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cyclohexa-2,5-diene-1,4-dione - 2-methylbenzene-1,4-diol (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55836-33-4

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55836-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55836-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,3 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55836-33:
(7*5)+(6*5)+(5*8)+(4*3)+(3*6)+(2*3)+(1*3)=144
144 % 10 = 4
So 55836-33-4 is a valid CAS Registry Number.

55836-33-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexa-2,5-diene-1,4-dione,2-methylbenzene-1,4-diol

1.2 Other means of identification

Product number -
Other names cyclohexa-2,5-diene-1,4-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:55836-33-4 SDS

55836-33-4Relevant academic research and scientific papers

SOLID-STATE FORMATION OF QUINHYDRONES FROM THEIR COMPONENTS. USE OF SOLID-SOLID REACTIONS TO PREPARE COMPOUNDS NOT ACCESSIBLE FROM SOLUTION.

Patil,Curtin,I. C. Paul

, p. 348 - 353 (2007/10/02)

Selective molecular mobility provided by working with crystalline solids has been employed to prepare unsymmetrically substituted quinhydrones too unstable with respect to self-oxidation-reduction to be prepared by crystallization from solution. Reaction is carried out by grinding the solid components together with a mortar and pestle. Examination of the products with differential scanning calorimetry, X-ray powder photography, and Fourier transform infrared spectroscopy shows that the complexation reaction goes to completion under conditions in which no detectible redox reaction has occurred. The products are shown by X-ray powder photography to be formed in a microcrystalline state.

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