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HS Code |
268097 |
| Product Name | 2-(3-Bromophenyl)-1,3-Dioxolane |
| Cas Number | 65806-02-8 |
| Molecular Formula | C9H9BrO2 |
| Molecular Weight | 229.07 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 120-122°C at 1 mmHg |
| Density | 1.463 g/cm3 |
| Refractive Index | 1.545-1.548 |
| Flash Point | 102°C |
| Purity | Typically ≥97% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Smiles | C1COC(O1)C2=CC(=CC=C2)Br |
| Inchi | InChI=1S/C9H9BrO2/c10-8-3-1-2-7(6-8)9-4-11-5-12-9/h1-3,6,9H,4-5H2 |
As an accredited 2-(3-Bromophenyl)-1,3-Dioxolane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, sealed with a tamper-evident cap, labeled with chemical details and hazard symbols, contains 25 grams of 2-(3-Bromophenyl)-1,3-Dioxolane. |
| Shipping | 2-(3-Bromophenyl)-1,3-Dioxolane is shipped in tightly sealed containers under ambient conditions. It must be protected from moisture and direct sunlight. Classed as a laboratory chemical, it ships according to local and international regulations, typically requiring labeling for hazardous materials. Ensure compliance with all handling and transportation guidelines for safe delivery. |
| Storage | Store **2-(3-Bromophenyl)-1,3-dioxolane** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep away from incompatible substances such as strong oxidizing agents. Ensure the storage area is clearly labeled, and access is restricted to trained personnel. Follow all standard laboratory safety and chemical storage protocols. |
Applications of 2-(3-Bromophenyl)-1,3-Dioxolane in Industrial ManufacturingOur production of 2-(3-Bromophenyl)-1,3-dioxolane enables multiple advanced downstream manufacturing scenarios. The following sectors represent direct industrial applications supported by batch quantities, tailored QC protocols, and technical documentation prepared for global markets. 1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug (NSAID) Synthesis2-(3-Bromophenyl)-1,3-dioxolane serves as a critical intermediate in the synthesis of select NSAIDs, where its brominated aromatic functionality enables regioselective coupling with amine or acetic acid derivatives to produce novel analgesic actives. Synthesis teams introduce this raw material during key Friedel-Crafts or Suzuki coupling steps, under controlled temperature and inert atmosphere, to minimize side reactions and ensure purity required for regulated API manufacture. Industry compliance standards
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2. Agrochemical Synthesis – Herbicide Building BlockChemical processing plants utilize 2-(3-bromophenyl)-1,3-dioxolane as a brominated synthon for the preparation of aryl amine herbicide scaffolds. Downstream, it enters nucleophilic aromatic substitution and cyclization steps, enabling the precise introduction of functional groups critical for herbicidal selectivity. This pathway supports stricter purity requirements to reduce trace by-products affecting field efficacy and environmental compliance. Industry compliance standards
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3. Specialty Polymer Additive – Electronic Grade MaterialsOur 2-(3-bromophenyl)-1,3-dioxolane integrates as a monomeric additive in high-performance polymer backbones used for electronic encapsulants and dielectric materials. The brominated moiety imparts halogenated character for flame retardancy and alters dielectric constant profiles without introducing ionic impurities. Downstream compounding typically occurs in extruders or controlled reactors to maintain batch uniformity and minimize loss from volatilization. Industry compliance standards
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4. Fine Chemical Intermediate – Organic Light Emitting Diode (OLED) Material SynthesisManufacturers engaged in OLED display chemicals select 2-(3-bromophenyl)-1,3-dioxolane as a key halogenated precursor in the synthesis of arylamine and heterocycle-based emitters and host materials. Its molecular structure supports regioselective cross-coupling reactions, especially Suzuki and Buchwald-Hartwig protocols, and ensures the stringent photophysical property window required for high-brightness and color-purity devices. Industry compliance standards
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