77803-56-6 Usage
Description
[5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid is a complex organic molecule characterized by the presence of a benzodioxol ring, a triazol ring, and a thiol group attached to an acetic acid moiety. This unique structure endows the compound with potential applications in various scientific fields due to its chemical reactivity and the possibility of binding to metal ions.
Uses
Used in Organic Synthesis:
[5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid is used as a building block in organic synthesis for creating a diverse range of complex organic compounds. The presence of the benzodioxol and triazol rings, along with the thiol group, provides a versatile platform for the development of novel molecules with specific properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid is used as a pharmacophore in drug design. Its structural features make it a promising candidate for the development of new drugs, particularly those targeting specific biological receptors or enzymes.
Used in Medicinal Chemistry:
[5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid is utilized in medicinal chemistry for the investigation of its potential therapeutic properties. [5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid's ability to interact with metal ions and its reactivity may contribute to its efficacy in treating certain medical conditions.
Used in Biochemistry:
In biochemistry, [5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid is used to study its interactions with biological macromolecules, such as proteins and nucleic acids. Understanding these interactions can provide insights into the compound's potential roles in biological processes and its applicability in the development of bioactive molecules.
Used in Materials Science:
[5-(1,3-benzodioxol-5-yl)-1H-1,2,4-triazol-3-yl]sulfanylacetic acid may also find applications in materials science, where its unique structural features could be exploited to create new materials with specific properties, such as improved conductivity or enhanced stability.
Check Digit Verification of cas no
The CAS Registry Mumber 77803-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,0 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77803-56:
(7*7)+(6*7)+(5*8)+(4*0)+(3*3)+(2*5)+(1*6)=156
156 % 10 = 6
So 77803-56-6 is a valid CAS Registry Number.
77803-56-6Relevant articles and documents
Synthesis of carboxyalkylthio-triazoles and bicyclic derivatives with antiinflammatory and analgesic activity
Mazzone,Pignatello,Mazzone,Panico,Barbera,Catti,Chiechio,Arrigo-Reina,Castorina,Russo
, p. 149 - 169 (2007/10/02)
3-Carboxyalkylthio derivatives of 5-alkoxyphenyl-1,2,4-triazole were prepared, performing some substitutions both on carboxyalkyl chain, by lengthening it or introducing substituents with increasing molecular weight in α- at the carboxy group, and on N-4
