175205-72-8 Usage
Uses
Used in Pharmaceutical Synthesis:
3-BROMO-5-CHLOROTHIOPHENE-2-SULFONYL CHLORIDE is used as an intermediate for the synthesis of pharmaceutical products. Its strong electrophilic nature makes it a valuable tool in various chemical reactions and transformations, facilitating the creation of biologically active compounds with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 3-BROMO-5-CHLOROTHIOPHENE-2-SULFONYL CHLORIDE is utilized as a key intermediate in the production of agrochemical products. Its role in the synthesis of active ingredients for pesticides and other agrochemicals contributes to the development of effective solutions for crop protection and management.
Used in Fine Chemicals Manufacturing:
3-BROMO-5-CHLOROTHIOPHENE-2-SULFONYL CHLORIDE is employed as a building block in the production of fine chemicals. Its versatility in organic synthesis allows for the creation of a wide range of specialty chemicals used in various industries, including fragrances, dyes, and other high-value applications.
Overall, 3-BROMO-5-CHLOROTHIOPHENE-2-SULFONYL CHLORIDE's unique chemical properties and strong electrophilicity make it an essential component in the synthesis of various compounds across different sectors, highlighting its significance in modern chemical research and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 175205-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,0 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 175205-72:
(8*1)+(7*7)+(6*5)+(5*2)+(4*0)+(3*5)+(2*7)+(1*2)=128
128 % 10 = 8
So 175205-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrClO2S/c1-5-2-6(8)4-7(3-5)12(9,10)11/h2-4H,1H3
175205-72-8Relevant academic research and scientific papers
Novel process
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, (2008/06/13)
The present invention relates to a novel processes for preparing pharmaceutically active fused 1,2,4-thiadiazine derivatives of general formula (I) as defined in the description and intermediates therefore.
