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5-Hydroxy-2,7-dimethoxynaphthalene-1,4-dione is a naturally occurring organic compound belonging to the class of naphthalene derivatives. It is characterized by a naphthalene core with a hydroxyl group at the 5th position, and two methoxy groups at the 2nd and 7th positions. The compound also features a 1,4-dione functional group, which consists of two carbonyl groups (C=O) separated by a single carbon atom. This molecule is known for its potential biological activities and can be found in various plants, contributing to their medicinal properties. The chemical structure of 5-hydroxy-2,7-dimethoxynaphthalene-1,4-dione is significant in the field of natural product chemistry and pharmacology, as it may possess antioxidant, anti-inflammatory, or other therapeutic effects.

5518-91-2

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5518-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5518-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,1 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5518-91:
(6*5)+(5*5)+(4*1)+(3*8)+(2*9)+(1*1)=102
102 % 10 = 2
So 5518-91-2 is a valid CAS Registry Number.

5518-91-2Relevant academic research and scientific papers

A New Method for Thiomethylation of Hydroxy-1,4-naphthoquinones with N -Acetyl- l -cysteine; First Synthesis of Fibrostatins B, C, and D

Sabutskii, Yuri E.,Polonik, Sergey G.,Denisenko, Vladimir A.,Dmitrenok, Pavel S.

, p. 2763 - 2770 (2015/02/19)

A series of N-acetyl-S-[(3-hydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)methyl]-l-cysteine conjugates were obtained in good yields by acid-catalyzed condensation of substituted 2-hydroxy-1,4-naphthoquinones with N-acetyl-l-cysteine and paraformaldehyde. Based on this reaction, a first synthesis of fibrostatins B, C, and D was developed.

REACTIONS OF KETENE ACETALS-14; THE USE OF SIMPLE MIXED VINYLKETENE ACETALS IN THE ANNULATION OF QUINONES

Savard, Jacques,Brassard, Paul

, p. 3455 - 3464 (2007/10/02)

α,β- and β,γ-unsaturated esters can be converted by strong base and chlorotrimethylsilane to the corresponding mixed vinylketene acetals which are shown to be particularly useful and generally applicable reagents for the regiospecific annulation of halogenoquinones.The reaction proceeds readily with a variety of substrates including benzoquinones.

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