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2,4-DIMETHOXY-THIOBENZAMIDE, a chemical compound with the molecular formula C9H9NO3S, is a derivative of thioacetanilide, which belongs to a class of organic compounds that contain a thioamide group. It is recognized for its versatile chemical properties, making it a valuable intermediate in various industrial applications.

23822-07-3

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23822-07-3 Usage

Uses

Used in Pharmaceutical Industry:
2,4-DIMETHOXY-THIOBENZAMIDE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique chemical structure allows it to be a building block in the creation of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-DIMETHOXY-THIOBENZAMIDE is utilized as an intermediate in the production of agrochemicals, playing a role in the development of pesticides and other agricultural chemicals that are essential for crop protection and yield enhancement.
Used in Dye and Pigment Production:
2,4-DIMETHOXY-THIOBENZAMIDE is used as a chemical intermediate in the manufacturing of dyes and pigments, contributing to the coloration and stability of these products in various applications, including textiles, plastics, and printing inks.
Used in Materials Science:
2,4-DIMETHOXY-THIOBENZAMIDE also finds application in the field of materials science, where it is used to develop new materials with specific properties, such as improved conductivity, stability, or reactivity, depending on the desired application.

Check Digit Verification of cas no

The CAS Registry Mumber 23822-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,2 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23822-07:
(7*2)+(6*3)+(5*8)+(4*2)+(3*2)+(2*0)+(1*7)=93
93 % 10 = 3
So 23822-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2S/c1-11-6-3-4-7(9(10)13)8(5-6)12-2/h3-5H,1-2H3,(H2,10,13)

23822-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethoxybenzenecarbothioamide

1.2 Other means of identification

Product number -
Other names 2,4-dimethoxy-thiobenzamide

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:23822-07-3 SDS

23822-07-3Relevant academic research and scientific papers

Novel thiazole derivatives as inhibitors of superoxide production by human neutrophils: Synthesis and structure-activity relationships

Chihiro,Nagamoto,Takemura,Kitano,Komatsu,Sekiguchi,Tabusa,Mori,Tominaga,Yabuuchi

, p. 353 - 358 (2007/10/02)

Neutrophils have an important role in the self-defense systems of organisms through the production of superoxide. On the other hand, it has been proposed that abnormal amounts of superoxide produced by neutrophils are a serious factor in tissue injury. A series of novel thiazole derivatives was prepared and evaluated inhibitory effect on superoxide production by human neutrophils in vitro. Among these compounds, 6-[2-(3,4- diethoxyphenyl)thiazol-4-yl]-pyridine-2-carboxylic acid (OPC-6535) was selected as one of the most promising compounds. The synthesis and structure- activity relationships of these compounds are reported herein.

Process for the preparation of aromatic thiocarboxylic acid amides

-

, (2008/06/13)

Aromatic thiocarboxylic acid amides are prepared by reaction of aromatic hydrocarbons with hydrogen thiocyanate or a salt of thiocyanic acid in at least 90% hydrofluoric acid. The reaction can be carried out in one single operation without the use of a Lewis acid or another catalyst. The thiocarboxylic acid amides obtained are known from the literature and serve as preliminary products for the preparation of nitriles, amides, carboxylic acids, heterocyclic compounds and the manufacture of plant protecting agents and pharmaceuticals.

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