CAS 6969-71-7
:1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one
Description:
1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one, with the CAS number 6969-71-7, is a heterocyclic compound featuring a fused triazole and pyridine ring system. This compound is characterized by its unique structural framework, which includes a triazole ring that contributes to its potential biological activity. It typically exhibits properties such as moderate solubility in polar solvents and may possess acidic or basic characteristics depending on the functional groups present. The presence of the triazole moiety often imparts interesting pharmacological properties, making it a subject of interest in medicinal chemistry for its potential applications in drug development. Additionally, this compound may participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, due to the reactivity of its nitrogen atoms. Its derivatives are often explored for their roles in various therapeutic areas, including anti-inflammatory and antimicrobial activities. Overall, 1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one represents a versatile scaffold in organic synthesis and medicinal chemistry.
Formula:C6H5N3O
InChI:InChI=1/C6H5N3O/c10-6-8-7-5-3-1-2-4-9(5)6/h1-4H,(H,8,10)
InChI key:InChIKey=LJRXNXBFJXXRNQ-UHFFFAOYSA-N
SMILES:O=C1N2C(C=CC=C2)=NN1
Synonyms:- 1,2,4-Triazolo-[4,3-a]-Pyridine-3(2H)-One
- 1,2,4-triazolo-4,3-pyridin-3(2H)-one
- 1,2,4-trizolo(4,3a)pyridin-3(2H)-one
- 2H,3H-[1,2,4]Triazolo[4,3-a]pyridin-3-one
- 2H-[1,2,4]Triazolo[4,3-a]pyridin-3-one
- 3-Hydroxytriazolo[4,3-a]pyridine
- NSC 68462
- [1,2,4]Triazolo[4,3-a]pyridin-3-ol
- s-Triazolo[4,3-a]pyridin-3-ol
- 1,2,4-Triazolo(4,3-a)-pyridin-3(2H)-one
- [1,2,4]triazolo[4,3-a]pyridin-3(2H)-one
- 1,2,4-triazolo[4,3-a]pyridin-3(2H)one
- 1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one
- 1,2,4-Triazole-(4,3-alpha)pyri
- 1,2,4-Triazolopyridin-3-one
- 1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one, 98+%
- 1,2,4-Triazole-(4,3-a) Pyridine-3 (2H)-One
- 3-HYDROXY-1,2,4-TRIAZOLO[4,3-A]PYRIDINE
- 1,2,4-TRIAZOLE(4,3)PYRIDIN-3-(2H)-ONE
- 1,2,4-TRIAZOL-(4,3-A)-PYRIDINE 3 (2H)-ONE
- See more synonyms
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Found 10 products.
1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one
CAS:Formula:C6H5N3OPurity:>98.0%(T)(HPLC)Color and Shape:White to Green to Brown powder to crystalMolecular weight:135.131,2,4-Triazolo[4,3-a]pyridin-3(2H)-one, 98+%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C6H5N3OPurity:98+%Color and Shape:White to cream, Crystals or powder or crystalline powderMolecular weight:135.131,2,4-Triazolo[4,3-a]pyridin-3(2H)-one
CAS:Formula:C6H5N3OPurity:98%Color and Shape:SolidMolecular weight:135.1234Trazodone EP Impurity K (Triazolopyridinone)
CAS:Formula:C6H5N3OColor and Shape:Off-White SolidMolecular weight:135.131,2,4-Triazolo[4,3-a]pyridine-3(2H)-one
CAS:Controlled ProductFormula:C6H5N3OColor and Shape:NeatMolecular weight:135.12[1,2,4]Triazolo[4,3-a]pyridin-3-ol
CAS:<p>[1,2,4]Triazolo[4,3-a]pyridin-3-ol</p>Purity:98%Molecular weight:135.12g/mol1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one
CAS:Controlled Product<p>Applications 1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one was used to prepare a congener of Trazodone (T718500) which was found to be a potent and selective inhibitor of synaptosomal uptake of 5-hydroxytryptamine.<br>References Alhaider, A.A.: J. Pharmac. Sci., 81, 99 (1992);<br></p>Formula:C6H5N3OColor and Shape:NeatMolecular weight:135.12[1,2,4]Triazolo[4,3-a]pyridin-3(2H)-one
CAS:Formula:C6H5N3OPurity:98%Color and Shape:SolidMolecular weight:135.1261,2,4-Triazolo[4,3-a]pyridin-3(2H)-one
CAS:<p>1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one is a potent inhibitor of the enzyme c-glycosylase. This compound has been used in pharmaceutical preparations and as a feedstock in organic syntheses. It is used to produce the anti-inflammatory drug piroxicam, which inhibits the action of cyclooxygenase and blocks the synthesis of prostaglandins. 1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one also has been shown to inhibit crystallization of the bovine liver enzyme phosphatidylcholine:cholesterol acyltransferase (PCAT). The inhibition was found to be competitive with respect to PCAT substrate and was not due to inhibition of PCAT by 1,2,4-triazolo[4,3-a]pyridin-3(</p>Formula:C6H5N3OPurity:Min. 95%Molecular weight:135.13 g/mol









