Vasil'ev, Sergey G.

, (2021/07/19)

The article addresses the synthesis, structure and properties of 2-benzoylamino-1-hydroxyanthraquinone (1a), which can function as a selective colorimetric sensor for the cyanide anion in aqueous media. Compound 1a was prepared in two simple steps in good

A palladium-catalyzed carbonylation approach to acid chloride synthesis

Quesnel, Jeffrey S.,Arndtsen, Bruce A.

supporting information, p. 16841 - 16844 (2013/12/04)

We describe a new approach to acid chloride synthesis via the palladium-catalyzed carbonylation of aryl iodides. The combination of sterically encumbered phosphines (PtBu3) and CO coordination has been found to facilitate the rapid carbonylation of aryl iodides into acid chlorides via reductive elimination from (tBu3P)(CO) Pd(COAr)Cl. The formation of acid chlorides can also be exploited to perform traditional aminocarbonylation reactions under exceptionally mild conditions (ambient temperature and pressure), and with a range of weakly nucleophilic substrates.

Relation between the basicity and the rate constant for the acylation of aminoanthraquinones

Yakovlev, Yu. Yu.,Nurmukhametov, R. N.,Barashkov, N. N.,Klimenko, V. G.

, p. 110 - 111 (2007/10/02)

The basicity constants of aminoanthraquinones and diaminoanthraquinones and the rate constants for their acylation of benzoyl chloride were determined.

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