1186651-51-3 | (Z)-5-((5-Fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide

Packsize	Purity	Availability	Price	Discounted Price
50mg	98%	in stock	$278.00	$195.00
100mg	98%	in stock	$448.00	$314.00

Description

• Catalog Number: AE11599
• Chemical Name: (Z)-5-((5-Fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide
• CAS Number: 1186651-51-3
• Molecular Formula: C27H44N10O6
• Molecular Weight: 604.7017
• MDL Number: MFCD21496432
• SMILES: O=CC(N(C(=O)[C@@H](NC(=O)NC(C(=O)O)Cc1ccccc1)CCCNC(=N)N)[C@H](C(=O)N)C(C)C)CCCNC(=N)N

Upstream Synthesis Route

(Z)-5-((5-Fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide, often referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable tool in the development of complex organic compounds.In chemical synthesis, $name$ can be utilized as a key intermediate in the construction of various heterocyclic compounds, pharmaceuticals, agrochemicals, and functional materials. Its ability to undergo diverse chemical transformations, such as cross-coupling reactions, cycloadditions, and condensations, allows for the efficient and selective formation of new carbon-carbon and carbon-nitrogen bonds.Furthermore, the presence of the indolin-3-ylidene moiety in $name$ makes it a potent nucleophilic center, enabling it to participate in important reactions like nucleophilic addition, substitution, and ring-closure reactions. This reactivity profile opens up avenues for the regioselective and stereoselective synthesis of complex molecules with defined structures and properties.Overall, the strategic incorporation of (Z)-5-((5-Fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide in chemical synthesis facilitates the efficient construction of diverse chemical entities with potential applications in drug discovery, material science, and other fields requiring tailored molecular design.