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[1,1'-Binaphthacene]-4,4'-dicarboxylicacid,3,3'-diethyl-1,1',2,2',3,3',4,4',6,6',11,11'-dodecahydro-3,3',10,10',12,12'-hexahydroxy-6,6',11,11'-tetraoxo-,dimethyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64040-81-9

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64040-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64040-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,4 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64040-81:
(7*6)+(6*4)+(5*0)+(4*4)+(3*0)+(2*8)+(1*1)=99
99 % 10 = 9
So 64040-81-9 is a valid CAS Registry Number.

64040-81-9SDS

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 bi(7-deoxyaklavinon-7-yl)

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 -
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More Details:64040-81-9 SDS

64040-81-9Relevant academic research and scientific papers

Spectroscopic and Kinetic Evidence for the Tautomer of 7-deoxyalklavinone as an Intermediate in the Reductive Coupling of Aclacinomycin A

Kleyer, Don L.,Gaudiano, Giorgio,Koch, Tad H.

, p. 1105 - 1109 (1984)

Reduction of aclacinomycin A (7) with an excess of dl-bi(3,5,5-trimethyl-2-oxomorpholin-3-yl) (11) in Trizma-buffered methanol solvent in the absence of oxygen gave 7-deoxyalkavinone (8), bi(7-deoxyalkavinon-7-yl) (9), 5,6-dihydro-3,5,5-trimethyl-1,4-oxazin-2-one (12), and 3,5,5-trimethyl-2-oxomorpholine (13).The reducing agent was 3,5,5-trimethyl-2-oxomorpholin-3-yl (5) resulting from bond homolysis of 11.The relative yields of 8 and 9 were a function of the initial concentrations of 7 and 11 and the reaction time.The semiquinone 15 of 7 was observed as anintermediate by EPR spectroscopy.Uv-visible spectroscopic monitoring revealed the formation of the tautomer 14 of 7-deoxyalklavinone as a second intermediate in the formation of both 8 and 9.The tautomer showed absorption at 350 and 548 nm.Reaction of 9 with 11 resulted in reductive cleavage of 9 to 8 and disproportionation of 11 to 12 and 13.The mechanism proposed for the reduction of 7 is shown in Scheme III and includes protonation of 14 to give 8 and coupling of 14 followed by oxidation with 12 to give 9.The decay of the tautomer absorption followed mixed kinetics, first and second order in 14.Nonlinear least-squares analysis of the decay gave a pseudo-first-order rate constant for protonation equal to 3.36x10-3s-1 and a second-order rate constant for coupling equal to approximately 180 M-1s-1.The tautomer 14 of 7-deoxyalklavinone is protonated in buffered methanol 15 times slower than the tautomer 6 of 7-deoxydaunomycinone, thus allowing the coupling reaction to take place.The difference in reactivity of the tautomers may be relevant to the tumorresponse and toxicity of the two anthracyclines.

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