119458-67-2 Usage
Uses
Used in Pharmaceutical Industry:
[4-(2-Hydroxy-phenyl)-[1,2,5]thiadiazol-3-yl]-morpholin-4-yl-methanone is used as a potential drug candidate for its anti-inflammatory, anti-tumor, and anti-microbial properties. [4-(2-Hydroxy-phenyl)-[1,2,5]thiadiazol-3-yl]-morpholin-4-yl-methanone's ability to exhibit these activities makes it a valuable asset in the development of new medications to treat various diseases and conditions.
Used in Drug Solubility Enhancement:
In the pharmaceutical industry, [4-(2-Hydroxy-phenyl)-[1,2,5]thiadiazol-3-yl]-morpholin-4-yl-methanone is used as a solubility enhancer for other drug compounds. The presence of the morpholine group improves the solubility of drugs, which can lead to better pharmacokinetic properties and increased bioavailability.
Used in Antioxidant Applications:
The hydroxy-phenyl group in [4-(2-Hydroxy-phenyl)-[1,2,5]thiadiazol-3-yl]-morpholin-4-yl-methanone suggests its potential use as an antioxidant or radical scavenger. This application can be beneficial in the development of products that protect cells from oxidative stress and damage, which is a common factor in many diseases and aging processes.
Used in Drug Delivery Systems:
Similar to gallotannin, [4-(2-Hydroxy-phenyl)-[1,2,5]thiadiazol-3-yl]-morpholin-4-yl-methanone can be employed in the development of novel drug delivery systems. These systems can improve the compound's delivery, bioavailability, and therapeutic outcomes, making it a valuable component in the design of advanced pharmaceutical formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 119458-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,5 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119458-67:
(8*1)+(7*1)+(6*9)+(5*4)+(4*5)+(3*8)+(2*6)+(1*7)=152
152 % 10 = 2
So 119458-67-2 is a valid CAS Registry Number.
119458-67-2Relevant academic research and scientific papers
Synthesis of 4H-Benzopyranothiadiazol-4-one and Its Reactions with Some Nucleophilic and Electrophilic Agents
Savel'ev, V. L.,Samsonova, O. L.,Troitskaya, V. S.,Vinokurov, V. G.,Lezina, V. P.,Smirnov, L. D.
, p. 805 - 810 (2007/10/02)
The reaction of 3,4-diaminocoumarin with thionyl chloride gave 4H-benzopyranothiodiazol-4-one (II), which was cleaved by the action of nucleophilic agents to the corresponding 4-(2-hydroxyphenyl)-1,2,5-thiadiazole-3-carboxylic acid derivatives.The nitration of II leads to the 8-nitro or 6,8-dinitro derivative; the latter was isolated in the form of 4-(2-hydroxy-3,5-dinitrophenyl)-1,2,5-thiadiazole-3-carboxylic acid.
