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HS Code |
960809 |
| Product Name | 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile |
| Cas Number | 1337532-29-4 |
| Molecular Formula | C13H10F3NOS2 |
| Molecular Weight | 317.35 |
| Appearance | Yellow solid |
| Purity | ≥98% |
| Melting Point | 101-104°C |
| Solubility | Soluble in DMSO, DMF |
| Storage Temperature | 2-8°C |
| Smiles | CCS(=C(C#N)C(=O)C1=CC(=CC=C1)C(F)(F)F)SC |
| Inchi | InChI=1S/C13H10F3NOS2/c1-19-13(20-2)11(7-17)12(18)8-3-4-10(5-6-8)9(14,15)16/h3-6H,1-2H3 |
As an accredited 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 25g amber glass bottle with a secure cap, featuring a clear chemical label and appropriate hazard warnings. |
| Shipping | The chemical 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile should be shipped in tightly sealed, chemical-resistant containers, under cool, dry conditions. Package and label per hazardous materials regulations, avoiding exposure to heat, moisture, and incompatible substances. Handle with care and ensure all documentation complies with relevant local and international transport guidelines. |
| Storage | Store **3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Properly label storage containers and ensure they remain protected from moisture and physical damage. Use appropriate personal protective equipment when handling. |
Applications of 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile in Industrial ManufacturingWe supply 3,3-Bis(Methylthio)-2-[3-(Trifluoromethyl)Benzoyl]Acrylonitrile as a specialty raw material for advanced chemical synthesis. The following sectors represent current routes of substantial industrial consumption. 1. Pharmaceutical Intermediate SynthesisMajor pharmaceutical companies and CMOs apply this compound as a protected building block for synthesizing selective kinase inhibitors and receptor modulators. Its unique structure enables regioselective coupling in step-growth routes, supporting assembly of advanced drug candidates in oncology and CNS research pipelines. Controlled addition into the reaction batch reduces side-product formation and allows precise downstream purification. Regulatory review demands consistent batch traceability and impurity documentation across all synthesis stages. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Fungicide Precursors)Leading crop science firms incorporate this compound into formulations of advanced herbicide and fungicide precursors, targeting more selective weed or pathogen control. Because it can introduce both methylthio and trifluoromethyl moieties, formulators enhance bioactivity while reducing environmental persistence. Usage requires compliance with registration dossiers and controlled toxicological evaluation. Industry compliance standards
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3. Specialty Dye and Pigment ManufacturingIndustrial colorant manufacturers use this chemical as a functionalized intermediate in high-storage-stability dyes. Its structural motifs facilitate the introduction of electron-withdrawing groups, thereby raising colorfastness and resistance to photobleaching. Integration into pigment blending occurs at the pre-condensation stage, supporting production of high-performance coatings and textiles. Industry compliance standards
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4. Advanced Organic Electronics Material FabricationProducers of organic semiconductors and optoelectronic components employ this molecule as a key monomer for developing high-mobility molecular crystals and charge-transfer complexes. The presence of trifluoromethyl and methylthio groups allows precise tuning of HOMO-LUMO energy levels to optimize device stability and efficiency. Manufacturers introduce this raw material during the precursor-polymerization or surface functionalization stage, ensuring integration into downstream photolithography and device assembly. Industry compliance standards
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5. Custom Fine Chemical Synthesis for Contract ManufacturingCustom synthesis providers and toll manufacturers source this specialty molecule for producing bespoke fine chemicals, such as specialty reagents and structure-activity probes. The unique electron-donating and withdrawing functionalities enable custom reactivity patterns in multi-step organic transformations. Process engineers control process sequencing to maximize yield and reduce batch variability, meeting project-specific documentation and audit requirements. Industry compliance standards
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