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| | 5-Methylisoxazole-3-carboxylic acid Basic information |
| | 5-Methylisoxazole-3-carboxylic acid Chemical Properties |
| Melting point | 168 °C | | Boiling point | 312.5±22.0 °C(Predicted) | | density | 1.348±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Solid | | pka | 3.46±0.10(Predicted) | | color | Off-White to Pale Beige | | BRN | 114094 | | InChIKey | BNMPIJWVMVNSRD-UHFFFAOYSA-N | | CAS DataBase Reference | 3405-77-4(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-37/39 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29339900 |
| Provider | Language |
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ALFA
| English |
| | 5-Methylisoxazole-3-carboxylic acid Usage And Synthesis |
| Chemical Properties | Off-white solid | | Uses | 5-Methylisoxazole-3-carboxylic Acid is a metabolite of UTL-5b, a structural analog of the anti-arthritic drug, Leflunomide (L322750). | | Uses | Reactant for:
- Click/aza-Michael or Click/oligomeric alkyl carbodiimide esterification reactions
- Preparation of aminopyrazole amide derivatives as Raf kinase inhibitors in melanoma cells
- Preparation of trifluoromethoxyphenyl(thiazolyl)pyrroles and other heterocycle-bearing polyfunctionalized pyrroles via chain heterocyclization
| | Uses | Reactant for:• ;Click/aza-Michael or Click/oligomeric alkyl carbodiimide esterification reactions1• ;Preparation of aminopyrazole amide derivatives as Raf kinase inhibitors in melanoma cells2• ;Preparation of trifluoromethoxyphenyl(thiazolyl)pyrroles and other heterocycle-bearing polyfunctionalized pyrroles via chain heterocyclization3 |
| | 5-Methylisoxazole-3-carboxylic acid Preparation Products And Raw materials |
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