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2,5-Cyclohexadien-1-one, 4-(9-acridinylimino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106063-36-9

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106063-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106063-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,6 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106063-36:
(8*1)+(7*0)+(6*6)+(5*0)+(4*6)+(3*3)+(2*3)+(1*6)=89
89 % 10 = 9
So 106063-36-9 is a valid CAS Registry Number.

106063-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acridin-9-yliminocyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names N-9-acridinyl-1,4-benzoquinone imine

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:106063-36-9 SDS

106063-36-9Relevant academic research and scientific papers

Reactivity of Quinone Imine and Quinone Diimine Metabolites of the Antitumor Drug Amsacrine and Related Compounds to Nucleophiles

Lee, Ho H.,Palmer, Brian D.,Denny, William A.

, p. 6042 - 6047 (2007/10/02)

The quinone diimine AQDI (7) and the quinone imine AQI (10) (products of oxidative metabolism of the clinical antileukemia drug amsacrine (1)) and related compounds were prepared, and their reactions with a variety of nucleophiles were studied.Reaction of

Redox Chemistry of the 9-Anilinoacridine Class of Antitumor Agents

Jurlina, Jeffrey L.,Lindsay, Andrew,Packer, John E.,Baguley, Bruce C.,Denny, William A.

, p. 473 - 480 (2007/10/02)

9-Anilinoacridines bearing a 1'-NHR substituent on the anilino ring undergo facile, chemically reversible, two-electron oxidation to quinone diimines.The chemical and electrochemical oxidation of three groups of 9-anilinoacridines (1'-substituted derivati

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