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91441-23-5

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91441-23-5 Usage

Uses

Antineoplastic.

Check Digit Verification of cas no

The CAS Registry Mumber 91441-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,4 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91441-23:
(7*9)+(6*1)+(5*4)+(4*4)+(3*1)+(2*2)+(1*3)=115
115 % 10 = 5
So 91441-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H25N5O4/c22-6-1-7-24-12-2-3-13-17-16(12)21(30)19-15(29)5-4-14(28)18(19)20(17)25-26(13)10-8-23-9-11-27/h2-5,23-24,27-29H,1,6-11,22H2

91441-23-5SDS

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 5-[(3-Aminopropyl)amino]-7,10-dihydroxy-2-{2-[(2-hydroxyethyl)ami no]ethyl}dibenzo[cd,g]indazol-6(2H)-one

1.2 Other means of identification

Product number -
Other names 5-<(2'-Methylaminophenyl)-thio>-4-brom-2-phenyl-3-pyridazinon

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:91441-23-5 SDS

91441-23-5Downstream Products

91441-23-5Relevant academic research and scientific papers

Anticancer anthrapyrazoles. Improved syntheses of clinical agents CI-937, CI-941, and piroxantrone hydrochloride

Beylin,Colbry,Goel,Haky,Johnson,Johnson,Kanter,Leeds,Leja,Lewis,Rithner,Showalter,Sercel,Turner,Uhlendorf

, p. 85 - 96 (2007/10/02)

Improved processes for the synthesis of bulk quantities of the anthrapyrazole clinical agents CI-937, CI-941, and piroxantrone hydrochloride are reported. Reported also are detailed analytical and spectroscopic data for these agents and intermediates of t

Anthrapyrazole anticancer agents. Synthesis and structure-activity relationships against murine leukemias

Showalter,Johnson,Hoftiezer,Turner,Werbel,Leopold,Shillis,Jackson,Elslager

, p. 121 - 131 (2007/10/02)

Chromophore modification of the anthracenediones related to mitoxantrone in an attempt to provide agents with diminished or no cardiotoxicity has resulted in a novel class of DNA binders, the anthrapyrazoles. Their synthesis was carried out by a two-stage

Process for preparing substituted anthra[1,9-cd]pyrazol-6(2H)-ones

-

, (2008/06/13)

An improved process for making anthra[1,9-cd]pyrazol-6(2H)-ones from 1,4-dichloro-5,8-disubstituted-9,10-anthracenediones and a hydrazine is disclosed. The compounds produced have antibacterial, antifungal, antileukaemic, and antitumor activity.

Antimicrobial substituted anthra[1,9-cd]pyrazol-6(2H)-ones

-

, (2008/06/13)

Substituted anthra[1,9-cd]pyrazol-6(2H-ones have antimicrobial activity. Methods for their preparation, use and pharmaceutical compositions are disclosed.

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