Recommended Products
impurities
<5% ammonium chloride
mp
122 °C (dec.) (lit.)
SMILES string
Cl.Cl.CCOC(=N)CC(=N)OCC
InChI
1S/C7H14N2O2.2ClH/c1-3-10-6(8)5-7(9)11-4-2;;/h8-9H,3-5H2,1-2H3;2*1H
InChI key
TWUQXVGHXWRUBR-UHFFFAOYSA-N
Application
Diethyl malonimidate dihydrochloride may be used in the preparation of chiral bis(oxazoline) ligands. It may be used in the preparation of intramolecularly cross-linked urokinase.
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Chemical modification of urokinase with bis-imidoesters and properties of the intramolecularly cross-linked enzyme.
Agricultural and Biological Chemistry, 53(7), 1837-1842 (1989)
New chiral bis (oxazoline) Rh (I)-, Ir (I)-and Ru (II)-complexes for asymmetric transfer hydrogenations of ketones.
Tetrahedron Letters, 45(10), 2235-2238 (2004)
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