29552-52-1 Usage
Description
4-ETHYL-5-(4-FLUOROPHENYL)-1,2,4-TRIAZOLE-3-THIOL is a chemical compound with the molecular formula C11H10F3N3S. It is a triazole derivative featuring a substituted phenyl and ethyl group, along with a fluorine atom. 4-ETHYL-5-(4-FLUOROPHENYL)-1,2,4-TRIAZOLE-3-THIOL is known for its potential applications in medicinal and agricultural chemistry due to the diverse biological activities of triazoles, such as antifungal, antiviral, and anticancer properties. The presence of the thiol group also indicates its potential reactivity in organic synthesis and material science. Further research is necessary to fully explore the properties and potential uses of this compound.
Uses
Used in Medicinal Chemistry:
4-ETHYL-5-(4-FLUOROPHENYL)-1,2,4-TRIAZOLE-3-THIOL is used as a pharmaceutical candidate for its potential antifungal, antiviral, and anticancer properties. The triazole structure is known to exhibit a wide range of biological activities, making it a valuable component in the development of new drugs.
Used in Agricultural Chemistry:
In the agricultural industry, 4-ETHYL-5-(4-FLUOROPHENYL)-1,2,4-TRIAZOLE-3-THIOL is used as a potential bioactive agent for controlling fungal infections in crops. Its antifungal properties can contribute to the development of new agrochemicals to protect plants from diseases.
Used in Organic Synthesis:
4-ETHYL-5-(4-FLUOROPHENYL)-1,2,4-TRIAZOLE-3-THIOL is used as a reactive intermediate in organic synthesis due to the presence of the thiol group. This group can participate in various chemical reactions, such as nucleophilic substitutions and redox reactions, making it a useful building block for the synthesis of more complex molecules.
Used in Material Science:
In the field of material science, 4-ETHYL-5-(4-FLUOROPHENYL)-1,2,4-TRIAZOLE-3-THIOL is used for its potential to form new materials with unique properties. The combination of the triazole ring and the thiol group can lead to the development of novel materials with applications in various industries, such as electronics, coatings, and adhesives. Further research is required to explore the full potential of this compound in material science.
Check Digit Verification of cas no
The CAS Registry Mumber 29552-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29552-52:
(7*2)+(6*9)+(5*5)+(4*5)+(3*2)+(2*5)+(1*2)=131
131 % 10 = 1
So 29552-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H10FN3S/c1-2-14-9(12-13-10(14)15)7-3-5-8(11)6-4-7/h3-6H,2H2,1H3,(H,13,15)
29552-52-1Relevant articles and documents
COMPOUNDS FOR MODULATING AQUAPORINS
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Page/Page column 32; 33-34, (2017/12/08)
The invention relates to compounds of formula (I) pharmaceutical compositions thereof and methods for modulating aquaporin 9.
Evaluation of antimycobacterial and anticonvulsant activities of new 1- (4-fluorobenzoyl)-4-substituted-thiosemicarbazide and 5-(4-fluorophenyl)-4- substituted-2,4-dihydro-3H,1,2,4-triazole-3-thione derivatives
Gulerman,Rollas
, p. 691 - 695 (2007/10/03)
Some new 1-(4-fluorobenzoyl)-4-alkyl/arylthiosemicarbazide (2a-g), 5- (4-fluorophenyl)4-alkyl/aryl-2,4-dihydr-3H-1,2,4-triazole-3-thione (3a-g) derivatives, 3-(benzylthio)-5-(4-fluorophenyl)-4-phenyl-4H-1,2,4-triazole (3h) and 2-acetyl-5-(4-fluorophenyl)-
