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Phosphonic acid, mono(2-hydroxyphenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60798-82-5

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60798-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60798-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,9 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60798-82:
(7*6)+(6*0)+(5*7)+(4*9)+(3*8)+(2*8)+(1*2)=155
155 % 10 = 5
So 60798-82-5 is a valid CAS Registry Number.

60798-82-5SDS

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 2-[hydroxy(oxo)phosphaniumyl]oxyphenolate

1.2 Other means of identification

Product number -
Other names Phosphonic acid,mono(2-hydroxyphenyl) ester

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:60798-82-5 SDS

60798-82-5Downstream Products

60798-82-5Relevant academic research and scientific papers

Organophosphorus Antioxidants. II. Kinetics and Mechanism of the Decomposition of Alkylhydroperoxides by Esteramides of Phosphorous and Phosphoric Acid

Rueger, C.,Arnold, D.,Schwetlick, K.

, p. 706 - 716 (2007/10/02)

The reaction mechanism of 2-amido-1,3,2-benzodioxaphospholes (1) with cumyl and t-butylhydroperoxide has been studied kinetically by means of 31P-n.m.r. and e.p.r. spectroscopy and high pressure liquid chromatography. 1 reacts with cumyl hydroperoxide to give the corresponding 2-oxides (2) which with more hydroperoxide and/or water form the phosphate esters 7 and 8.These acidic phosphates decompose cumyl hydroperoxide catalytically giving phenol and aceton.All amides (1) react with t-butyl hydroperoxide stoichiometrically to give t-butanol.The ionic mechanism of hydroperoxide decomposition is accompanied in a minor proportion by a homolytical one.

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