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N-(2,6-Dichloro-3-methylphenyl)-5,7-dichloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide is a sulfonamide derivative characterized by its potential antifungal and antibacterial properties. N-(2,6-Dichloro-3-methylphenyl)-5,7-dichloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide is distinguished by its unique chemical structure, which includes a triazolopyrimidine core and a dichloro-methylphenyl group, contributing to its ability to interfere with the metabolic processes of fungi and bacteria. Its promising characteristics position it as a candidate for the development of new pharmaceutical agents aimed at treating a variety of infections.

134892-32-3

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134892-32-3 Usage

Uses

Used in Pharmaceutical Development:
N-(2,6-Dichloro-3-methylphenyl)-5,7-dichloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide is utilized as a key component in the research and development of novel pharmaceutical agents. Its application is primarily for the treatment of infections caused by fungi and bacteria, where it may inhibit their growth by disrupting the synthesis of essential cellular components.
Used in Antifungal and Antibacterial Applications:
In the medical and pharmaceutical industry, N-(2,6-Dichloro-3-methylphenyl)-5,7-dichloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide serves as an antifungal and antibacterial agent. It is used for its ability to combat infections by interfering with the metabolic pathways necessary for the survival and replication of fungi and bacteria, thereby contributing to the control and eradication of such pathogens.
Used in Research and Discovery:
N-(2,6-Dichloro-3-methylphenyl)-5,7-dichloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide is also employed in scientific research to explore its potential mechanisms of action and to identify new targets for anti-infective therapies. Its unique structure and activity provide a foundation for further investigation into its therapeutic potential and possible applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 134892-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,9 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 134892-32:
(8*1)+(7*3)+(6*4)+(5*8)+(4*9)+(3*2)+(2*3)+(1*2)=143
143 % 10 = 3
So 134892-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H7Cl4N5O2S/c1-5-2-3-6(13)10(9(5)16)20-24(22,23)12-18-11-17-7(14)4-8(15)21(11)19-12/h2-4,20H,1H3

134892-32-3SDS

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 5,7-dichloro-N-(2,6-dichloro-3-methylphenyl)-[1,2,4]triazolo[1,5-a]pyrimidine-2-sulfonamide

1.2 Other means of identification

Product number -
Other names N-(2,6-dichloro-3-methylphenyl)-5,7-dichloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide

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:134892-32-3 SDS

134892-32-3Downstream Products

134892-32-3Relevant academic research and scientific papers

Preparation of 5,7-dihydroxy-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonanilides

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, (2008/06/13)

5,7-Dihydroxy-N-(aryl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides are prepared by the cyclization of N-(3-(((aryl)amino)sulfonyl)-1H-1,2,4-triazol-5-yl)amines with malonyl halides under acidic conditions. With the addition of a phosphorus oxyhalide, m

Substituted 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides, compositions containing them, and their utility as herbicides

-

, (2008/06/13)

Novel substituted triazolo[1,5-a]pyrimidine-2-sulfonamides, e.g., 5,7-dimethyl-N-(2,6-dichlorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide and their agriculturally acceptable salts are prepared. These compounds and compositions containing them are useful for the control of unwanted vegetation. Novel substituted triazolo[1,5-a]pyrimidine-2-sulfonyl chlorides and substituted anilines and their use as intermediates are also described.

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