Weight | 108.104 g/mol |
---|---|
Formula | C4H4N4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
DIAMINOMALEONITRILE (18514-52-8, 1187-42-4)
diaminomaleonitrile, (Z)-isomer
Score:
#1600 in Physics
,
#4887 in Chemistry
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- Hydrogen cyanide chemistry. VIII. New chemistry of diaminomaleonitrile. Heterocyclic synthesis (Journal of Organic Chemistry, 1974)
- Coordination Compounds of Schiff-Base Ligands Derived from Diaminomaleonitrile (DMN): Mononuclear, Dinuclear, and Macrocyclic Derivatives. (Inorganic Chemistry, 1996)
- New syntheses and solid state fluorescence of azomethine dyes derived from diaminomaleonitrile and 2,5-diamino-3,6-dicyanopyrazine (Dyes and Pigments, 2000)
- A diaminomaleonitrile based selective colorimetric chemosensor for copper(II) and fluoride ions (New Journal of Chemistry, 2015)
- Defect-sensitive crystals based on diaminomaleonitrile-functionalized Schiff base with aggregation-enhanced emission (Journal of Materials Chemistry C, 2013)
- The molecular and crystal structure of hydrogen cyanide tetramer (diaminomaleonitrile) (Acta Crystallographica, 1961)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - diaminomaleonitrile, (Z)-isomer
-
SMILESC(#N)C(=C(C#N)N)N
-
InChIKeyDPZSNGJNFHWQDC-UHFFFAOYSA-N
- Pubchem - DIAMINOMALEONITRILE
- Wikipedia - Diaminomaleonitrile
Diaminomaleonitrile (DAMN) is an organic compound composed of two amino groups and two nitrile groups bonded to a central alkene unit. The systematic name reflects its relationship to maleic acid. The chemical can be formed by polymerization of hydrogen cyanide and can be used as the starting point for the synthesis of several classes of heterocyclic compounds.
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