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476-37-9

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476-37-9 Usage

Derivative of

naphthalenedione

Sources

found in the leaves, roots, and bark of the walnut tree and other plant species

Properties

antioxidant, antimicrobial, and anticancer

Uses

production of dyes, natural pesticide, potential allelopathic agent, possible therapeutic applications for certain skin diseases and medical research.

Check Digit Verification of cas no

The CAS Registry Mumber 476-37-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 476-37:
(5*4)+(4*7)+(3*6)+(2*3)+(1*7)=79
79 % 10 = 9
So 476-37-9 is a valid CAS Registry Number.

476-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,5,6,7,8-hexahydroxynaphthalene-2,3-dione

1.2 Other means of identification

Product number -
Other names Hexahydroxy-1,4-naphthalenedione

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:476-37-9 SDS

476-37-9Downstream Products

476-37-9Relevant articles and documents

Simple preparative synthesis of spinochrome E, a pigment from sea urchins of the genus Echinothrix

Borisova,Anufriev

, p. 202 - 204 (2012)

A preparative synthesis of spinochrome E (2,3,5,6,7,8-hexahydroxy-1,4- naphthoquinone, 1), a metabolite of sea urchins of the genus Echinothrix, is proposed starting from 2,3-dichloro-6,7-diethoxynaphthazarine (4) with simultaneous substitution of the Cl atoms by hydroxyl- and nitro-groups, reduction of the latter, and subsequent removal of alkoxy groups and hydrolysis of the amine in the resulting 3-amino-2-hydroxy-6,7-diethoxynaphthazarine (6).

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