[A15468] CAS 105-53-3 | Diethyl malonate, 99% | Alfa
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Brand: Alfa Aesar
105-53-3 | C7H12O4 | diethyl malonate
Chemical Identifiers
CAS
105-53-3
Molecular Weight (g/mol)
160.17
Synonym
diethyl malonate
SMILES
CCOC(=O)CC(=O)OCC
InChI Key
IYXGSMUGOJNHAZ-UHFFFAOYSA-N
Molecular Formula
C7H12O4
IUPAC Name
1,3-diethyl propanedioate
Specifications
Assay (GC)
≥98.5%
Water Content (Karl Fischer Titration)
≤0.5%
Appearance (Color)
Clear colorless
Identification (FTIR)
Conforms
Form
Liquid
설명
Diethyl malonate is used in organic synthesis for the preparation of alpha-aryl malonates, mono-substituted and di-substituted acetic acid, barbiturates and artificial flavorings. It is also involved in the synthesis of pharmaceuticals like chloroquine, butazolidin and barbital. It acts as intermediate in the synthesis of vitamin B1, vitamin B6, non-steroidal anti-inflammatory agents agrochemicals and perfumes. In Knoevenagel condensation reaction, it reacts with benzaldehyde to get diethyl benzylidenemalonate.
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
Diethyl malonate is used in organic synthesis for the preparation of alpha-aryl malonates, mono-substituted and di-substituted acetic acid, barbiturates and artificial flavorings. It is also involved in the synthesis of pharmaceuticals like chloroquine, butazolidin and barbital. It acts as intermediate in the synthesis of vitamin B1, vitamin B6, non-steroidal anti-inflammatory agents agrochemicals and perfumes. In Knoevenagel condensation reaction, it reacts with benzaldehyde to get diethyl benzylidenemalonate.
Diethyl malonate is used in organic synthesis for the preparation of alpha-aryl malonates, mono-substituted and di-substituted acetic acid, barbiturates and artificial flavorings. It is also involved in the synthesis of pharmaceuticals like chloroquine, butazolidin and barbital. It acts as intermediate in the synthesis of vitamin B1, vitamin B6, non-steroidal anti-inflammatory agents agrochemicals and perfumes. In Knoevenagel condensation reaction, it reacts with benzaldehyde to get diethyl benzylidenemalonate.
Solubility
Miscible with ethyl alcohol, ether, chloroform and benzene. Slightly miscible with water.
Notes
Incompatible with acids, bases, oxidizing agents and reducing agents.
Other References:
Merck Index:14,3823Beilstein:774687
GHS Hazard and Precautionary Statements
Hazard Statements:H227
Precautionary Statements:P210-P280-P370+P378q-P501c
Risk & Safety
TSCA:YesRTECS Number:OO0700000
경고:RUO – Research Use Only
CAS105-53-3FORMULAC7H12O4EINECS203-305-9MDLMFCD00009195
| Pakage | 10000g, 2500g, 500g |
|---|---|
| brand | Alfa Aesar |
