| Identification | Back Directory | [Name]
ETHYL ISOXAZOLE-3-CARBOXYLATE | [CAS]
3209-70-9 | [Synonyms]
AKOS PAO-1389
4-CHLOROISOINDOLINE HCL
3-Ethoxycarbonylisoxazole
Ethyl 3-isoxazolecarboxylate
Ethyl isoxazol-3-carboxylate
Ethyl isoxazole-3-carboxy...
ETHYL ISOXAZOLE-3-CARBOXYLATE
Methyl isoxazole-3-carboxylate
4-ethyl-3-isoxazolecarboxylate
ethyl 1,2-oxazole-3-carboxylate
Ethyl 5-isoxazole-3-carboxylate
4-ethyl-1,2-oxazole-3-carboxylate
3-Isoxazolecarboxylic acid ethyl ester
isoxazole-3-carboxylic acid ethyl ester | [Molecular Formula]
C6H7NO3 | [MDL Number]
MFCD08234628 | [MOL File]
3209-70-9.mol | [Molecular Weight]
141.12 |
| Chemical Properties | Back Directory | [Boiling point ]
219℃ | [density ]
1.177 | [Fp ]
87℃ | [storage temp. ]
Sealed in dry,Store in freezer, under -20°C | [pka]
-5.43±0.50(Predicted) | [InChI]
InChI=1S/C6H7NO3/c1-2-9-6(8)5-3-4-10-7-5/h3-4H,2H2,1H3 | [InChIKey]
RKXWKTOBQOSONL-UHFFFAOYSA-N | [SMILES]
O1C=CC(C(OCC)=O)=N1 |
| Hazard Information | Back Directory | [Uses]
Ethyl Isoxazol-3-carboxylate has been used as a reactant in the preparation of demethyl 2-amino-3-(3-carboxy-5-methyl-4-isoxazolyl)propionic acid (ACPA) which shows activity at metabotropic receptors and is a weak antagonist at the mGlu2 receptor subtype. | [Synthesis Reference(s)]
Canadian Journal of Chemistry, 48, p. 467, 1970 DOI: 10.1139/v70-075 |
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