Diethyl ethoxymethylenemalonate

CAS Number: 87-13-8
Chemical Formula: C10H16O5
Synonyms: 1,1-DICARBETHOXY-2-ETHOXYETHYLENE, 2,2-DICARBETHOXYVINYL ETHYL ETHER, AKOS BBS-00004230
Appearance: Colorless Liquid
MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)

Products Description

Diethyl ethoxymethylenemaleic-anhydride.html">malonate shows moderate toxicity if swallowed and can irritate the skin. It is a combustible liquid. When exposed to high temperatures for decomposition, it releases pungent and irritating fumes.Diethyl ethoxymethylenemalonate

Chemical Properties

ItemValue
Melting point-33°C
Boiling point279-283 °C(lit.)
density1.080 g/mL at 20 °C(lit.)
vapor pressure<0.1 hPa
refractive indexn20/D 1.463
Fp311 °F
storage temp.Store below +30°C
solubilityChloroform (Slightly), Ethyl Acetate (Slightly)
formLiquid
colorClear colorless to light yellow
Water Solubilityinsoluble
BRN880058
InChI1S/C10H16O5/c1-4-13-7-8(9(11)14-5-2)10(12)15-6-3/h7H,4-6H2,1-3H3
InChIKeyLTMHNWPUDSTBKD-UHFFFAOYSA-N
SMILESCCO\C=C(\C(=O)OCC)C(=O)OCC
LogP1.5-2.1 at pH7
CAS DataBase Reference87-13-8(CAS DataBase Reference)
NIST Chemistry ReferencePropanedioic acid, (ethoxymethylene)-, diethyl ester(87-13-8)
EPA Substance Registry SystemPropanedioic acid, (ethoxymethylene)-, diethyl ester (87-13-8)

Safety Information

ItemValue
Hazard CodesXn
Risk Statements22-36/37/38-42/43
Safety Statements26-36/37/39-27-24/25
WGK Germany1
RTECSOO1100000
Autoignition Temperature215 °C
TSCATSCA listed
HS Code29189090
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Oral; Aquatic Acute 1; Aquatic Chronic 2; Eye Irrit. 2; Skin Irrit. 2; Skin Sens. 1A
ToxicityLD50 orally in Rabbit: 925 mg/kg; LD50 dermal Rat > 2000 mg/kg

Product Application

Diethyl ethoxymethylenemalonate is applied in the synthesis of pyrido[3,2-e]pyrimido[1,2-c]pyrimidines. It was first used to detect lysine decarboxylase activity. It supports amino acid analysis via precolumn derivatization in reversed‑phase HPLC. It is a key reagent in the Gould Jacobs reaction for quinoline synthesis, such as forming 4-8-hydroxyquinoline.html">hydroxyquinoline from aniline. It also serves as an intermediate for manufacturing flumequine, a fluoroquinolone antibiotic.

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