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20389-01-9

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20389-01-9 Usage

General Description

2,6-DIIODO-P-BENZOQUINONE, also known as 2,6-diiodo-1,4-benzoquinone, is a chemical compound with the molecular formula C6H2I2O2. It is a dark brown solid that is soluble in organic solvents. 2,6-DIIODO-P-BENZOQUINONE is commonly used in organic synthesis as a reagent for the synthesis of various other organic compounds. It is also used in the production of dyes, pharmaceuticals, and other industrial products. Additionally, 2,6-DIIODO-P-BENZOQUINONE has been studied for its potential use in anti-tumor and anti-microbial applications. However, it is important to handle this chemical with care, as it can be harmful if ingested or inhaled, and may cause skin and eye irritation upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 20389-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20389-01:
(7*2)+(6*0)+(5*3)+(4*8)+(3*9)+(2*0)+(1*1)=89
89 % 10 = 9
So 20389-01-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H2I2O2/c7-4-1-3(9)2-5(8)6(4)10/h1-2H

20389-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-diiodocyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2,6-Diiodoquinone

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:20389-01-9 SDS

20389-01-9Relevant articles and documents

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Kvalnes

, p. 670 (1934)

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Model reactions of thyroxine biosynthesis. Identification of the key intermediates in thyroxine formation from 3,5-diiodo-L-tyrosine and 4-hydroxy-3,5-diiodophenylpyruvic acid

Oza,Salamonczyk,Guo,Sih

, p. 11315 - 11316 (2007/10/03)

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