9-chloronaphtho[2,1-b]benzofuran
2379460-04-3
>99%
light white powder
Handan City,Hebei Province, China
Hebei Huaqing Optoelectronics focuses on the research and production of OLED materials.
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*The following content is generated by AI and is for reference only.
9-Chloronaphtho[2,1-b]benzofuran is a specialized heterocyclic organic compound characterized by a fused tricyclic framework consisting of naphthalene and benzofuran units, with a chlorine atom substituted at the ninth position. While specific commercial data for this exact molecule may be limited in public databases due to its niche status as a research intermediate rather than a mass-market commodity, its structural class places it within the realm of polycyclic aromatic ethers used primarily in advanced chemical synthesis. The molecular formula is typically C16H9ClO, corresponding to a molecular weight of approximately 252.70 g/mol. Its CAS registry number is not widely listed in standard global catalogs like PubChem or ChemSpider under common search terms, suggesting it may be a proprietary intermediate or a specific derivative synthesized for targeted studies in materials science or medicinal chemistry.
In industrial and academic applications, compounds of this nature serve as critical building blocks for the development of functional organic materials. The rigid, planar structure of the naphtho-benzofuran core contributes to excellent thermal stability and unique electronic properties, making it highly valuable for the synthesis of organic light-emitting diodes (OLEDs), fluorescent probes, and high-performance polymers. The presence of the chlorine substituent offers a versatile site for further chemical modification through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, allowing chemists to attach diverse functional groups to tune solubility, band gaps, or biological activity. Consequently, this molecule is predominantly utilized in pharmaceutical research as a scaffold for designing novel bioactive agents targeting specific receptors or enzymes. It also finds application in the field of agrochemicals, where similar fused heterocycles exhibit pesticidal or herbicidal properties. Due to its complexity, 9-chloronaphtho[2,1-b]benzofuran is generally produced via multi-step synthetic routes involving cyclization and halogenation, often handled under strict safety protocols given the potential toxicity associated with halogenated aromatic compounds. Researchers rely on this compound to explore new frontiers in organic electronics and drug discovery, leveraging its unique architecture to create next-generation technologies with superior performance characteristics compared to traditional linear analogs.