HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 73106Erstellt: 27. Oktober 2026
Diethyl malonimidate
SKL193 · Diethyl malonimidate dihydrochloride · diethyl malonoimidate dihydrochloride · DIETHYLMALONDIIMIDATE DIHYDROCHLORIDE · DIETHYL MALONIMIDATE DIHYDROCHLORIDE, 97 % · MALONODIIMIDIC ACID DIETHYL ESTER HYDROCHLORIDE · propanediimidicacid,diethylester,dihydrochloride · Propanediimidic acid, 1,3-diethyl ester, hydrochloride (1:2)
https://huagongshe.com/de/chemical/73106
Identifikatoren & physikalische Daten
| CAS No. | 10344-69-1 |
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| Summenformel | C7H16Cl2N2O2 |
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| Durchschnittliche Molmasse | 231,12 g/mol |
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| Monoisotopische Masse | 230,05888311 g/mol |
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| SMILES | CCOC(=N)CC(=N)OCC.Cl.Cl |
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| InChIKey | TWUQXVGHXWRUBR-UHFFFAOYSA-N |
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| PubChem CID | 73106 |
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| DTXSID | DTXSID7065043 |
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Chemische & physikalische Eigenschaften
| Polarare Oberfläche (TPSA) | 66,2 |
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| H-Brücken-Donoren | 4 |
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| H-Brücken-Akzeptoren | 4 |
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| Frei drehbare Bindungen | 6 |
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| Schwere Atome | 13 |
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| Formalladung | 0 |
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| Komplexität | 129 |
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| Schmelzpunkt | 122 °C (dec.)(lit.) |
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| Lagerbedingungen | under inert gas (nitrogen or Argon) at 2-8°C |
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| InChI | 1S/C7H14N2O2.2ClH/c1-3-10-6(8)5-7(9)11-4-2/h8-9H,3-5H2,1-2H32*1H |
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| InChIKey | TWUQXVGHXWRUBR-UHFFFAOYSA-N |
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| SMILES | Cl.Cl.CCOC(=N)CC(=N)OCC |
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| EPA chemische Informationen | Propanediimidic acid, diethyl ester, dihydrochloride (10344-69-1) |
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Sicherheit & Vorschriften
| Wassergefährdungsklasse (WGK) | 3 |
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| TSCA-Inventar-Status | TSCA listed |
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| Zollcode | 2925199590 |
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| R-Sätze (R) | 36/37/38 |
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| Gefahrensymbole | Xi |
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| Sicherheitshinweise (S) | 26-36 |
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| Lagerklasse | 11 - Combustible Solids |
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| Gefahrenklasse | Eye Irrit. 2Skin Irrit. 2STOT SE 3 |
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Anwendungen & Verwendung
Verwenden
Reactant for:Preparation of rhenium cyanobis(oxazoline) oxo complexes as enantioselective reduction catalystsSynthesis of chiral bis(oxazoline)-copper complexes immobilized by donor-acceptor interactions on insoluble organic supports as reusable catalysts for asymmetric Diels-Alder cycloadditionPreparation of nonracemic bis(oxazoline)ruthenium p-cymene complexes and silica-supported analogs as catalysts for the enantioselective transfer hydrogenation of ketones to secondary alcohols
