452105-55-4

Basic information

• Product Name: (Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate
• Synonyms: (Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate
• CAS NO: 452105-55-4
• Molecular Weight: 418.387
• Mol File: 452105-55-4.mol
• Article Data: 0

Chemical Properties

• Density: 1.58±0.1 g/cm3(Predicted)
• CAS DataBase Reference: (Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate(452105-55-4)
• EPA Substance Registry System: (Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate(452105-55-4)

Safety Data

• Hazardous Substances Data: 452105-55-4(Hazardous Substances Data)

Usage

Description

(Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate is a complex organic molecule with a unique structure that features a pyridine ring fused with a triazolo ring. This structure is attached to a pyrrole ring that is substituted with a carboxylate group. The molecule also contains a 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl) group, which is a derivative of indolin-3-ylidene and is bonded to the pyridin-3-yl moiety. The (Z) configuration of the compound suggests that the substituents on the double bond are on the same side of the molecule. This specific arrangement and the compound's structure imply potential pharmaceutical or biological activity, as similar compounds are often found to have drug-like properties. They may be utilized in medicinal or research settings for their therapeutic effects.

Uses

Used in Pharmaceutical Industry:
(Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate is used as a potential therapeutic agent for various medical conditions due to its complex structure and potential biological activity. (Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate's specific arrangement and functional groups may allow it to interact with biological targets, such as receptors or enzymes, which could lead to the development of new treatments for diseases.
Used in Research and Development:
In the field of research and development, (Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate can be used as a starting point for the synthesis of new compounds with potential applications in medicine. Its unique structure may serve as a basis for the design of novel drugs or for studying the interactions between molecules and their biological targets.
Used in Drug Design and Medicinal Chemistry:
(Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate is used as a structural template in drug design and medicinal chemistry. Its specific arrangement of functional groups and rings can be modified to create a series of related compounds with varying biological activities. This allows researchers to optimize the compound's properties, such as its potency, selectivity, and pharmacokinetics, to improve its therapeutic potential.
Used in Chemical Synthesis:
(Z)-3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl 5-((5-fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylate can also be used as an intermediate in the synthesis of other complex organic molecules. Its unique structure and functional groups make it a valuable building block for the creation of novel compounds with a wide range of applications, from pharmaceuticals to materials science.

Downstream Products

• 557795-19-4 sunitinib 
• 341031-54-7 sunitinib malate