missing translation for 'onlineSavingsMsg'
Learn More

Ethyl 4-nitrobenzoylacetate, 97%, Thermo Scientific Chemicals

Catalog Number 11458227
Click to view available options
Quantity:
10 g
50 g
250 g
This item is not returnable. View return policy
838-57-3
C11H11NO5
237.211
MFCD00007357
NGRXSVFCLHVGKU-UHFFFAOYSA-N
ethyl 4-nitrobenzoylacetate, ethyl 3-4-nitrophenyl-3-oxopropanoate, ethyl p-nitrobenzoyl acetate, ethyl 4-nitrobenzoyl acetate, p-nitrobenzoyl acetic acid ethyl ester, ethyl p-nitrobenzoylacetate, 4-nitrobenzoylacetic acid ethyl ester, ethyl 4-nitro-beta-oxobenzenepropanoate, 4-nitrobenzoyl acetic acid ethyl ester, benzenepropanoic acid, 4-nitro-beta-oxo-, ethyl ester
13281
ethyl 3-(4-nitrophenyl)-3-oxopropanoate
CCOC(=O)CC(=O)C1=CC=C(C=C1)[N+](=O)[O-]
This item is not returnable. View return policy
838-57-3
C11H11NO5
237.211
MFCD00007357
NGRXSVFCLHVGKU-UHFFFAOYSA-N
ethyl 4-nitrobenzoylacetate, ethyl 3-4-nitrophenyl-3-oxopropanoate, ethyl p-nitrobenzoyl acetate, ethyl 4-nitrobenzoyl acetate, p-nitrobenzoyl acetic acid ethyl ester, ethyl p-nitrobenzoylacetate, 4-nitrobenzoylacetic acid ethyl ester, ethyl 4-nitro-beta-oxobenzenepropanoate, 4-nitrobenzoyl acetic acid ethyl ester, benzenepropanoic acid, 4-nitro-beta-oxo-, ethyl ester
13281
ethyl 3-(4-nitrophenyl)-3-oxopropanoate
CCOC(=O)CC(=O)C1=CC=C(C=C1)[N+](=O)[O-]

It is employed as a reactant involved in synthesis of β-1,3-dicarbonyl aldehydes via oxidation, knoevenagel condensation using a lysine catalyst, and cycloisomerization for the synthesis of trisubstituted furans. It is also a reactant for the fluorination by HF and iodosylbenzene, intramolecular Michael addition reactions and synthesis of diols. Also applied in the synthesis of diols via reduction of aromatic and aliphatic ketos esters6 and cross-coupling reactions for stereo selective synthesis of unsymmetrical 1,4-enediones.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is employed as a reactant involved in synthesis of β-1,3-dicarbonyl aldehydes via oxidation, knoevenagel condensation using a lysine catalyst, and cycloisomerization for the synthesis of trisubstituted furans. It is also a reactant for the fluorination by HF and iodosylbenzene, intramolecular Michael addition reactions and synthesis of diols. Also applied in the synthesis of diols via reduction of aromatic and aliphatic ketos esters6 and cross-coupling reactions for stereo selective synthesis of unsymmetrical 1,4-enediones.

Notes
Store away from oxidizing agents. Keep the container tightly closed in a cool, dry place.
TRUSTED_SUSTAINABILITY
Melting Point 68°C to 73°C
Quantity 10 g
Beilstein 1124763
Formula Weight 237.21
Percent Purity 97%
Chemical Name or Material Ethyl 4-nitrobenzoylacetate

RUO – Research Use Only

missing translation for 'provideContentCorrection'

missing translation for 'productTitle'