Molecular Formula (分子式):

C15H15N

Molecular Weight (分子量)：

209.29

Purity (纯度):

99%

Specification:(指标)

MS, HNMR, Purity 99%

Contact Telephone (联系电话):

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Structure (结构式):

功能：

• OLED 与有机光电材料的合成羟基（-OH）和溴（-Br）是两类高活性反应位点：

• 溴原子可通过 ** 铃木反应（Suzuki-Miyaura）、根岸反应（Negishi）** 等过渡金属催化偶联反应，引入芳基、杂芳基等共轭基团，构建大 π 共轭体系；

• 羟基可发生酯化、醚化反应，或进一步转化为离去基团，用于修饰分子的溶解性、成膜性。基于该化合物合成的衍生物，可作为OLED 发光层材料、空穴传输材料的前体，尤其适用于蓝光或深蓝光发光器件的研发，提升器件的发光效率和稳定性。

• 有机半导体与电子材料研发二苯并呋喃母核具有良好的平面共轭结构和电荷传输性能，溴代和羟基化修饰后，可调控分子的前线轨道能级（HOMO/LUMO）。其衍生物可用于制备有机场效应晶体管（OFET）的半导体层材料、有机光伏电池（OPV）的受体或给体材料，优化器件的电荷迁移率和光电转换效率。

• 医药与生物活性分子的合成砌块二苯并呋喃骨架是多种天然产物和药物分子的核心结构，具有抗炎、抗菌、抗肿瘤等潜在生物活性。9 - 溴 - 2 - 羟基二苯并呋喃可通过官能团转化，引入靶向基团或药效团，用于新型杂环药物分子的设计与合成，尤其是抗真菌、抗肿瘤药物的先导化合物筛选。

• 高性能聚合物单体该化合物可作为单体参与缩聚反应，例如与二卤代芳烃发生亲核取代缩聚，或与含炔基化合物发生点击化学聚合，制备含二苯并呋喃单元的耐高温聚合物、光电功能高分子材料，这类聚合物可用于特种涂料、柔性电子器件基板等领域。

Function：

• Synthesis of OLED and organic optoelectronic materialsThe hydroxyl (-OH) and bromine (-Br) groups serve as two highly reactive sites:

• The bromine atom can be used to introduce aryl, heteroaryl, and other conjugated groups via transition metal-catalyzed coupling reactions such as the Suzuki-Miyaura reaction and Negishi reaction, constructing large π-conjugated systems.

• The hydroxyl group can undergo esterification, etherification, or be further converted into a leaving group to modify the solubility and film-forming properties of molecules.Derivatives synthesized from this compound can act as precursors for OLED emissive layer materials and hole transport materials, particularly suitable for the development of blue or deep-blue light-emitting devices, enhancing their luminous efficiency and stability.

• R&D of organic semiconductors and electronic materialsThe dibenzofuran core features an excellent planar conjugated structure and charge transport performance. Modification with bromination and hydroxylation can regulate the frontier orbital energy levels (HOMO/LUMO) of molecules.Its derivatives can be used to fabricate semiconductor layer materials for organic field-effect transistors (OFETs) and acceptor or donor materials for organic photovoltaic cells (OPVs), optimizing the charge mobility and photoelectric conversion efficiency of devices.

• Building block for pharmaceutical and bioactive moleculesThe dibenzofuran skeleton is the core structure of various natural products and pharmaceutical molecules, exhibiting potential bioactivities such as anti-inflammatory, antibacterial, and antitumor effects.9-Bromo-2-hydroxydibenzofuran can be modified with targeted or pharmacophoric groups through functional group transformation, facilitating the design and synthesis of novel heterocyclic pharmaceutical molecules, especially the screening of lead compounds for antifungal and antitumor drugs.

• Monomer for high-performance polymersThis compound can serve as a monomer in polycondensation reactions—for instance, nucleophilic substitution polycondensation with dihaloarenes, or click chemistry polymerization with alkynyl-containing compounds—to prepare high-temperature resistant polymers and optoelectronic functional polymer materials with dibenzofuran units. Such polymers are applicable in specialty coatings, substrates for flexible electronic devices, and other fields.

• Summary: The core value of this compound stems from its dual reactive functional groups (bromine + hydroxyl) and conjugated heterocyclic core. It acts as a key intermediate bridging basic chemical raw materials and high-end optoelectronic/pharmaceutical materials, boasting irreplaceable application potential in high-tech fields including organic electronics, new materials, and pharmaceutical R&D.