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4-CYCLOHEXYL-5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is a chemical compound belonging to the triazole family, characterized by a molecular formula of C13H16N4S. It features a unique structure with a five-membered ring composed of sulfur and nitrogen atoms, and a cyclohexyl and pyridinyl group attached to it. 4-CYCLOHEXYL-5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is known for its diverse range of biological activities and is widely studied in the fields of medicinal chemistry and pharmaceuticals.

23714-52-5

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23714-52-5 Usage

Uses

Used in Pharmaceutical Industry:
4-CYCLOHEXYL-5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is used as a potential anti-cancer agent for its ability to target and inhibit the growth of cancer cells. It has been studied for its potential to treat various types of cancer due to its ability to interfere with essential cellular processes in cancer cells.
4-CYCLOHEXYL-5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is also used as an anti-inflammatory agent, leveraging its capacity to reduce inflammation and alleviate pain associated with various conditions. Its anti-inflammatory properties make it a promising candidate for the development of new medications to treat inflammatory diseases.
In the field of anti-fungal agents, 4-CYCLOHEXYL-5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is used to combat fungal infections by inhibiting the growth and proliferation of fungi, making it a potential candidate for the development of new anti-fungal drugs.
4-CYCLOHEXYL-5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is used as an enzyme inhibitor, targeting specific enzymes involved in various biological processes. Its ability to inhibit these enzymes makes it a valuable tool in the development of drugs for treating enzyme-related disorders.
Furthermore, 4-CYCLOHEXYL-5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is being investigated for its potential role in the treatment of neurological disorders. Its neuroprotective properties and ability to modulate neuronal function make it a promising candidate for the development of therapies to address neurological conditions.
Overall, 4-CYCLOHEXYL-5-PYRIDIN-4-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is a versatile and promising compound with a wide range of potential applications in the field of medicine and drug development, offering new avenues for the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 23714-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,1 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23714-52:
(7*2)+(6*3)+(5*7)+(4*1)+(3*4)+(2*5)+(1*2)=95
95 % 10 = 5
So 23714-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N4S/c18-13-16-15-12(10-6-8-14-9-7-10)17(13)11-4-2-1-3-5-11/h6-9,11H,1-5H2,(H,16,18)

23714-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-cyclohexyl-3-pyridin-4-yl-1H-1,2,4-triazole-5-thione

1.2 Other means of identification

Product number -
Other names 4-Cyclohexyl-5-pyridin-4-yl-4H-[1,2,4]triazole-3-thiol

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:23714-52-5 SDS

23714-52-5Relevant academic research and scientific papers

Narrow SAR in odorant sensing Orco receptor agonists

Romaine, Ian M.,Taylor, Robert W.,Saidu, Samsudeen P.,Kim, Kwangho,Sulikowski, Gary A.,Zwiebel, Laurence J.,Waterson, Alex G.

, p. 2613 - 2616 (2015/02/19)

The systematic exploration of a series of triazole-based agonists of the cation channel insect odorant receptor is reported. The structure-activity relationships of independent sections of the molecules are examined. Very small changes to the compound structure were found to exert a large impact on compound activity. Optimal substitutions were combined using a 'mix-and-match' strategy to produce best-in-class compounds that are capable of potently agonizing odorant receptor activity and may form the basis for the identification of a new mode of insect behavior modification.

Narrow SAR in odorant sensing Orco receptor agonists

Romaine, Ian M.,Taylor, Robert W.,Saidu, Samsudeen P.,Kim, Kwangho,Sulikowski, Gary A.,Zwiebel, Laurence J.,Waterson, Alex G.

, p. 2613 - 2616 (2014/06/09)

The systematic exploration of a series of triazole-based agonists of the cation channel insect odorant receptor is reported. The structure-activity relationships of independent sections of the molecules are examined. Very small changes to the compound structure were found to exert a large impact on compound activity. Optimal substitutions were combined using a 'mix-and-match' strategy to produce best-in-class compounds that are capable of potently agonizing odorant receptor activity and may form the basis for the identification of a new mode of insect behavior modification.

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