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2,7-Dihydroxy-1,4-naphthoquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31039-63-1

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31039-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31039-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31039-63:
(7*3)+(6*1)+(5*0)+(4*3)+(3*9)+(2*6)+(1*3)=81
81 % 10 = 1
So 31039-63-1 is a valid CAS Registry Number.

31039-63-1SDS

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 4,7-dihydroxynaphthalene-1,2-dione

1.2 Other means of identification

Product number -
Other names 2,7-dihydroxynapthalene-1,4-dione

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:31039-63-1 SDS

31039-63-1Downstream Products

31039-63-1Relevant academic research and scientific papers

The first enantioselective total synthesis of lantalucratin C and determination of its absolute configuration

Ogata, Tokutaro,Tanaka, Manami,Ishigaki, Momoe,Shimizu, Maki,Nishiuchi, Arisa,Inamoto, Kiyofumi,Kimachi, Tetsutaro

, p. 6672 - 6680 (2015)

Described here is the first enantioselective total synthesis of lantalucratin C, which was isolated from the rainforest plant Lantana involucrata, and which possesses anti-tumor activity. The OH group on the aromatic ring was systematically introduced by

Palladium(II)-Catalyzed Reaction of Lawsones and Propargyl Carbonates: Construction of 2,3-Furanonaphthoquinones and Evaluation as Potential Indoleamine 2,3-Dioxygenase Inhibitors

Feng, Xi,Qiu, Xiaqiu,Huang, Huidan,Wang, Jubo,Xu, Xi,Xu, Pengfei,Ge, Ruijia,Liu, Xiaojin,Li, Zhiyu,Bian, Jinlei

, p. 8003 - 8010 (2018/06/22)

An efficient reaction utilizing propargyl carbonates through Claisen rearrangement to synthesize furanonaphthoquinones is described. The remarkable transformation exhibits excellent functional group tolerance, affording the target furanonaphthoquinones in

Unusual, chemoselective etherification of 2-hydroxy-1,4-naphthoquinone derivatives utilizing alkoxymethyl chlorides: Scope, mechanism and application to the synthesis of biologically active natural product (±)-lantalucratin C

Ogata, Tokutaro,Yoshida, Tomoyo,Shimizu, Maki,Tanaka, Manami,Fukuhara, Chie,Ishii, Junko,Nishiuchi, Arisa,Inamoto, Kiyofumi,Kimachi, Tetsutaro

, p. 1423 - 1432 (2017/02/15)

A novel etherification of 2-hydroxy-1,4-naphthoquinone derivatives with alkoxyalkyl chlorides and hydride bases is described. Precise study of the conditions and substrate scope suggested that the reaction occurs specifically in the molecule having a 2-hydroxy-1,4-benzoquinone skeleton. A chemoselective O-methylation reaction was achieved to afford a synthetically important intermediate, which offered easy access to a natural product possessing anti-tumor activity.

Fused quinonic compounds

-

, (2014/02/15)

A compound having the formula (I): for use in treating disease; a composition comprising said fused quinonic compound of formula (I) and at least one pharmaceutically acceptable carrier; as well as a method of modulating a Janus Kinase-Signal Transduction

FUSED QUINONIC COMPOUNDS

-

Page/Page column 49; 50, (2014/02/16)

A compound having the formula (I), for use in treating a disease; a composition comprising said fused quinonic compound of formula (I) and at least one pharmaceutically acceptable carrier; as well as a method of modulating a Janus Kinase-Signal Transducti

Biomimetic synthesis of antimalarial naphthoquinones

Malerich, Jeremiah P.,Maimone, Thomas J.,Elliott, Gregory I.,Trauner, Dirk

, p. 6276 - 6283 (2007/10/03)

The total synthesis of naphthoquinone natural products isolated from the Bignoniaceae plant family is described. Pinnatal, isopinnatal, sterekunthals A and B, pyranokunthones A and B, and anthrakunthone have been prepared along the lines of a biosynthetic

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.

Reactivity of potassium superoxide in heterogeneous phase: Oxidation of naphthalenediols and hydroxylated naphthoquinones

De Min,Croux,Tournaire,Hocquaux,Jacquet,Oliveros,Maurette

, p. 1869 - 1882 (2007/10/02)

Oxidation of dihydroxynaphthalenes by potassium superoxide (KO2) in heterogeneous aprotic media yields mono- or dihydroxynaphthoquinones, depending on the relative position of the hydroxy groups on the naphthalene moiety. The reaction proceeds mainly at the solid-liquid interface and naphthoquinones can be obtained with good yields.

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