Thermo Scientific Chemicals

Ethyl nitroacetate, 97%, Thermo Scientific Chemicals

Catalog number: A14433.06
5 g, Each
Thermo Scientific Chemicals

Ethyl nitroacetate, 97%, Thermo Scientific Chemicals

Catalog number: A14433.06
5 g, Each
Quantity
Catalog number: A14433.06
also known as A14433-06
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Chemical Identifiers

CAS
626-35-7
IUPAC Name
ethyl 2-nitroacetate
Molecular Formula
C4H7NO4
InChI Key
FTKASJMIPSSXBP-UHFFFAOYSA-N
SMILES
CCOC(=O)C[N+]([O-])=O
Appearance (Color)
Clear colorless to pale yellow
Identification (FTIR)
Conforms
Assay (GC)
≥96.0%
Refractive Index
1.4220-1.4270 @ 20?C
Form
Liquid

Description

Ethyl nitroacetate has been used in the synthesis of γ-oxoacids via Michael addition reaction with α,β-unsaturated ketones, fuctionalization of C4-position on pyrimidine and C6-position on 2-deoxyguanosine to produce novel nucleosides, facile synthesis of α,α-diisobutylglycine, synthesis of DL-4,4-difluoroglutamic acid. It is also used as an intermediate in the preparation of unsubstituted amino acids.

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
Ethyl nitroacetate has been used in the synthesis of γ-oxoacids via Michael addition reaction with α,β-unsaturated ketones, fuctionalization of C4-position on pyrimidine and C6-position on 2′-deoxyguanosine to produce novel nucleosides, facile synthesis of α,α-diisobutylglycine, synthesis of DL-4,4-difluoroglutamic acid. It is also used as an intermediate in the preparation of unsubstituted amino acids.

Solubility
Slightly soluble in water. Soluble in chloroform and ethyl acetate.

Notes
Store away from bases and oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

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