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82759-10-2

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82759-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82759-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82759-10:
(7*8)+(6*2)+(5*7)+(4*5)+(3*9)+(2*1)+(1*0)=152
152 % 10 = 2
So 82759-10-2 is a valid CAS Registry Number.

82759-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-5-(4-methylpiperazin-1-yl)-2-nitroaniline

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:82759-10-2 SDS

82759-10-2Relevant articles and documents

Design and synthesis of benzothiazole schiff bases of potential antitumor activity

Al-Harthy, Thuraya,Abdel-Jalil, Raid,Zoghaib, Wajdi,Pflüger, Maren,Hofmann, Elisabeth,Hundsberger, Harald

, p. 1282 - 1292 (2016/07/26)

In an attempt to develop a new class of selective antitumor agents, a novel series of benzothiazole derivatives was prepared via the condensation of 5-fluoro-6-(4-methylpiperazin-1-yl)benzo[d]thiazol-2- Amine with aromatic aldehydes. The preliminary bioassay reveals that (4-fluorobenzylidene)-[5-fluoro-6-(4-methylpiperazin-1-yl)-benzothiazol-2-yl]- Amine show specific anticancer cytotoxicity.

PYRAZOLYLBENZIMIDAZOLE DERIVATIVES, COMPOSITIONS CONTAINING THEM AND USE THEREOF

-

Page/Page column 18, (2009/08/16)

The disclosure relates to compounds of formula (I): wherein R1, R2, R3, R4, and R5 are as defined in the disclosure, to the compositions containing them and to the use thereof as medicaments, in particular as anticancer agents. The disclosure also relates to the process for preparing the compounds of formula (I) and to reaction intermediates.

Synthesis of new 2-ferrocenyl-5-fluoro-6-(4-substituted-1-piperazinyl)-1H- benzimidazoles of potential biological interest

Abdel-Jalil, Raid J.,Voelter, Wolfgang

, p. 67 - 71 (2007/10/03)

New substituted 2-ferrocenylbenzimidazole derivatives are prepared by the oxidation of corresponding Schiffs bases in situ, generated from corresponding 1,2-diamino-4-fluoro-5-(1-piperazinyl)benzenes and 2-ferrocenecarboxaldehyde using nitrobenzene.

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