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16948-63-3

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16948-63-3 Usage

Classification

Organic compound

Functional Groups

Amino group ($-NH2$)
Sulfonamide group ($-SO2NH2$)

Substituents

Two chlorine atoms (Cl) attached to the benzene ring

Application

Pharmaceutical Intermediate: Used in the synthesis of various drugs, particularly those with antibacterial and antimicrobial properties.
Agricultural Use: Component in pesticides and herbicides.
Scientific Research: Chemical reagent and in the development of new pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 16948-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,4 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16948-63:
(7*1)+(6*6)+(5*9)+(4*4)+(3*8)+(2*6)+(1*3)=143
143 % 10 = 3
So 16948-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H6Cl2N2O2S/c7-3-1-5(9)6(2-4(3)8)13(10,11)12/h1-2H,9H2,(H2,10,11,12)

16948-63-3SDS

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 2-amino-4,5-dichlorobenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-amino-4,5-dichloro-benzenesulfonamide

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:16948-63-3 SDS

16948-63-3Relevant articles and documents

Hydroxylated analogues of ATP-sensitive potassium channel openers belonging to the group of 6- and/or 7-substituted 3-Isopropylamino-4H-1,2,4- benzothiadiazine 1,1-dioxides: Toward an improvement in sulfonylurea receptor 1 selectivity and metabolism stabi

De Tullio, Pascal,Servais, Anne-Catherine,Fillet, Marianne,Gillotin, Florian,Somers, Fabian,Chiap, Patrice,Lebrun, Philippe,Pirotte, Bernard

, p. 8353 - 8361 (2011)

Diversely substituted 3-isopropylamino-4H-1,2,4-benzothiadiazine 1,1-dioxides are known to be potent KATP channel openers, with several drugs being selective for the SUR1/Kir6.2 channel subtype. This work examined the biological activity, tissu

Heteropolycyclic systems. I. 2,3-Dihydro-1H-pyrrol(2,1-c) (1,2,4) benzothiadiazine-5,5-dioxide and its derivatives

Cameroni,Ferioli,Bernabei

, p. 574 - 581 (2007/10/09)

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