Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More

Ethyl 4-nitrobenzoylacetate, 97%

Catalog No. AAA1760309
Change view
Click to view available options
Quantity:
10 g
50 g
250 g
3 product options available for selection
Product selection table with 3 available options. Use arrow keys to navigate and Enter or Space to select.
Catalog No. Quantity
AAA1760309 10 g
AAA1760318 50 g
AAA1760330 250 g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 3 options available.
3 options
Catalog No. AAA1760309 Supplier Thermo Scientific Chemicals Supplier No. A1760309
Only null left
Add to Cart

CAS: 838-57-3 | C11H11NO5 | 237.211 g/mol

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

Chemical Identifiers

CAS 838-57-3
Molecular Formula C11H11NO5
Molecular Weight (g/mol) 237.211
MDL Number MFCD00007357
InChI Key NGRXSVFCLHVGKU-UHFFFAOYSA-N
Synonym 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
PubChem CID 13281
IUPAC Name ethyl 3-(4-nitrophenyl)-3-oxopropanoate
SMILES CCOC(=O)CC(=O)C1=CC=C(C=C1)[N+](=O)[O-]

Specifications

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
EINECSNumber 212-656-7
RTECSNumber AJ1073500
TSCA Yes
Recommended Storage Ambient temperatures

RUO – Research Use Only

Product Title
Select an issue

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.