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Details

Stereochemistry ACHIRAL
Molecular Formula C3H2N2
Molecular Weight 66.0614
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Malononitrile

SMILES

N#CCC#N

InChI

InChIKey=CUONGYYJJVDODC-UHFFFAOYSA-N
InChI=1S/C3H2N2/c4-2-1-3-5/h1H2

HIDE SMILES / InChI
Malononitrile is a weak cyanocarbon acid with exceptional reactivity. It is used extensively as a reactant or reaction intermediate since the methylene group and either one or both cyano groups can take part in condensation reactions to give a variety of additional products and heterocyclic compounds. This unique reactivity makes malononitrile an important chemical in research and in medical, industrial, and agricultural chemistry. In the late 1940's malononitrile was used experimentally in the treatment of schizophrenia and depression.

Approval Year

PubMed

PubMed

TitleDatePubMed
The effect of 5-alkyl modification on the biological activity of pyrrolo[2,3-d]pyrimidine containing classical and nonclassical antifolates as inhibitors of dihydrofolate reductase and as antitumor and/or antiopportunistic infection agents.
2008-08-14
Photochemical monoalkylation of propanedinitrile by electron-rich alkenes.
2008-07-03
Anti-inflammatory and analgesic activities of some newly synthesized pyridinedicarbonitrile and benzopyranopyridine derivatives.
2008-06
An efficient and facile synthesis of highly substituted 2,6-dicyanoanilines.
2008-05-02
Diammonium hydrogen phosphate as a versatile and efficient catalyst for the one-pot synthesis of pyrano[2,3-d]pyrimidinone derivatives in aqueous media.
2008-05
Reduced band gap dithieno[3,2-b:2',3'-d]pyrroles: new n-type organic materials via unexpected reactivity.
2008-04-17
One-step synthesis of polysubstituted benzene derivatives by multi-component cyclization of alpha-bromoacetate, malononitrile and aromatic aldehydes.
2008-03-28
temperature-dependent orientational dynamics of 1,n-dicyano n-alkanes.
2008-03-13
The condensation of salicylaldehydes and malononitrile revisited: synthesis of new dimeric chromene derivatives.
2008-03-07
Novel three-component synthesis and antiproliferative properties of diversely functionalized pyrrolines.
2008-02-15
Highly enantioselective Michael addition of malononitrile to alpha,beta-unsaturated ketones.
2008-01-21
Reaction of 1-tert-butyl-3,4-diphenyl-1,2,4-triazol-5-ylidenes with a malonic ester.
2008-01-07
The tert-amino effect in heterocyclic chemistry: synthesis of new fused pyrazolinoquinolizine and 1,4-oxazinopyrazoline derivatives.
2007-12-12
An atom efficient, solvent-free, green synthesis and antimycobacterial evaluation of 2-amino-6-methyl-4-aryl-8-[(E)-arylmethylidene]-5,6,7,8-tetrahydro-4H-pyrano[3,2-c]pyridine-3-carbonitriles.
2007-12-01
[(2-Phenylindol-3-yl)methylene]propanedinitriles inhibit the growth of breast cancer cells by cell cycle arrest in G(2)/M phase and apoptosis.
2007-12-01
SmCl3-catalyzed C-acylation of 1,3-dicarbonyl compounds and malononitrile.
2007-10-25
Synthesis of C2-symmetric bisamidines: a new type of chiral metal-free Lewis acid analogue interacting with carbonyl groups.
2007-07-20
Antiproliferative and apoptosis inducing properties of pyrano[3,2-c]pyridones accessible by a one-step multicomponent synthesis.
2007-07-15
Efficient method for the synthesis of polysubstituted benzenes by one-pot tandem reaction of vinyl malononitriles with nitroolefins.
2007-07-06
Theoretical study on the ground and excited states of dicyanocarbene (C3N2) and its isomers: a low-temperature matrix emission spectrum attributable to 3-cyano-2H-azirenylidene.
2007-06-07
One-step synthesis of heterocyclic privileged medicinal scaffolds by a multicomponent reaction of malononitrile with aldehydes and thiols.
2007-04-27
Radical reactions of [60]fullerene mediated by manganese(III) acetate dihydrate.
2007-04-25
An improved procedure for the three-component synthesis of highly substituted pyridines using ionic liquid.
2007-04-13
Novel synthesis of [1]-benzothiepino[5,4-b]pyridine-3-carbonitriles and their anti-inflammatory properties.
2007-03-15
2-Arylhydrazononitriles as building blocks in heterocyclic synthesis: A novel route to 2-substituted-1,2,3-triazoles and 1,2,3-triazolo[4,5-b]pyridines.
2007-03-13
An efficient synthesis of pyrazolo[3,4-b]quinolin-3-amine and benzo[b][1,8]naphthyridine derivatives.
2007-03-08
Molecular diodes and ultra-thin organic rectifying junctions: Au-S-CnH2n-Q3CNQ and TCNQ derivatives.
2007-02-28
Vibrational fingerprint of the structural tuning in push-pull organic chromophores with quinoid or proaromatic spacers.
2007-02-21
Hydrogen sulfide, nitric oxide and a molecular mass 66 u substance in the exhaled breath of chronic pancreatitis patients.
2007
Michael additions of methylene active compounds to chalcone in ionic liquids without any catalyst: the peculiar properties of ionic liquids.
2007
Investigation of the excited state structure of DCM via ultrafast electronic pump/vibrational probe.
2006-09-28
Thiourea-catalyzed asymmetric michael addition of activated methylene compounds to alpha,beta-unsaturated imides: dual activation of imide by intra- and intermolecular hydrogen bonding.
2006-07-26
Synthesis of water-soluble, ring-substituted squaraine dyes and their evaluation as fluorescent probes and labels.
2006-06-16
Synthesis and molluscicidal activity of some 1,3,4-triaryl-5-chloropyrazole, pyrano[2,3-c]pyrazole, pyrazolylphthalazine and pyrano[2,3-d]thiazole derivatives.
2006-06
Cloning, overexpression, and characterization of a thermoactive nitrilase from the hyperthermophilic archaeon Pyrococcus abyssi.
2006-06
One-step, three-component synthesis of pyridines and 1,4-dihydropyridines with manifold medicinal utility.
2006-03-02
[Reaction of pyridinium salts with active methylene compounds].
2006-02
[Reaction of pyridinium and quinolinium salts having the leaving group at the 2- or 4-position with active methylene compounds].
2006-02
Novel milrinone analogs of pyridine-3-carbonitrile derivatives as promising cardiotonic agents.
2005-12
Physical properties and intermolecular dynamics of an ionic liquid compared with its isoelectronic neutral binary solution.
2005-10-27
Elastic, quasielastic, and inelastic neutron-scattering studies on the charge-transfer hexamethylbenzene-tetracyanoquinodimethane complex.
2005-09-22
A novel synthesis and molluscicidal activity of some functionally substituted pyridine, pyrido[3,2-c]pyridazine, and pyrido[3,2-c]pyridazino[2',3'-a]quinazoline derivatives.
2005-07
Prevention of CS "tear gas" eye and skin effects and active decontamination with Diphoterine: preliminary studies in 5 French Gendarmes.
2005-07
Extensive quinoidal oligothiophenes with dicyanomethylene groups at terminal positions as highly amphoteric redox molecules.
2005-06-29
Solvent-free mechanochemical and one-pot reductive benzylizations of malononitrile and 4-methylaniline using Hantzsch 1,4-dihydropyridine as the reductant.
2005-05-07
Individual and combined toxicity of nitriles and aldehydes to Raphidocelis subcapitata.
2005-05
Post-Hartree-Fock studies on the structure of bis(ortho-substituted phenyl)methylenes.
2005-02-10
Knoevenagel reaction in water catalyzed by amine supported on silica gel.
2005
Functionalization of pyrimidine and purine nucleosides at C4 and C6: C-nucleophilic substitution of their C4- and C6-(1,2,4-triazol-1-yl) derivatives.
2005
Synthesis and some reactions of 3-chloro-2-(cyanomethylene)-1,2-dihydroquinoxalines.
2004-03-31
Patents

