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1,4-Benzenedimethanol, 2,3-dihydroxyis a chemical compound with the molecular formula C8H10O4. It is a derivative of benzene and contains two hydroxyl groups attached to the benzene ring. This versatile compound can undergo various chemical reactions, such as esterification and oxidation, to produce a wide range of products.

80067-65-8

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80067-65-8 Usage

Uses

Used in Plastics Industry:
1,4-Benzenedimethanol, 2,3-dihydroxyis used as a building block for the synthesis of various polymers, contributing to the development of new materials with improved properties.
Used in Adhesives Industry:
1,4-Benzenedimethanol, 2,3-dihydroxyis used as a component in the formulation of adhesives, enhancing their bonding strength and durability.
Used in Coatings Industry:
1,4-Benzenedimethanol, 2,3-dihydroxyis used in the production of coatings, providing improved performance and resistance to various environmental factors.
Used in Pharmaceutical Industry:
1,4-Benzenedimethanol, 2,3-dihydroxyis used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapies.
It is important to handle 1,4-Benzenedimethanol, 2,3-dihydroxywith care due to its potential health hazards and environmental impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 80067-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80067-65:
(7*8)+(6*0)+(5*0)+(4*6)+(3*7)+(2*6)+(1*5)=118
118 % 10 = 8
So 80067-65-8 is a valid CAS Registry Number.

80067-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-bis(hydroxymethyl)benzene-1,2-diol

1.2 Other means of identification

Product number -
Other names 3,6-Bis-hydroxymethyl-brenzcatechin

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:80067-65-8 SDS

80067-65-8Relevant academic research and scientific papers

Electroorganic reactions. Part 55. Quinodimethane chemistry. Part 3. Transition metal complexes as inter- and intra-molecular redox catalysts for the electrosynthesis of poly(p-xylylene) (PPX) polymers and oligomers

Janssen,Utley,Carre?,Simon,Schirmer

, p. 1573 - 1584 (2007/10/03)

The role of metal complexes as redox mediators in the electrosynthesis of poly(p-xylylenes) (PPXs) has been explored, with a view to designing metal-containing precursors that can act both as mediators and starting materials for metal-containing polymers. A number of transition metal complexes [Cr(III), Ni(II) and Co(II)] are efficient redox catalysts for production of quinodimethanes, and hence PPXs. Following encouraging results from experiments using mediators based on anthranilic acid and salicylaldehyde ligands a macrocyclic compound was designed, and successfully prepared by a convergent route that incorporated both a 1,4-bis(chloromethylarene) function as a precursor to a quinodimethane and a Ni(II) salen unit as an intramolecular redox catalyst. The macrocycle was successfully reduced cathodically to yield a PPX polymer with bound Ni(II). Evidence is presented for the operation of intramolecular redox catalysis (homomediation).

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