Ethyl 4-nitrobenzoylacetate manufacturers
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| Ethyl 4-nitrobenzoylacetate Basic information |
| Ethyl 4-nitrobenzoylacetate Chemical Properties |
Melting point | 67-71 °C | Boiling point | 379.74°C (rough estimate) | density | 1.3350 (rough estimate) | refractive index | 1.5300 (estimate) | storage temp. | Sealed in dry,Room Temperature | pka | 8.70±0.25(Predicted) | form | powder to crystal | color | White to Light yellow to Light orange | BRN | 1124763 | InChI | InChI=1S/C11H11NO5/c1-2-17-11(14)7-10(13)8-3-5-9(6-4-8)12(15)16/h3-6H,2,7H2,1H3 | InChIKey | NGRXSVFCLHVGKU-UHFFFAOYSA-N | SMILES | C1(C=CC([N+]([O-])=O)=CC=1)C(=O)CC(=O)OCC | CAS DataBase Reference | 838-57-3(CAS DataBase Reference) | EPA Substance Registry System | Benzenepropanoic acid, 4-nitro-.beta.-oxo-, ethyl ester (838-57-3) |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 24/25-36/37-26 | WGK Germany | 2 | RTECS | AJ1073500 | TSCA | Yes | HazardClass | IRRITANT | HS Code | 29183000 |
| Ethyl 4-nitrobenzoylacetate Usage And Synthesis |
Chemical Properties | yellow fine crystalline powder | Uses | Reactant involved in:
- Synthesis of β-1,3-dicarbonyl aldehydes via oxidation
- Knoevenagel condensation using a lysine catalyst
- Cycloisomerization fo rthe synthesis of trisubstituted furans
- Fluorination by HF and iodosylbenzene
- Intramolecular Michael addition reactions for synthesis of benzylbutyrolactones
- Synthesis of diols via reduction of aromatic and aliphatic ketos esters
- Cross-coupling reactions for stereoselective synthesis of unsymmetrical 1,4-enediones
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| Ethyl 4-nitrobenzoylacetate Preparation Products And Raw materials |
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