Sample Use Guides

In the late 1940's malononitrile was used experimentally in the treatment of schizophrenia and depression. ... Patients were given an intravenous infusion of 5% malononitrile for 10-69 min. The total dose during each treatment ranged from 1 to 6 mg/kg. Treatments were given 2-3 times/wk, with at least 1 day intervals. Ten to 20 min after the beginning of the infusion, all patients experienced tachycardia. In addition, redness, nausea, vomiting, headache, shivering, muscle spasms, & numbness were reported with varying frequency.
Route of Administration: Intravenous
Name Type Language
NSC-3769
Preferred Name English
Malononitrile
HSDB   MI  
Systematic Name English
Malonic dinitrile
Common Name English
Cyanoacetonitrile
Systematic Name English
Propanedinitrile
Systematic Name English
Malononitrile [HSDB]
Common Name English
Malononitrile [MI]
Common Name English
Dicyanomethane
Systematic Name English
Methylene cyanide
Systematic Name English
Code System Code Type Description
WIKIPEDIA
MALONONITRILE
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-703-2
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY
PUBCHEM
8010
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY
MERCK INDEX
m7045
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY Merck Index
NSC
3769
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID6021907
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY
CAS
109-77-3
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY
HSDB
2523
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY
CHEBI
33186
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY
FDA UNII
EBL1KKS93J
Created by admin on Mon Mar 31 18:57:21 GMT 2025 , Edited by admin on Mon Mar 31 18:57:21 GMT 2025
PRIMARY