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HS Code |
408965 |
| Chemical Name | 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid |
| Molecular Formula | C11H8ClNO3 |
| Molecular Weight | 237.64 g/mol |
| Cas Number | 130400-57-4 |
| Appearance | White to off-white solid |
| Melting Point | Approx. 170-174 °C |
| Solubility | Slightly soluble in water, soluble in DMSO and ethanol |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light |
| Smiles | CC1=CC(=NO1)C2=CC=CC=C2ClC(=O)O |
| Iupac Name | 3-(2-chlorophenyl)-5-methyl-1,2-oxazole-4-carboxylic acid |
As an accredited 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid 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, labeled "3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid", sealed, with hazard warnings. |
| Shipping | The chemical *3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid* is shipped in sealed, high-density polyethylene containers to prevent moisture and contamination. Packages are labeled according to regulatory requirements, with safety data sheets included. Temperature control and hazard classification are considered to ensure safe, compliant transport during domestic or international shipping. |
| Storage | Store **3-(2-Chlorophenyl)-5-methylisoxazole-4-carboxylic acid** in a tightly sealed container, protected from light and moisture. Keep at room temperature (15–25°C) in a well-ventilated, dry area away from incompatible substances such as strong acids, bases, and oxidizers. Ensure proper chemical labeling and secure storage to prevent unauthorized access or accidental release. |
Applications of 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid in Industrial ManufacturingAs a dedicated manufacturer of specialty intermediates, we supply 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carboxylic Acid to global chemical producers for incorporation into advanced downstream synthesis. Below, we detail specific industrial application scenarios with their unique requirements, processing methods, and end-use products, reflecting our insight into practical B2B use cases for this material. 1. Pharmaceutical Intermediate for Isoxazole-Based APIsDrug manufacturers utilize this compound primarily as a critical step in the synthesis of several isoxazole ring-containing active pharmaceutical ingredients, especially within the anti-inflammatory and CNS therapeutic segments. Its structure allows precise functionalization, supporting the formation of complex molecules through controlled reactions during multi-stage synthesis lines under strict quality assurance systems. Industry compliance standards
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2. Agrochemical Intermediate for Isoxazole Herbicides and FungicidesFormulators in agrochemical manufacturing employ this raw material as an isoxazole ring donor in synthesizing selective herbicide and fungicide actives. The chlorophenyl substitution provides enhanced target specificity and environmental stability, resulting in improved field persistence for end-use formulations targeting weed and fungal resistance in major crops. Industry compliance standards
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3. Fine Chemical Synthesis Building Block for Specialty Dyes and PigmentsSpecialty chemical producers use this carboxylic acid derivative as a building block for synthesizing advanced isoxazole chromophores, enabling the development of high-performance dyes and pigments with unique spectral and stability characteristics for plastic coloration, ink, and coating sectors. Its structural attributes allow precision in functional group introduction, facilitating the creation of tailor-made colorants with thermal and lightfast properties. Industry compliance standards
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4. Chemical Reagent for Isoxazole Scaffold Research and Analytical Reference MaterialsResearch laboratories and analytical standards producers procure this isoxazole derivative for use as a reference material or scaffold in the synthesis of structurally related molecules, particularly during the development of new bioactive compounds and in method validation QC protocols. The compound’s high purity and defined substitution pattern facilitate accurate calibration and extended structure-activity relationship (SAR) studies. Industry compliance standards
Typical usage ratio
Downstream process integration
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