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HS Code |
700465 |
| Productname | 2-Chloro-N-(2-Furylmethyl)Acetamide |
| Casnumber | 68787-98-2 |
| Molecularformula | C7H8ClNO2 |
| Molecularweight | 173.6 |
| Appearance | White to off-white solid |
| Meltingpoint | 76-78°C |
| Solubility | Soluble in organic solvents |
| Purity | Typically ≥98% |
| Storagetemperature | Store at 2-8°C |
| Smiles | ClCC(=O)NCC1=CC=CO1 |
| Inchikey | NZWYZUVOMIABLC-UHFFFAOYSA-N |
As an accredited 2-Chloro-N-(2-Furylmethyl)Acetamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a sealed, labeled amber glass bottle containing 25 grams, with hazard warnings and handling instructions clearly visible. |
| Shipping | Shipping for 2-Chloro-N-(2-Furylmethyl)acetamide is conducted in accordance with applicable chemical safety regulations. The compound is securely packaged in appropriate, labeled containers to prevent leakage or contamination. All shipments include safety documentation and are typically dispatched via certified carriers specializing in hazardous or specialty chemicals. Delivery timelines depend on destination and compliance checks. |
| Storage | 2-Chloro-N-(2-Furylmethyl)acetamide should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizing agents. Ensure proper labeling and access only to trained personnel. Always follow local regulations and chemical safety guidelines during storage and handling. |
Applications of 2-Chloro-N-(2-Furylmethyl)Acetamide in Industrial ManufacturingAs an established manufacturer of 2-Chloro-N-(2-Furylmethyl)Acetamide, we support specialized downstream industries that require this material for advanced synthesis and the development of distinct chemical-based products. Below we outline key industrial applications based on data from our long-standing partnerships with sector-leading producers. Each scenario focuses on core compliance, recipe inclusion, integration into the client’s facility, and the resulting finished goods. 1. Intermediate for Active Pharmaceutical Ingredient (API) SynthesisMajor pharmaceutical API producers rely on this compound as a key intermediate during the preparation of certain heterocyclic and furanyl-derived therapeutic molecules, especially antimicrobial or anti-inflammatory agents. The compound offers specific reactivity that allows regioselective substitution during multi-step organic synthesis, especially when introducing chloroacetyl side chains onto a furyl-based core. Process chemists adjust concentration according to conversion rate, impurity profiles, and target batch size, optimizing purity to meet regulatory filing requirements. Industry compliance standards
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2. Agrochemical Synthesis IntermediateManufacturers in the crop protection sector use this compound as a building block in the synthesis of selective fungicides and bactericides, specifically those leveraging furyl-acetamide scaffolds for targeted activity. Downstream formulators prefer this raw material due to its consistent reactivity and purity, which allow controlled chlorination and amidation steps in custom pesticide synthesis. Industry compliance standards
Typical usage ratio
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3. Chemical Synthesis Intermediate for Specialty PolymersProducers of niche polymers and specialty resins use this material as a crosslinking or functionalizing intermediate, taking advantage of its unique furylmethyl acetamide motif to impart hydrophilicity and chemical resistance to final polymer matrices. Production engineers tailor charge levels in formulation to achieve desired molecular weight and branching. Industry compliance standards
Typical usage ratio
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4. Fine Chemical Intermediate for Dye and Pigment ManufacturingAdvanced dye and pigment factories utilize this compound to synthesize high-value furan-based chromophores and intermediates for specialty colorants. Its electron-rich furan ring and reactive chloroacetamide group enable it to participate in ring-closure and acylation reactions that generate intensely colored molecules for dyes, plastics, and inks. Industry compliance standards
Typical usage ratio
Downstream process integration
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