126016-44-2 Usage
Uses
Used in Medicinal Chemistry:
(5Z)-5-(5-bromo-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is used as a building block for the development of novel pharmaceutical compounds due to its unique molecular structure and the presence of bioactive functional groups. (5Z)-5-(5-bromo-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione's heterocyclic nature and the potential for molecular interactions make it a promising candidate for the design of new drugs targeting various diseases.
Used in Material Science:
In the field of material science, (5Z)-5-(5-bromo-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is used as a component in the synthesis of advanced materials with specific properties. (5Z)-5-(5-bromo-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione's structural features, such as the 1,2,4-triazolidine ring and the bromo and phenyl substituents, may contribute to the development of materials with tailored characteristics for applications in electronics, sensors, or other high-tech industries.
Used in Chemical Research:
(5Z)-5-(5-bromo-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione serves as a subject of study in chemical research, where its reactivity, stability, and interaction with other molecules can be investigated. Understanding the compound's behavior in various chemical reactions can lead to the discovery of new synthetic pathways and the development of innovative applications in both academia and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 126016-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,1 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126016-44:
(8*1)+(7*2)+(6*6)+(5*0)+(4*1)+(3*6)+(2*4)+(1*4)=92
92 % 10 = 2
So 126016-44-2 is a valid CAS Registry Number.
126016-44-2Relevant academic research and scientific papers
Synthesis of oxadiazolyl-, thiadiazolyl- and triazolylindoles and indolylthiazolidinones
Hiremath, S. P.,Sonar, V. N.,Raja Sekhar, K.,Purohit, M. G.
, p. 626 - 630 (2007/10/02)
Ethyl substituted indole-2-carboxylates (1a-n) are reacted with hydrazine hydrate to get the corresponding carbohydrazides (2a-n).These hydrazides are condensed with phenyl isothiocyanate to get 1-phenyl-3-(substituted indole-2'-carboxamido)thioureas (3a-
