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17260-67-2

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17260-67-2 Usage

Description

2-Chloro-N-methylbenzenesulphonamide, a sulphonamide derivative with the molecular formula C7H8ClNO2S, is a white to off-white water-soluble chemical compound. It is widely recognized for its antimicrobial properties and is utilized in various industrial and medical applications.

Uses

Used in Pharmaceutical Industry:
2-Chloro-N-methylbenzenesulphonamide is used as an antimicrobial agent for its ability to inhibit the growth of bacteria, making it a valuable component in the development of pharmaceuticals aimed at treating bacterial infections.
Used in Manufacturing of Dyes:
In the dye industry, 2-Chloro-N-methylbenzenesulphonamide is utilized in the production of dyes, contributing to the coloration and stability of various products.
Used as a Preservative:
2-Chloro-N-methylbenzenesulphonamide is used as a preservative in different products to prevent microbial contamination and extend the shelf life of the products.
Used in Chemical Synthesis:
2-Chloro-N-methylbenzenesulphonamide serves as a solubilizing agent in the synthesis of other chemicals, facilitating the process and improving the efficiency of chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 17260-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17260-67:
(7*1)+(6*7)+(5*2)+(4*6)+(3*0)+(2*6)+(1*7)=102
102 % 10 = 2
So 17260-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8ClNO2S/c1-9-12(10,11)7-5-3-2-4-6(7)8/h2-5,9H,1H3

17260-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-N-methylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-Methyl-2-chlor-benzol-sulfonamid

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:17260-67-2 SDS

17260-67-2Downstream Products

17260-67-2Relevant articles and documents

Recyclable covalent triazine framework-supported iridium catalyst for the N-methylation of amines with methanol in the presence of carbonate

Liu, Peng,Yang, Jiazhi,Ai, Yao,Hao, Shushu,Chen, Xiaozhong,Li, Feng

, p. 281 - 290 (2021/03/26)

An iridium complex Cp*Ir@CTF, which is synthesized by the coordinative immobilization of [Cp*IrCl2]2 on a functionalized covalent triazine framework (CTF), was found to be a general and highly efficient catalyst for the N-methylation of amines with methanol in the presence of carbonate. Under environmentally benign conditions, a variety of desirable products were obtained in high yields with complete selectivities and functional group friendliness. Furthermore, the synthesized catalyst could be recycled by simple filtration without obvious loss of catalytic activity after sixth cycle. Notably, this research exhibited the potential of covalent triazine framework-supported transition metal catalysts for hydrogen autotransfer process.

N-Methylation of Amines with Methanol in Aqueous Solution Catalyzed by a Water-Soluble Metal-Ligand Bifunctional Dinuclear Iridium Catalyst

Han, Xingyou,Li, Feng,Liu, Peng,Meng, Chong,Tung, Nguyen Thanh

, p. 5815 - 5824 (2020/05/26)

The N-methylation of amines with methanol in aqueous solution was proposed and accomplished by using a water-soluble metal-ligand bifunctional dinuclear iridium catalyst. In the presence of [(Cp*IrCl)2(thbpym)][Cl]2 (1 mol %), a range of desirable products were obtained in high yields under environmentally benign conditions. Notably, this research exhibited the potential of transition metal-catalyzed activation of methanol as a C1 source for the construction of the C-N bond in aqueous solution.

TACHYKININ RECEPTOR ANTAGONISTS

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Page 61, (2010/02/10)

The present invention relates to selective NK-1 receptor antagonists of Formula (I) or a pharmaceutically acceptable salt thereof, for the treatment of disorders associated with an excess of tachykinins.

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