Skip to Content
Merck
All Photos(2)

Documents

406554

Sigma-Aldrich

Diethyl malonimidate dihydrochloride

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C2H5OC(=NH)CH2C(=NH)OC2H5·2HCl
CAS Number:
10344-69-1
Molecular Weight:
231.12
MDL number:
MFCD00054633
UNSPSC Code:
12352100
PubChem Substance ID:
24865386
NACRES:
NA.22

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

Related Categories

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Chemical modification of urokinase with bis-imidoesters and properties of the intramolecularly cross-linked enzyme.
Yokoigawa K, et al.
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.
Debono N, et al.
Tetrahedron Letters, 45(10), 2235-2238 (2004)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service