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113457-05-9

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113457-05-9 Usage

Uses

Antineoplastic (DNA topoi somerase II inhibitor) [Note—Ledoxantrone Trihy drochloride supersedes Sedoxantrone Trihydrochloride].

Check Digit Verification of cas no

The CAS Registry Mumber 113457-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,5 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113457-05:
(8*1)+(7*1)+(6*3)+(5*4)+(4*5)+(3*7)+(2*0)+(1*5)=99
99 % 10 = 9
So 113457-05-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H27N5OS.3ClH/c1-3-25(4-2)11-12-26-17-8-7-16(23-10-9-22)21-19(17)20(24-26)15-6-5-14(27)13-18(15)28-21;;;/h5-8,13,23,27H,3-4,9-12,22H2,1-2H3;3*1H

113457-05-9SDS

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 Ledoxantrone

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:113457-05-9 SDS

113457-05-9Downstream Products

113457-05-9Relevant articles and documents

Processes for the preparation of benzo(chalcogeno)(4,3,2-cd)indazoles and intermediates thereof

-

, (2008/06/13)

Improved processes for producing substituted benzo(chalcogeno)[4,3,2-cd] indazoles. The processes produce compounds in higher yields and of greater purity by using a novel sequence of acylation chemistry and easily removed protecting groups. The compounds produced have antibacterial, antifungal, antileukemic, and antitumor activity.

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