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5,12-Naphthacenedione, 11-chloro-2,6-dihydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83352-52-7

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83352-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83352-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83352-52:
(7*8)+(6*3)+(5*3)+(4*5)+(3*2)+(2*5)+(1*2)=127
127 % 10 = 7
So 83352-52-7 is a valid CAS Registry Number.

83352-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-chloro-2,6-dihydroxytetracene-5,12-dione

1.2 Other means of identification

Product number -
Other names 5,12-Naphthacenedione,11-chloro-2,6-dihydroxy

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:83352-52-7 SDS

83352-52-7Downstream Products

83352-52-7Relevant academic research and scientific papers

ANTHRACYCLINES. CYCLOADDITIONS OF 9-CHLORO-10-HYDROXY-1,4-ANTHRAQUINONE WITH VARIOUS BUTA-1,3-DIENES

Agarwal, Nand L.,Sheeren, Hans W.

, p. 1057 - 1060 (1982)

The Diels-Alder type cycloaddition of several substituted buta-1,3-dienes with 9-chloro-10-hydroxy-1,4-anthraquinone (10) affords an efficient, regiospecific access in two steps to tetracyclic ketones (12-14) which have been investigated as intermediates for the synthesis of anthracycline derivatives.Butadienes with a less asymmetric ?-electron distribution than 9 give lower regiospecificity in cycloadditions with 10.Depending on the substituents in the used butadiene, the obtained cycloadducts are transformed under the reaction circumstances into the aromatized products (15-20).

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