4113-57-9 Usage
Uses
Used in Pharmaceutical Industry:
5-Chloro-1,2,3-thiadiazole serves as a valuable building block for the synthesis of a wide range of pharmaceuticals and agrochemicals. Its unique structure allows for the development of new drugs with potential therapeutic effects.
Used in Organic Synthesis:
As a reagent, 5-Chloro-1,2,3-thiadiazole is utilized in organic synthesis processes, contributing to the creation of various organic compounds with specific properties and applications.
Used in Dye and Pigment Production:
5-Chloro-1,2,3-thiadiazole also acts as an intermediate in the production of dyes and pigments, enabling the development of colorants for different applications, such as textiles, plastics, and printing inks.
Safety Precautions:
Due to its moderate toxicity, 5-Chloro-1,2,3-thiadiazole should be handled and used with appropriate safety measures. This includes wearing protective equipment, working in well-ventilated areas, and following proper disposal procedures to minimize potential health and environmental risks.
Check Digit Verification of cas no
The CAS Registry Mumber 4113-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4113-57:
(6*4)+(5*1)+(4*1)+(3*3)+(2*5)+(1*7)=59
59 % 10 = 9
So 4113-57-9 is a valid CAS Registry Number.
InChI:InChI=1/C2HClN2S/c3-2-1-4-5-6-2/h1H
4113-57-9Relevant academic research and scientific papers
Substituted 1-propiolylpiperazine compounds, their preparation and use
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, (2008/06/13)
Substituted 1-propiolylpiperazine compounds corresponding to formula I in which X denotes N or C—R2, and n is an integer from 0 to 8, a method for producing such substituted 1-propiolylpiperazine compounds, pharmaceutical compositions containing such substituted 1-propiolylpiperazine compounds, and the use of such substituted 1-propiolylpiperazine compounds for modulating mGluR5 receptor activity or for treating or inhibiting pain and various other conditions, especially conditions at least partly mediated by the mGluR5 receptor.
Process for making 5-amino-1,2,3-thiadiazoles
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, (2008/06/13)
5-amino-1,2,3-thiadiazoles of the formula STR1 are made by reacting halogenoacetaldehydes of the formula with hydrazine derivatives of the formula preferably in an aqueous medium or in a mixture of an aqueous medium with organic solvents so as to form acylhydrazones of the formula whereupon the latter are reacted with thionylchloride of the formula whereby 5-halogeno-1,2,3-thiadiazoles are formed which are then reacted with ammonia preferably in the presence of a catalyst such as a mineral acid or Lewis acid whereby the desired product is obtained. The products are useful in making plant protection agents and herbicides such as the 1,2,3-thiadiazolyl-urea derivatives.
