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1,2,5,8-dithiadiazecane-4,9-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25286-76-4

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25286-76-4 Usage

Type of compound

Heterocyclic compound

Structure

Six-membered ring containing two nitrogen and two sulfur atoms

Known for

Ability to form stable radicals

Potential applications

Organic electronics and materials science

Synthesized and studied for

Optical and electronic properties

Potential use

Organic semiconductors and photovoltaic devices

Field of interest

Organic and materials chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 25286-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,8 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25286-76:
(7*2)+(6*5)+(5*2)+(4*8)+(3*6)+(2*7)+(1*6)=124
124 % 10 = 4
So 25286-76-4 is a valid CAS Registry Number.

25286-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5,8-dithiadiazecane-4,9-dione

1.2 Other means of identification

Product number -
Other names perhydro 1,2-dithia-5,8-diazecine-4,9-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:25286-76-4 SDS

25286-76-4Downstream Products

25286-76-4Relevant academic research and scientific papers

Synthesis of cyclic functionalized bisulfides and their oligomers

Bonnans-Plaisance,Levesque,Toulin

, p. 231 - 244 (1998)

In order to obtain comonomers for the free-radical polymerization of acrylic or vinylic monomers, cyclic disufides were synthesized. Ester or amide functions were introduced in these cyclic molecules in order to afford easily degradable centers in the cop

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