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(5E)-5-(5-bromo-3-phenyl-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is a novel triazoline derivative characterized by its triazolidine-3-thione molecular scaffold and the presence of phenyl and bromo-substituted indole groups. This chemical compound holds promise for pharmaceutical and biological applications due to its potential for a broad spectrum of pharmacological activities.

126016-45-3

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126016-45-3 Usage

Uses

Used in Pharmaceutical Industry:
(5E)-5-(5-bromo-3-phenyl-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is used as a potential candidate for drug discovery and development. Its unique structural features, including the triazolidine-3-thione scaffold and the phenyl and bromo-substituted indole groups, contribute to its potential for a wide range of pharmacological activities.
Used in Antimicrobial Applications:
In the field of antimicrobial research, (5E)-5-(5-bromo-3-phenyl-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is used as an antimicrobial agent. Its structural components suggest that it may exhibit properties effective against various microorganisms, making it a valuable compound for further investigation in this area.
Used in Antifungal Applications:
(5E)-5-(5-bromo-3-phenyl-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is also used as an antifungal agent. (5E)-5-(5-bromo-3-phenyl-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione's potential to combat fungal infections is of interest to researchers, as it may lead to the development of new antifungal drugs.
Used in Anticancer Applications:
Within the oncology sector, (5E)-5-(5-bromo-3-phenyl-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione is used as an anticancer agent. Its potential to exhibit anticancer properties makes it a promising compound for further research and development in the fight against cancer.
Further research is necessary to fully understand the chemical and biological properties of (5E)-5-(5-bromo-3-phenyl-2H-indol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione and to explore its potential applications in medicine and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 126016-45-3 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 126016-45:
(8*1)+(7*2)+(6*6)+(5*0)+(4*1)+(3*6)+(2*4)+(1*5)=93
93 % 10 = 3
So 126016-45-3 is a valid CAS Registry Number.

126016-45-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(5-bromo-3-phenylindol-2-ylidene)-4-phenyl-1,2,4-triazolidine-3-thione

1.2 Other means of identification

Product number -
Other names 5-bromo-3-phenyl-2-(5'-mercapto-4'-phenyl-1',2',4'-triazol-3'-yl)indole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:126016-45-3 SDS

126016-45-3Downstream Products

126016-45-3Relevant 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-

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