75272-54-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 3 carbon atoms, 3 hydrogen atoms, 3 nitrogen atoms, 1 oxygen atom, and 1 sulfur atom.
2. Derivative of Thiadiazole Ring System
Explanation
The compound is derived from the thiadiazole ring system, which is a five-membered ring containing two nitrogen atoms and one sulfur atom.
3. Contains Carboxamide and N-Hydroxy Functional Groups
Explanation
The compound has two functional groups a carboxamide group (-CONH2) and an N-hydroxy group (-NOH). These groups contribute to the compound's chemical properties and potential applications.
4. Potential Pharmaceutical Applications
Explanation
The compound has been studied for its potential use in the development of drugs with various therapeutic properties, such as anticancer, anti-inflammatory, and antimicrobial.
5. Anticancer Properties
Explanation
The compound may have the ability to inhibit the growth of cancer cells or interfere with their survival mechanisms, making it a potential candidate for cancer treatment.
6. Anti-Inflammatory Properties
Explanation
The compound may help reduce inflammation by modulating the immune response or targeting specific inflammatory pathways.
7. Antimicrobial Properties
Explanation
The compound may exhibit activity against microorganisms, such as bacteria, fungi, or viruses, making it a potential candidate for the development of new antimicrobial drugs.
8. N-Hydroxy Group as a Key Feature
9. Potential as a Metal Chelator
Explanation
The compound may have the ability to bind and sequester metal ions, which could be useful in various applications, such as treating metal poisoning or developing new materials with specific properties.
10. Potential as a Corrosion Inhibitor
Explanation
The compound may have the ability to slow down or prevent the corrosion of metals, which could be useful in various industrial applications, such as protecting infrastructure or improving the longevity of materials.
11. Further Research Needed
Explanation
More research is required to fully understand the potential applications and characteristics of 1,2,3-Thiadiazole-5-carboxamide, N-hydroxy-(9CI), as well as to optimize its properties and develop new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 75272-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75272-54:
(7*7)+(6*5)+(5*2)+(4*7)+(3*2)+(2*5)+(1*4)=137
137 % 10 = 7
So 75272-54-7 is a valid CAS Registry Number.
75272-54-7Relevant academic research and scientific papers
Process for making 5-mercapto-1,2,3-triazoles
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, (2008/06/13)
A process for making 5-mercapto-1,2,3-triazoles of the formula STR1 wherein R1 is hydrogen or a C1 -C4 -alkyl which may also be substituted, the said process comprising (1) as a first step reacting a solution of 1,2,3-thiadiazole-5-carbohydroxamic acid derivative of the formula STR2 wherein R1 has the meaning as above and R2 is hydrogen or a univalent metal equivalent in an inert organic solvent in the presence of an acid acceptor with a solution in an inert organic solvent of an acid halide of the formula so as to form an acylated 1,2,3-thiadiazole-5-carbohydroxamic acid derivative (2) reacting as a solution in an inert organic solvent the carbohydroxamic acid derivative just obtained with an alcohol or phenol of the formula so as to form a (1,2,3-thiadiazole-5-yl)-carbamic acid ester (3) then treating the thus obtained carbamic acid ester with an acetic or basic catalyst to form the 5-amino-1,2,3-thiadiazole (4) whereupon the said amino thiadiazole is subject to a rearrangement in the presence of a base followed by isolation of the product of the reaction.
