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7-Deoxydaunorubicin aglycone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59367-18-9

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59367-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59367-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,6 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59367-18:
(7*5)+(6*9)+(5*3)+(4*6)+(3*7)+(2*1)+(1*8)=159
159 % 10 = 9
So 59367-18-9 is a valid CAS Registry Number.

59367-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-7-deoxy-daunomyvinone

1.2 Other means of identification

Product number -
Other names 7-Deoxydaunomycicon

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:59367-18-9 SDS

59367-18-9Downstream Products

59367-18-9Relevant academic research and scientific papers

REGIOSELECTIVE SYNTHESE VON DAUNOMYCINON UND γ-RHODOMYCINON

Braun, Manfred

, p. 3871 - 3874 (1980)

Synthesis of daunomycinone (2) and γ-rhodomycinone (3) by regioselective addition of the Grignard reagents 9b and 9d to the anhydride 4.

Anthracyclines. Part 1. The Synthesis of Racemic Daunomycinone and Some Related Tetrahydronaphthacenequinones

Broadhurst, Michael J.,Hassall, Cedric H.

, p. 2227 - 2238 (2007/10/02)

New tetrahydronaphthacenequinones, which are related in structure to the aglycones of the antitumor drugs adriamycin and daunomycin, have been synthesised.Racemic daunomycinone has been prepared by a new, mild procedure utilising a phthalide intermediate

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