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88801-93-8

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88801-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88801-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,0 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88801-93:
(7*8)+(6*8)+(5*8)+(4*0)+(3*1)+(2*9)+(1*3)=168
168 % 10 = 8
So 88801-93-8 is a valid CAS Registry Number.

88801-93-8SDS

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 benzenesulfonic acid,(3-bromophenyl)methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,3-bromo-,benzenesulfonate

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:88801-93-8 SDS

88801-93-8Downstream Products

88801-93-8Relevant articles and documents

Kinetics of the Reaction of Benzenesulfonyl Chloride with Substituted Benzoate Ions in Methanol

Banjoko, O.,Okwuiwe, R.

, p. 4966 - 4968 (2007/10/02)

The rate constants and activation parameters for the reaction of benzenesulfonyl chloride with substituted benzoate ions have been measured in methanol.The reaction is second order overall and first order with respect to each reactant.The rate constants are greater with electron-donating substituents while they are lower with electron-withdrawing groups.The substituent effects are correlated by Hammett (ρ -0.35) and Broensted (β 0.35) equations, respectively, and the results compared with the corresponding data for the reaction of benzenesulfonyl chloride with substituted anilines and related reactions.The kinetic results are interpreted in terms of a synchronous direct bimolecular nucleophilic displacement mechanism.

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