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1H-Indole-5,6-dione, commonly known as isatin, is a heterocyclic organic compound characterized by its distinctive blue color and the molecular formula C8H5NO2. It is naturally found in the plants of the Indigofera species and in human urine. Isatin exhibits versatile chemical reactivity, acting as both an oxidizing and reducing agent, and is valued for its potential pharmacological properties, including anti-cancer, anti-inflammatory, and anti-microbial activities. Additionally, it serves as a precursor for the synthesis of various pharmaceutically important compounds and dyes.

582-59-2

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582-59-2 Usage

Uses

Used in Pharmaceutical Industry:
1H-Indole-5,6-dione is used as a precursor for the synthesis of pharmaceutically important compounds due to its versatile chemical reactivity and potential pharmacological properties. It is particularly noted for its anti-cancer, anti-inflammatory, and anti-microbial activities, making it a valuable component in the development of new drugs.
Used in Dye Industry:
Isatin is used as a precursor for the synthesis of dyes, capitalizing on its distinctive blue color and ability to form intense blue complexes with metals such as tin and lead.
Used as a pH Indicator:
1H-Indole-5,6-dione is used as a pH indicator in various applications due to its ability to change color in the presence of certain pH levels, providing a visual indication of acidity or alkalinity.

Check Digit Verification of cas no

The CAS Registry Mumber 582-59-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 582-59:
(5*5)+(4*8)+(3*2)+(2*5)+(1*9)=82
82 % 10 = 2
So 582-59-2 is a valid CAS Registry Number.

582-59-2SDS

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 1H-indole-5,6-dione

1.2 Other means of identification

Product number -
Other names 5,6-indolequinone

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:582-59-2 SDS

582-59-2Upstream product

582-59-2Downstream Products

582-59-2Relevant academic research and scientific papers

Free radical coupling of o -semiquinones uncovered

Pezzella, Alessandro,Crescenzi, Orlando,Panzella, Lucia,Napolitano, Alessandra,Land, Edward J.,Barone, Vincenzo,D'Ischia, Marco

supporting information, p. 12142 - 12149 (2013/09/02)

As a rule, o-semiquinones decay through disproportionation leading to equimolar amounts of catechol and o-quinone products. However, the o-semiquinone 1S generated by pulse radiolysis oxidation of the eumelanin precursor 5,6-dihydroxyindole (1) decays wit

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