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2-Hydroxy-3-methoxy-1,4-naphthalenedione, also known as juglone, is a chemical compound derived from the breakdown of the natural pigment lawsone. It is a polyphenolic compound with a molecular formula of C11H8O4 and a molecular weight of 200.18 g/mol. Juglone is a yellow crystalline solid that is soluble in water, ethanol, and other organic solvents. It is commonly found in the heartwood and bark of the black walnut tree (Juglans nigra) and has been identified in several other plant species as well. 2-Hydroxy-3-methoxy-1,4-naphthalenedione exhibits various biological activities, including antifungal, antibacterial, and cytotoxic properties. Due to its potential toxic effects on certain plants, juglone has been used as a natural herbicide to control the growth of unwanted vegetation. Additionally, it has been studied for its potential applications in the pharmaceutical and cosmetic industries.

5257-83-0

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5257-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5257-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5257-83:
(6*5)+(5*2)+(4*5)+(3*7)+(2*8)+(1*3)=100
100 % 10 = 0
So 5257-83-0 is a valid CAS Registry Number.

5257-83-0SDS

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-hydroxy-3-methoxynaphthalene-1,2-dione

1.2 Other means of identification

Product number -
Other names 1,4-Naphthalenedione,2-hydroxy-3-methoxy

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:5257-83-0 SDS

5257-83-0Downstream Products

5257-83-0Relevant academic research and scientific papers

Expedient synthesis of 3-hydroxyisoquinolines and 2-hydroxy-1,4- naphthoquinones via one-pot aryne acyl-alkylation/condensation

Allan, Kevin M.,Hong, Boram D.,Stoltz, Brian M.

supporting information; experimental part, p. 4960 - 4964 (2010/02/15)

A convenient method is disclosed for the synthesis of both 3-hydroxyisoquinolines and 2-hydroxy-1,4-naphthoquinones from β-ketoesters using a one-pot aryne acyl-alkylation/condensation procedure. When performed in conjunction with a one-step method for the synthesis of the β-ketoester substrates, this method provides a new route to these polyaromatic structures in only two steps from commercially available carboxylic acid starting materials. The utility of this approach is demonstrated in the synthesis of the atropisomeric P,N-ligand, QUINAP. The Royal Society of Chemistry 2009.

Method for dyeing keratinous fibres using a monohydroxyindole or dihydroxyindole and a non-oxidizing aromatic carbonyl derivative and dyeing agent

-

, (2008/06/13)

The present invention relates to a method for dyeing keratinous fibers, characterized in that the following are applied to the fibers: a) a composition (A) containing, in a medium appropriate for dyeing, at least one monohydroxyindole or dihydroxyindole, this application being preceded or followed by the application of b) a composition (B) containing, in a medium appropriate for dyeing, at least one aromatic carbonyl derivative chosen from hydroxyacetophenones, hydroxybenzophenones, 2-hydroxy-1,4-benzoquinones, hydroxy-1,4-naphthoquinones,amino-1,4-naphthoquinones,hydroxy-9,10-anthraquinones and amino-9,10-anthraquinones. It also relates to the dyeing agents for carrying it out.

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