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Benzenesulfonic acid, 2-chloro-4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78846-76-1

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78846-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78846-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,4 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78846-76:
(7*7)+(6*8)+(5*8)+(4*4)+(3*6)+(2*7)+(1*6)=191
191 % 10 = 1
So 78846-76-1 is a valid CAS Registry Number.

78846-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-nitrobenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names Benzenesulfonic acid,2-chloro-4-nitro

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:78846-76-1 SDS

78846-76-1Downstream Products

78846-76-1Relevant academic research and scientific papers

Method for synthesizing p-nitrobenzenesulfonic

-

Paragraph 0008, (2016/10/07)

The invention relates to a method for synthesizing p-nitrobenzenesulfonic and belongs to the technical field of organic chemical synthesis. The method comprises the steps of subjecting benzene serving as the raw material and sulfuric acid to sulfonation to obtain benzenesulfonic acid; pumping chlorine into benzenesulfonic acid, adding deionized water and zinc dibutyl dithiocaarbamate, and stirring the mixture; adding nitric acid and acetic anhydride into the mixture for water-bath heating, and then performing cooling through ice water; slowly adding a sodium hydroxide solution dropwise into the cooled mixture, performing heating reflux after dropping reaction, cooling the mixture to the room temperature, and obtaining p-nitrobenzenesulfonic through separation, recovery and drying. The method has the advantages that the reaction time is shortened by 30% of time needed by a 3-nitrobenzene acid synthesis method, pollution cannot be produced during reaction, and operation steps are simple.

Micro determination of furosemide pure and some of its pharmaceutical preparations with ammonium hexanitratocerate (IV) reagent

Suraiya, Afshan,Singh, Siddharth,Chauhan

experimental part, p. 1799 - 1802 (2012/06/15)

A new method has been developed for the micro determination of furosemide pure and some of its pharmaceutical preparations by using Ce(IV) reagent as oxidant. The method is simple, accurate, sensitive and gives reproducible results within ± 1% error. Effects of different variables have been studied and SD & CV calculated. Recovery experiment is carried out by standard drug addition method. A probable reaction mechanism has also been suggested. Interference of various ions has been studied.

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