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22185-11-1

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22185-11-1 Usage

General Description

2-(dimethylsulfamoyl)benzoic acid, also known as benzosulfonamide, is a chemical compound with the molecular formula C10H13NO4S. It is a derivative of benzoic acid and is commonly used as a sulfonamide antibiotic in the treatment of bacterial infections. The presence of a sulfonamide group in its structure gives benzosulfonamide its antimicrobial properties. It works by inhibiting the growth and reproduction of bacteria, making it an effective treatment for a variety of bacterial infections. Additionally, benzosulfonamide is also used as a preservative in cosmetics and personal care products due to its antimicrobial effects. Overall, 2-(dimethylsulfamoyl)benzoic acid is a valuable chemical with important applications in the medical and cosmetic industries.

Check Digit Verification of cas no

The CAS Registry Mumber 22185-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,8 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22185-11:
(7*2)+(6*2)+(5*1)+(4*8)+(3*5)+(2*1)+(1*1)=81
81 % 10 = 1
So 22185-11-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO4S/c1-10(2)15(13,14)8-6-4-3-5-7(8)9(11)12/h3-6H,1-2H3,(H,11,12)

22185-11-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylsulfamoyl)benzoic acid

1.2 Other means of identification

Product number -
Other names o-(N,N-Dimethyl-sulfamoyl)-benzoesaeure

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:22185-11-1 SDS

22185-11-1Relevant articles and documents

MODIFIED PROTEINS AND PROTEIN DEGRADERS

-

, (2021/12/08)

Provided herein are compounds, pharmaceutical compositions, and methods for binding or degrading target proteins. Further provided herein are compounds having a DNA damage-binding protein 1 (DDB1) binding moiety. Some such embodiments include a linker. Some such embodiments include a target protein binding moiety. Further provided herein are ligand-DDB1 complexes. Further provided herein are in vivo modified DDB1 proteins.

STRUCTURE AND REACTIVITY IN INTRAMOLECULAR CATALYSIS. CATALYSIS OF SULFONAMIDE HYDROLYSIS BY THE NEIGHBORING CARBOXY GROUP.

Graafland,Wagenaar,Kirby,Engberts

, p. 6981 - 6991 (2007/10/10)

A report is presented on kinetic data for the intramolecular carboxy-catalyzed hydrolysis of 26 sulfonamides in water and in some mixed aqueous solvents. The effective molarity of the carboxyl group is very high (up to ca. 10**8 M) but depends markedly on the structure of the sulfonamide. Substituent effects within a series of 4- and 5-substituted 2-carboxy-N,N-dimethylbenzenesulfonamides are interpreted in terms of nucleophilic catalysis. The role of nonbonded interactions in the initial state and in the transition state is discussed. By using X-ray structural data where available, strain effects have been elucidated for a series of sulfonamides in which the sulfonamide and carboxyl groups are held cis to each other. Striking differences from the corresponding carboxamide systems are attributed to differences in transition state geometries and steric effects.

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