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3,4-disulfanylcyclobut-3-ene-1,2-dithione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56284-07-2

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56284-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56284-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,8 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56284-07:
(7*5)+(6*6)+(5*2)+(4*8)+(3*4)+(2*0)+(1*7)=132
132 % 10 = 2
So 56284-07-2 is a valid CAS Registry Number.

56284-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name potassium,3,4-bis(sulfanyl)cyclobut-3-ene-1,2-dithione

1.2 Other means of identification

Product number -
Other names Kalium-tetrathioquadratat

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:56284-07-2 SDS

56284-07-2Downstream Products

56284-07-2Relevant academic research and scientific papers

Electrochemistry of squarate and thiosquarate dianions

Carre, B.,Paris, J.,Fabre, P. L.,Jourdannaud, S.,Castan, P.,et al.

, p. 367 - 374 (2007/10/02)

Squarate dianion C4O42- and its thiosquarate C4O(4-x)Sx2- (x=1, 2, 4) derivatives have been shown to be ligating agents towards metal ions.Their electrochemical properties in aprotic solvent (acetonitrile) is revisited, with the goal of generating radical-anions by anodic oxidation of the dianions.Among these compounds, only C4O42- leads by anodic oxidation to a radical-anion C4O4.-, stabilized by electron delocalization.The thioderivatives form disulfides by radical condensation which suggests that the electron is localized on the sulfur atoms.

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