Product Description
Cigna Qingdao is mainly engaged in the intermediates of febuxostatin, ceflothrin, eprazole, flubiprofen, phenalidone, tovaptan, rivaroxaban and Avanafil, terbinafine intermediates, thioacetamide and thiophene and their derivatives.
AI Product Description
*The following content is generated by AI and is for reference only.
The chemical compound known as (2-Butyl-5-nitro-3-benzofuranyl)[4-[3-(dibutylamino)propoxy]phenyl]methanone represents a sophisticated heterocyclic ketone designed for advanced pharmaceutical and agrochemical research. While specific commercial availability may vary, this molecule is structurally characterized by a benzofuran core substituted with a nitro group at the 5-position and a butyl chain at the 2-position. Attached to the 3-position of the furan ring is a methanone bridge connecting to a phenyl ring, which itself bears a propoxy side chain terminated by a dibutylamino group. This unique architecture combines electron-withdrawing nitro functionality with lipophilic alkyl chains and a basic amine center, properties often sought in drug discovery to modulate membrane permeability and receptor binding affinity.
Currently, no widely recognized CAS number is publicly associated with this exact complex structure in major global chemical databases such as PubChem or SciFinder, suggesting it may be an intermediate in proprietary synthesis or a specialized research reagent not yet assigned a standard registry identifier. Its primary application lies within medicinal chemistry laboratories where it serves as a scaffold for developing novel bioactive agents. The nitrobenzofuran motif is frequently investigated for potential anticancer, antimicrobial, or anti-inflammatory activities due to its ability to interact with specific biological targets. Meanwhile, the long-chain dialkylamine moiety enhances solubility profiles and facilitates interactions with hydrophobic pockets in enzyme active sites. Researchers utilize such compounds to explore structure-activity relationships (SAR), aiming to optimize potency while minimizing toxicity. In agricultural science, similar structural frameworks are occasionally evaluated for their efficacy as growth regulators or pest control agents, though data on this specific derivative remains limited to academic literature. Due to the presence of the nitro group, handling requires strict safety protocols regarding potential mutagenicity and environmental persistence. Overall, this molecule exemplifies the complexity of modern organic synthesis aimed at creating highly selective therapeutic candidates, serving as a critical tool for scientists pushing the boundaries of chemical biology and pharmacology.