| Weight | 66.063 g/mol |
|---|---|
| Formula | C3H2N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
MALONONITRILE (109-77-3)
malonitrile · dicyanmethane · malonodinitrile
Score:
#494 in Physics
,
#1445 in Chemistry
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- Core-Expanded Naphthalene Diimides Fused with 2-(1,3-Dithiol-2-Ylidene)Malonitrile Groups for High-Performance, Ambient-Stable, Solution-Processed n-Channel Organic Thin Film Transistors (Journal of the American Chemical Society, 2010)
- In vitro detection of (S)-naproxen and ibuprofen binding to plaques in the Alzheimers brain using the positron emission tomography molecular imaging probe 2-(1-{6-[(2-[18F]fluoroethyl)(methyl)amino]-2-naphthyl}ethylidene)malononitrile (Neuroscience, 2003)
- Coumarin-malonitrile conjugate as a fluorescence turn-on probe for biothiols and its cellular expression. (Chemical Communications, 2011)
- One-Step Synthesis of Heterocyclic Privileged Medicinal Scaffolds by a Multicomponent Reaction of Malononitrile with Aldehydes and Thiols. (Journal of Organic Chemistry, 2007)
- Chemistry of malononitrile (Chemical Reviews, 1969)
- New Applications of Malononitrile in Organic Chemistry - Part II (Synthesis, 1978)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H319: Causes serious eye irritation
Warning Serious eye damage/eye irritation - Category 2A - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - malonitrile
- dicyanmethane
- malonodinitrile
-
SMILESC(C#N)C#N
-
InChIKeyCUONGYYJJVDODC-UHFFFAOYSA-N
- Pubchem - MALONONITRILE
- Wikipedia - Malononitrile
Malononitrile, also propanedinitrile or malonodinitrile, is a nitrile with the formula CH2(CN)2. Malononitrile is relatively acidic, with a pKa of 11 in water. This allows it to be used in the Knoevenagel condensation, for example in the preparation of CS gas: In related chemistry, malononitrile is a suitable starting material for the Gewald reaction, where the nitrile condenses with a ketone or aldehyde in the presence of elemental sulfur and a base to produce a 2-aminothiophene.
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MALONONITRILE
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