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HS Code |
794131 |
| Cas Number | 3440-14-6 |
| Molecular Formula | C8H5ClN2 |
| Molecular Weight | 164.59 |
| Iupac Name | 2-chloroquinoxaline |
| Appearance | Pale yellow to light brown crystalline powder |
| Melting Point | 128-132°C |
| Boiling Point | 325.3°C at 760 mmHg |
| Density | 1.35 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 150.2°C |
| Smiles | C1=CC=C2C(=C1)N=CC=N2Cl |
| Refractive Index | 1.710 |
As an accredited 2-Chloroquinoxaline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 g, with tamper-evident seal; labeled with hazard symbols, chemical name, CAS number, and handling instructions. |
| Shipping | 2-Chloroquinoxaline is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. The package is clearly labeled with hazard information, and handled according to chemical safety regulations. Transportation complies with local and international guidelines for hazardous chemicals, using secure containers to prevent leakage or contamination during transit. |
| Storage | 2-Chloroquinoxaline should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep it protected from light and moisture. Clearly label the container and keep it away from direct sunlight. Always follow standard laboratory safety protocols and local regulations when storing this chemical. |
Applications of 2-Chloroquinoxaline in Industrial Manufacturing2-Chloroquinoxaline serves as a specialized intermediate in advanced chemical manufacturing. This compound plays a critical role for various industrial sectors, where its chemical structure enables targeted synthesis and complex end product development. Our facility supplies consistent quality and verified purity for downstream integration. 1. Pharmaceutical Intermediates for Kinase Inhibitor SynthesisPharmaceutical manufacturers utilize 2-Chloroquinoxaline as a core scaffold for the synthesis of heterocyclic kinase inhibitors, especially in targeted anti-cancer drug development. The specific halogenation at the quinoxaline ring allows precise nucleophilic substitution and further derivatization. Synthesis protocols demand tight control of the reaction environment to ensure selective modification and high final yield, with close adherence to registration batch reproducibility. Formulations often employ this intermediate in the assembly of complex quinoxaline-based molecules under GMP-compliant conditions, supporting the launch of new molecular entities. Industry compliance standards
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2. Agrochemical Synthesis: Fungicide and Herbicide IntermediatesMajor agrochemical plants employ 2-Chloroquinoxaline in the multi-step synthesis of systemic fungicides and selective herbicides. Its chlorinated aromatic structure enables the creation of bioactive molecules that impact plant-pathogen interactions. Downstream processes rely on clean substitution chemistry, often under inert gas, to ensure residue thresholds and product performance comply with current agricultural safety regulations. Production schedules coordinate with seasonal demand and field efficacy trials, with each batch validated for active content and residual solvents. Industry compliance standards
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3. Dye and Pigment Manufacturing: Heterocyclic Colorant PrecursorsIndustrial dye producers integrate 2-Chloroquinoxaline as a key heterocyclic building block for the synthesis of specialty pigments. Its unique aromatic structure enables the production of nitrogen-containing colorants with high lightfastness and solvent resistance. Typical synthesis involves electrophilic substitution and subsequent coupling steps to build extended chromophore systems. Quality control protocols require strict batch-traceability to ensure colorimetric consistency and compliance with restricted substance legislation. Industry compliance standards
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4. Material Science R&D: Advanced Polymer Additive DevelopmentResearch facilities and polymer manufacturers utilize 2-Chloroquinoxaline as a monomer unit in the fabrication of conductive and photoactive polymers. Its aromatic core and reactive chlorine substituent enable controlled copolymerization and functional material design. Pilot plant protocols stipulate precise dosing and reaction time to control molecular weight distribution and preserve functional group availability for subsequent crosslinking or performance tuning. The additive supports research into novel materials for electronics, sensors, and specialty coatings, with scale-up guided by progressive QC milestones. Industry compliance standards
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5. Specialty Fine Chemical Synthesis: Custom Heterocyclic Building BlocksCustom synthesis providers and fine chemical manufacturers select 2-Chloroquinoxaline as a versatile precursor for contract research and tailored molecular assembly. Its defined halogen position offers a starting point for elaborating multiple derivatives through cross-coupling and metal-catalyzed processes. Production batches require careful stoichiometric planning and purification to meet the diverse demands of R&D partners in the pharmaceutical, agrochemical, and electronics sectors. Full documentation and impurity profiles accompany each lot for seamless integration into proprietary projects. Industry compliance standards
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