Cas 129784-92-5,(8S,10S)-10-((2R,4S,5S,6S)-4-Amino-5-hydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-6,8,11-trihydroxy-8-(2-hydroxy-acetyl)-1-methoxy-7,8,9,10-tetrahydro-naphthacene-5,12-dione

129784-92-5

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Basic information

Product Name: (8S,10S)-10-((2R,4S,5S,6S)-4-Amino-5-hydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-6,8,11-trihydroxy-8-(2-hydroxy-acetyl)-1-methoxy-7,8,9,10-tetrahydro-naphthacene-5,12-dione
Synonyms:
CAS NO:129784-92-5
Molecular Formula:
Molecular Weight: 543.527
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (8S,10S)-10-((2R,4S,5S,6S)-4-Amino-5-hydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-6,8,11-trihydroxy-8-(2-hydroxy-acetyl)-1-methoxy-7,8,9,10-tetrahydro-naphthacene-5,12-dione(CAS DataBase Reference)
NIST Chemistry Reference: (8S,10S)-10-((2R,4S,5S,6S)-4-Amino-5-hydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-6,8,11-trihydroxy-8-(2-hydroxy-acetyl)-1-methoxy-7,8,9,10-tetrahydro-naphthacene-5,12-dione(129784-92-5)
EPA Substance Registry System: (8S,10S)-10-((2R,4S,5S,6S)-4-Amino-5-hydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-6,8,11-trihydroxy-8-(2-hydroxy-acetyl)-1-methoxy-7,8,9,10-tetrahydro-naphthacene-5,12-dione(129784-92-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 129784-92-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129784-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,8 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 129784-92:
(8*1)+(7*2)+(6*9)+(5*7)+(4*8)+(3*4)+(2*9)+(1*2)=175
175 % 10 = 5
So 129784-92-5 is a valid CAS Registry Number.

129784-92-5Upstream product

23214-92-8 doxorubicin

129784-92-5Downstream Products

129784-92-5Relevant academic research and scientific papers

An EPR Study of a Model System for the Initial Oxygen Activation Process Caused by Adriamycin-Iron System

Tachibana, Masahiko,Tero-Kubota, Shozo,Iwaizumi, Masamoto

, p. 933 - 936 (1987)

1,4-Dihydroxyanthraquinone, a model compound for Adriamycin, is reduced by Fe2+-ADP complex to generate semiquinone, while by Fe2+-phosphate complex to hydroquinone.The difference is explained in terms of the higher redox potential of the latter reducing agent.Similar reduction reactions were observed in the case of the drug.

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