4100-20-3 Usage
Uses
Used in Pharmaceutical Industry:
1,2,3-Thiadiazole-4-carboxamide is used as an intermediate in the synthesis of various pharmaceuticals for its diverse biological activities, including antifungal, antibacterial, and other therapeutic properties. Its unique structure and functional groups enable the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
1,2,3-Thiadiazole-4-carboxamide is used as an intermediate in the synthesis of agrochemicals, such as herbicides, fungicides, and insecticides, due to its herbicidal and antifungal properties. Its incorporation into these products helps improve crop protection and yield by effectively controlling pests and diseases.
Used in Chemical Industry:
1,2,3-Thiadiazole-4-carboxamide is used in the production of dyes, pigments, and corrosion inhibitors. Its chemical properties and reactivity make it suitable for creating a variety of colorants and protective coatings, enhancing the performance and durability of various materials and products.
Used in Research and Development:
1,2,3-Thiadiazole-4-carboxamide serves as a valuable compound in research and development efforts, particularly in the fields of medicinal chemistry and materials science. Its unique structure and properties allow scientists to explore new applications and develop innovative products with improved performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 4100-20-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4100-20:
(6*4)+(5*1)+(4*0)+(3*0)+(2*2)+(1*0)=33
33 % 10 = 3
So 4100-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H3N3OS/c4-3(7)2-1-8-6-5-2/h1H,(H2,4,7)
4100-20-3Relevant academic research and scientific papers
Synthesis and antifungal activities of alkyl N-(1,2,3-thiadiazole-4-carbonyl) carbamates and S-alkyl N-(1,2,3-thiadiazole-4-carbonyl) carbamothioates
Li, Zaifeng,Wu, Zengru,Luo, Fuying
, p. 3872 - 3876 (2007/10/03)
A series of alkyl N-(1,2,3-thiadiazole-4-carbonyl) carbamates and S-alkyl N-(1,2,3-thiadiazole-4-carbonyl) carbamothioates with unsubstituted or monobrominated straight chain alkyl groups were synthesized and evaluated as fungistatic agents against Gibberella zeae and Altemaria kikuchiana. These compounds showed variable antifungal activities at concentrations of 5 and 50 μg/mL The results showed that antifungal activities depended on the length of the alkyl chain with the optimal chain length of 6-11 carbons. Carbamic acid, (1,2,3-thiadiazole-4-ylcarbonyl)-, hexyl ester (4) showed a strong fungistatic activity against A. kikuchiana at both concentrations, with 90.7 and 54% growth inhibition at 50 and 5 μg/mL, respectively. Carbamic acid, (1,2,3-thiadiazole-4-ylcarbonyl)-, heptyl ester (5); Carbamic acid, (1,2,3-thiadiazole-4-ylcarbonyl)-, octyl ester (6); and Carbamic acid, (1,2,3-thiadiazole-4-ylcarbonyl)-, undecyl ester (9) showed strong fungistatic activity against G. zeae at both concentrations. Their growth inhibitions against G. zeae at the concentration of 5 μg/mL were 78, 63, and 59%, respectively.
