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4-hydroxy-3-methyl-5-nitrobenzenesulphonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85895-88-1

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85895-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85895-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,9 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85895-88:
(7*8)+(6*5)+(5*8)+(4*9)+(3*5)+(2*8)+(1*8)=201
201 % 10 = 1
So 85895-88-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO6S/c1-4-2-5(15(12,13)14)3-6(7(4)9)8(10)11/h2-3,9H,1H3,(H,12,13,14)

85895-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-3-methyl-5-nitrobenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names EINECS 288-763-8

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:85895-88-1 SDS

85895-88-1Downstream Products

85895-88-1Relevant academic research and scientific papers

Structure-reactivity correlations in the dissociative hydrolysis of 2′,4′-dinitrophenyl 4-hydroxy-X-benzenesulfonates

Cevasco, Giorgio,Thea, Sergio

, p. 6814 - 6817 (2007/10/03)

The hydrolysis reactions of several title esters in water at 60°C follow the rate law kobs = (ka + kb[OH-])/(1 + αH/Ka), where Ka is the ionization constant of the hydroxy group of the ester and kb is the second-order rate constant for the SN2(S) attack of hydroxide ion on the ionized ester. Hammett and Br?nsted correlations are consistent with a previous proposal that the mechanism related to ka is dissociative. An unusual relationship between ka values and redox equilibrium constants for substituted quinones is found to hold: this finding further supports the dissociative nature of the pathway related to ka.

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