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HS Code |
768316 |
| Name | 4-Chloro-3-Fluoroiodobenzene |
| Molecularformula | C6H3ClFI |
| Molecularweight | 255.45 g/mol |
| Casnumber | 112307-02-9 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 221-223 °C |
| Density | 1.89 g/cm³ |
| Purity | Typically ≥97% |
| Smiles | C1=CC(=C(C=C1I)F)Cl |
| Inchi | InChI=1S/C6H3ClFI/c7-4-1-2-5(8)6(9)3-4/h1-3H |
| Solubility | Insoluble in water; soluble in organic solvents |
| Refractiveindex | 1.610 (at 20 °C) |
| Storageconditions | Store in a cool, dry place |
As an accredited 4-Chloro-3-Fluoroiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Chloro-3-Fluoroiodobenzene is packaged in a 25g amber glass bottle with a tamper-evident, screw cap for safe storage. |
| Shipping | **Shipping Description for 4-Chloro-3-Fluoroiodobenzene:** This compound should be shipped in a tightly sealed container, protected from light and moisture. Handle as a hazardous chemical; ensure compliance with local, national, and international transport regulations (UN number, if applicable). Ship in secondary containment with appropriate labeling and documentation. Avoid extreme temperatures and physical shocks. |
| Storage | 4-Chloro-3-fluoroiodobenzene should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of heat, ignition, and direct sunlight. Store separately from incompatible substances such as strong oxidizers. Label the container clearly and ensure appropriate chemical safety measures are followed to prevent accidental exposure, inhalation, or environmental release. |
Applications of 4-Chloro-3-Fluoroiodobenzene in Industrial ManufacturingAs a direct chemical manufacturer, we supply 4-Chloro-3-Fluoroiodobenzene for value-driven downstream segments. Below are verified industrial applications, each structured by sector, compliance, process integration, and finished product class. These details reflect current manufacturer usage, regulatory context, and production methods. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers apply this compound as a halogenated aromatic intermediate during small-molecule drug development. Its halogen pattern supports nucleophilic substitution, Suzuki-Miyaura, and Buchwald–Hartwig coupling reactions, enabling precise molecule construction for target drug candidates. Use typically occurs during early- to mid-stage synthesis, with stringent controls on solvent residues and elemental impurities to support downstream purification and API isolation processes. Industry compliance standards
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2. Agrochemical Active Ingredient ProductionAgrochemical manufacturers utilize this raw material to construct aromatic scaffolds in herbicide and insecticide synthesis, especially where selective halogenation impacts biological activity. The compound is frequently involved in constructing intermediates for pyridine and phenoxy herbicides, where controlled incorporation of chloro and fluoro groups is essential for binding affinity and environmental persistence. Industry compliance standards
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3. Advanced Material & Liquid Crystal Monomer ProductionSpecialty chemical producers source this intermediate for synthesizing liquid crystal monomers and advanced display materials. The compound’s unique halogen distribution introduces controlled dipole moments and thermal stability for high-performance nematic and smectic phases. Its use ensures consistent birefringence and voltage thresholds required by the electronics industry in OLED and flat panel display devices. Industry compliance standards
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4. Fine Chemical and Dye Intermediate ManufacturingColorant and pigment manufacturers select this compound for synthesizing fluorinated or halogenated dye intermediates, contributing to chromophore modification and bathochromic shift control. Its structure enables late-stage functionalization for dye stability in textile, printing, and inkjet applications. Its use supports consistent batch-to-batch absorbance properties and lightfastness essential in industrial dye lines. Industry compliance standards
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5. Custom Synthesis for Active Ingredient DiscoveryCustom synthesis labs and discovery chemistry groups employ this material in the design of novel aromatic scaffolds for lead generation projects. Its reactive iodo substituent and electron-withdrawing behavior support the formation of rare substitution patterns through metal-catalyzed cross-coupling, feeding QSAR-directed compound libraries. Stringent traceability and impurity controls are required to document route reproducibility. Industry compliance standards
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