654072-71-6 Usage
Uses
Used in Pharmaceutical Industry:
2-ACETYLAMINO-THIAZOLE-5-SULFONYL CHLORIDE is used as a key building block for the synthesis of a variety of drugs and pharmaceuticals. Its unique structure allows for the development of new medicinal compounds with potential therapeutic applications.
Used in Organic Synthesis:
As a versatile reagent, 2-ACETYLAMINO-THIAZOLE-5-SULFONYL CHLORIDE is utilized in the synthesis of heterocyclic compounds, which are essential components in many organic and medicinal chemistry applications.
Used in Agrochemical Production:
2-ACETYLAMINO-THIAZOLE-5-SULFONYL CHLORIDE is used as an intermediate in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Dye Manufacturing:
2-ACETYLAMINO-THIAZOLE-5-SULFONYL CHLORIDE is also employed in the synthesis of dyes, where its reactive nature aids in the creation of a diverse range of colorants for various industries.
Used in Specialty Chemicals Production:
2-ACETYLAMINO-THIAZOLE-5-SULFONYL CHLORIDE's reactivity and structural properties make it suitable for use as an intermediate in the production of specialty chemicals, which have specific applications in industries such as plastics, coatings, and textiles.
Check Digit Verification of cas no
The CAS Registry Mumber 654072-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,4,0,7 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 654072-71:
(8*6)+(7*5)+(6*4)+(5*0)+(4*7)+(3*2)+(2*7)+(1*1)=156
156 % 10 = 6
So 654072-71-6 is a valid CAS Registry Number.
654072-71-6Relevant academic research and scientific papers
Aminarshad, Farzaneh,Heidari, Shima,Mostajeran, Neda,Massah, Ahmad Reza
, p. 547 - 562 (2022)
A simple cost-effective and green method was presented for the synthesis of coumarin bis sulfonamides. Seventeen novel coumarin sulfonamides were synthesized in good to high yield and purity in six steps starting from 2-amino thiazole, aniline, and 4-methoxy aniline. All of the reactions have been done under green conditions without using any hazardous solvent. The chemical structures of the products were elucidated by IR, 1H NMR, and 13C NMR spectroscopy and elemental analysis. Also, the anti-bacterial properties of the synthesized sulfonamides were investigated using two strains of Staphylococcus (gram-positive) and Escherichia coli (gram-negative) bacteria.
