10344-69-1

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10344-69-1 Structure

Identification	Back Directory
[Name] DIETHYL MALONIMIDATE DIHYDROCHLORIDE
[CAS] 10344-69-1
[Synonyms] SKL193 DIETHYL MALONIMIDATE DIHYDROCHLORIDE DIETHYLMALONDIIMIDATE DIHYDROCHLORIDE DIETHYL MALONIMIDATE DIHYDROCHLORIDE, 97 % MALONODIIMIDIC ACID DIETHYL ESTER HYDROCHLORIDE propanediimidicacid,diethylester,dihydrochloride Propanediimidic acid, 1,3-diethyl ester, hydrochloride (1:2)
[Molecular Formula] C7H16Cl2N2O2
[MDL Number] MFCD00054633
[MOL File] 10344-69-1.mol
[Molecular Weight] 231.12

Chemical Properties	Back Directory
[Melting point ] 122 °C (dec.)(lit.)
[storage temp. ] under inert gas (nitrogen or Argon) at 2-8°C
[EPA Substance Registry System] Propanediimidic acid, diethyl ester, dihydrochloride (10344-69-1)

Safety Data	Back Directory
[Symbol(GHS) ] GHS07
[Signal word ] Warning
[Hazard statements ] H315-H319-H335
[Precautionary statements ] P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ] Xi
[Risk Statements ] 36/37/38
[Safety Statements ] 26-36
[WGK Germany ] 3
[HS Code ] 2925199590

[Uses]

Reactant for:

Preparation of rhenium cyanobis(oxazoline) oxo complexes as enantioselective reduction catalysts
Synthesis of chiral bis(oxazoline)-copper complexes immobilized by donor-acceptor interactions on insoluble organic supports as reusable catalysts for asymmetric Diels-Alder cycloaddition
Preparation of nonracemic bis(oxazoline)ruthenium p-cymene complexes and silica-supported analogs as catalysts for the enantioselective transfer hydrogenation of ketones to secondary alcohols

Spectrum Detail	Back Directory
[Spectrum Detail] DIETHYL MALONIMIDATE DIHYDROCHLORIDE(10344-69-1)FT-IR

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