126016-36-2 Usage
Uses
Used in Pharmaceutical Applications:
(5Z)-5-(5-chloro-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is used as a pharmaceutical compound for its potential therapeutic effects. Its specific application reason is attributed to its unique chemical structure and properties, which may contribute to its efficacy in treating certain medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (5Z)-5-(5-chloro-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is used as a research compound for studying its biological activities and exploring its potential as a drug candidate. (5Z)-5-(5-chloro-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione's structural features and chemical properties make it an interesting subject for further investigation and development.
Used in Drug Development:
(5Z)-5-(5-chloro-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is utilized as a starting point in drug development, where its unique structure and potential pharmaceutical applications are leveraged to design and synthesize new drugs with improved efficacy and safety profiles. (5Z)-5-(5-chloro-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione's properties may be harnessed to address specific medical needs or to overcome existing challenges in drug therapy.
Check Digit Verification of cas no
The CAS Registry Mumber 126016-36-2 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, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 126016-36:
(8*1)+(7*2)+(6*6)+(5*0)+(4*1)+(3*6)+(2*3)+(1*6)=92
92 % 10 = 2
So 126016-36-2 is a valid CAS Registry Number.
126016-36-2Relevant 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-
