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HS Code |
196401 |
| Chemical Name | 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene |
| Molecular Formula | C20H15NS |
| Molecular Weight | 301.41 |
| Cas Number | Unknown |
| Appearance | Solid (presumed, as typical for aromatic amines) |
| Structure | Biphenyl substituted benzo[b]thiophene with para-amino group |
| Smiles | Nc1ccc(cc1)c2ccc3ccccc3s2 |
| Inchi | InChI=1S/C20H15NS/c21-17-9-12-19(13-10-17)18-8-7-15-5-1-2-6-16(15)22-20(18)14-11-19 |
As an accredited 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 1-gram amber glass vial, sealed with a PTFE-lined cap, and labeled with product details and safety icons. |
| Shipping | The chemical 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene is shipped in tightly sealed containers under inert atmosphere, protected from light and moisture. Packaging complies with relevant chemical transport regulations to ensure safety. Proper labeling and documentation are included, and temperature control may be provided if required. Handle with appropriate precautions during receiving and storage. |
| Storage | Store 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to incompatible substances such as strong oxidizing agents. Use proper personal protective equipment when handling. Label the storage container clearly, following standard laboratory chemical storage guidelines. |
Applications of 2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene in Industrial Manufacturing2-(4-Aminobiphenyl-4-yl)benzo[b]thiophene, as manufactured in our advanced production facility, serves key roles in several specialty chemical sectors, focusing on advanced material synthesis and high-value intermediate manufacturing. Below are distinct downstream industrial scenarios detailing technical application practices aligned with compliance and quality systems. 1. Organic Semiconductor Material SynthesisThis compound acts as a core building block in the synthesis of organic semiconductors used in thin-film transistors, OLED displays, and photovoltaic devices. Its electron-rich structure supports efficient charge transport when integrated into polymer backbones or small-molecule systems. Manufacturers incorporate it through direct arylation polymerization or Suzuki coupling step to achieve the desired electronic properties. Industry compliance standards
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2. Specialty Dye and Pigment IntermediateDownstream dye and pigment manufacturers utilize this molecule as a key intermediate in synthesizing high-performance dyes for electronic inks, industrial coatings, and laser marking applications. Its biphenyl-aminothiophene motif attaches to chromophore systems to enhance absorption and light stability under extreme processing and use conditions. Industry compliance standards
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3. Pharmaceutical Research IntermediatePharmaceutical innovators deploy this compound as a research intermediate for synthesizing new heterocyclic drug candidates, specifically targeting oncology and CNS indications. Its structure facilitates biaryl and thieno scaffold construction, critical for library diversification in medicinal chemistry workflows. Researchers may further derivatize it via amide coupling or cyclization to access advanced lead compounds. Industry compliance standards
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4. Advanced Polymer Additive for Engineering PlasticsEngineering polymer producers integrate this molecule as a reactive additive to modify optical, electronic, or mechanical properties in high-performance resins such as polyimides, polyesters, or polysulfones. Its presence can introduce pi-conjugated segments or functional sites, enhancing processability or imparting specific UV- and heat-resistance characteristics demanded in automotive, aerospace, and electronics markets. Industry compliance standards
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