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175276-92-3

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175276-92-3 Usage

Description

2,4-Difluorobenzene-1-carbothioamide is a chemical compound characterized by the molecular formula C7H4F2S. It is a thioamide derivative of benzene, featuring two fluorine atoms at the 2nd and 4th positions. 2,4-Difluorobenzene-1-carbothioamide is recognized for its utility in organic synthesis and as a key building block in the creation of innovative pharmaceuticals and agrochemicals. Additionally, it has garnered interest due to its potential antifungal and antibacterial properties, making it a significant chemical for research and development in both the chemical and medical fields.

Uses

Used in Organic Synthesis:
2,4-Difluorobenzene-1-carbothioamide is utilized as a synthetic intermediate for the preparation of various organic compounds. Its unique structure, with fluorine atoms and a thioamide group, allows for the creation of a wide range of chemical entities, contributing to the diversity of organic chemistry.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,4-Difluorobenzene-1-carbothioamide serves as a crucial building block for the development of new drugs. Its structural features make it a versatile component in the design and synthesis of molecules with potential therapeutic applications.
Used in Agrochemical Formulation:
2,4-Difluorobenzene-1-carbothioamide is also employed in the agrochemical sector, where it is used as a component in the formulation of new pesticides or other crop protection agents. Its chemical properties can be leveraged to enhance the effectiveness of these products.
Used in Antimicrobial Research:
2,4-Difluorobenzene-1-carbothioamide is used as a subject of study in antimicrobial research for its potential antifungal and antibacterial properties. This research aims to explore and understand its activity against various microorganisms, which could lead to the development of new treatments for microbial infections.
Used in Research and Development:
In the broader field of research and development, 2,4-Difluorobenzene-1-carbothioamide is a valuable chemical for exploring new reactions, mechanisms, and applications. Its unique structure and properties make it an interesting subject for scientific inquiry, potentially leading to breakthroughs in both chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 175276-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,7 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 175276-92:
(8*1)+(7*7)+(6*5)+(5*2)+(4*7)+(3*6)+(2*9)+(1*2)=163
163 % 10 = 3
So 175276-92-3 is a valid CAS Registry Number.

175276-92-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H26758)  2,4-Difluorothiobenzamide, 97%   

  • 175276-92-3

  • 1g

  • 1023.0CNY

  • Detail
  • Alfa Aesar

  • (H26758)  2,4-Difluorothiobenzamide, 97%   

  • 175276-92-3

  • 5g

  • 3149.0CNY

  • Detail

175276-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-difluorobenzenecarbothioamide

1.2 Other means of identification

Product number -
Other names 2,4-Difluoro-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:175276-92-3 SDS

175276-92-3Relevant articles and documents

FUSED HETEROCYCLIC COMPOUNDS AND THEIR USE

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Page/Page column 34; 35, (2014/03/25)

The present invention provides compounds of formula (I) and pharmaceutically acceptable salts, hydrates and solvates thereof for use in the treatment of cancer:

Reactions of some ortho and para halogenated aromatic nitriles with ethylenediamine: Selective synthesis of imidazolines

Crane, Louis J.,Anastassiadou, Maria,Stigliani, Jean-Luc,Baziard-Mouysset, Geneviève,Payard, Marc

, p. 5325 - 5330 (2007/10/03)

The reaction of ethylenediamine (EDA) with ortho and/or para halogenated benzonitriles did not lead to the imidazolines expected: a competitive aromatic nucleophilic substitution (SNAr) was observed instead. The selective synthesis of these imidazolines was performed by nucleophilic addition of EDA to thiobenzamide derivatives. The difference in reactivity between the nitrile and thioamide derivatives was estimated by a frontier orbital approach at the RHF/6-31G** level which predicted a greater reactivity of substituted thiobenzamides towards the nucleophilic addition of EDA.

Substituted 1,3-thiazole compounds, their production and use

-

, (2008/06/13)

(1) A 1,3-thiazole compound of which the 5-position is substituted with a 4-pyridyl group having a substituent including no aromatic group or (2) a 1,3-thiazole compound of which the 5-position is substituted with a pyridyl group having at the position adjacent to a nitrogen atom of the pyridyl group a substituent including no aromatic group has an excellent p38 MAP kinase inhibitory activity.

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