Grundinformationen
- Standard-SMILES
CCOC=C(C(=O)OCC)C(=O)OCC- InChIKey
LTMHNWPUDSTBKD-UHFFFAOYSA-N- Summenformel
- C10H16O5
- Durchschnittliche Molmasse
- 216,23 g/mol
- Monoisotopische Masse
- 216,09977361
Namen und Bezeichner
- Bevorzugter Name
- Diethyl (ethoxymethylene)malonate
- IUPAC
- diethyl 2-(ethoxymethylidene)propanedioate
- Lokaler Name
- Diethylethoxymethylenmalonat
- Englischer Name
- Diethyl ethoxymethylenemalonate
- Summenformel
- C10H16O5
- Molmasse
- 216.23
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
87-13-8- PubChem CID
- 6871
- DTXSID
DTXSID5052591- UNII
- 6KF8220SZ8
- EC Number
- 201-725-7
- Nikkaji
- J61.661C
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,5
- Polarare Oberfläche (TPSA)
- 61,8 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 5
- Frei drehbare Bindungen
- 8
- Schwere Atome
- 15
- Formalladung
- 0
- Komplexität
- 224
Experimentelle und physikochemische Eigenschaften
Chemical Classes
Other Classes -> Esters, Other
Industrial compound
Ionization Efficiency
Positive
2.1
2.7
Agilent XCT
Electrospray ionization
formic acid (5.3nM)
Physikochemische Eigenschaften
- Schmelzpunkt
- -33 °C · -33°C
- Siedepunkt
- 279 · 279-283 °C(lit.)
- Dichte
- 1.08 g/mL · 1.080 g/mL at 20 °C(lit.)
- Dampfdruck
- 0.1 hPa · <0.1 hPa
- Brechungsindex
- 20 · n20/D 1.463
- Flammpunkt
- 311 °F · 311 °F
- storage temp.
- 30 °C · Store below +30°C.
- Löslichkeit
- Chloroform (Slightly), Ethyl Acetate (Slightly)
- Aggregatzustand
- Liquid
- Farbe
- Clear colorless to light yellow
- Wasserlöslichkeit
- insoluble
- BRN
- 880058 · 880058
- InChI
- 1S/C10H16O5/c1-4-13-7-8(9(11)14-5-2)10(12)15-6-3/h7H,4-6H2,1-3H3
- InChIKey
- LTMHNWPUDSTBKD-UHFFFAOYSA-N
- SMILES
- CCO\C=C(\C(=O)OCC)C(=O)OCC
- LogP
- 1.5 · 1.5-2.1 at pH7
- CAS Datenbank
- 87 · 87-13-8(CAS DataBase Reference)
- NIST chemische Informationen
- Propanedioic acid, (ethoxymethylene)-, diethyl ester(87-13-8)
- EPA chemische Informationen
- Propanedioic acid, (ethoxymethylene)-, diethyl ester (87-13-8)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H302 (99.1%): Harmful if swallowed [Warning Acute toxicity, oral]
P260, P261, P264, P264+P265, P270, P271, P272, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P333+P317, P337+P317, P362+P364, P363, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 111 reports by companies from 14 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Status: Active Update: 29-03-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/12518
Diethyl ethoxymethylenemalonate: Does not have an individual approval but may be used under an appropriate group standard
Hazards Summary
A moderate skin irritant; Causes somnolence and gastrointestinal changes in oral lethal-dose studies of rats; [RTECS] An irritant; May cause skin and respiratory sensitization; Harmful by ingestion; [Alfa Aesar MSDS] Search for (87-13-8[EC/RN Number]) AND (allergic OR dermatitis OR asthma OR sensitizer OR sensitization): no results; [PubMed]
Peroxide Forming Chemical
Diethyl ethoxymethylenemalonate
D: Other compounds that may form peroxides
Kelly
Toxikologische Informationen
Sicherheitsdaten
- wgk
- 1
- tsca
- TSCA listed
- hs_code
- 29189090
- RTECS-Nr.
- OO1100000
- risk_code
- 22-36/37/38-42/43
- Toxizität
- LD50 orally in Rabbit: 925 mg/kg LD50 dermal Rat > 2000 mg/kg
- hazard_code
- Xn
- safety_code
- 26-36/37/39-27-24/25
- Speicherklasse
- 10 - Combustible liquids
- Hazard Classifications
- Acute Tox. 4 OralAquatic Acute 1Aquatic Chronic 2Eye Irrit. 2Skin Irrit. 2Skin Sens. 1A
- Selbstentzündungstemperatur
- 215 °C
Chemie und Industrie
Verwendung und Herstellung
Anwendungen
VerwendenDiethyl ethoxymethylenemalonate is used for synthesis of pyrido[3,2-e]pyrimido[1,2-c]pyrimidines. Initially, it was used to monitor lysine decarboxylase activity. It is useful in the determination of amino acids by precolumn derivatization by using reversed-phase high-performance liquid chromatography (HPLC). It plays an important role in the Gould-Jacobs reaction to prepare quinolines. For example, anile reacts with this reagent to give 4-hydroxyquinoline. It acts as an intermediate in the production of flumequine, which is a fluoroquinolone antibiotic.
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