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117641

Sigma-Aldrich

3-Aminocrotononitrile

96%

Synonym(s):

3-Amino-2-butenenitrile, 3-Iminobutyronitrile, Diacetonitrile

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About This Item

Linear Formula:
H2N(CH3)=CHCN
CAS Number:
Molecular Weight:
82.10
Beilstein:
1719815
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

solubility

95% ethanol: soluble 25 mg/mL, clear, colorless to yellow

storage temp.

2-8°C

SMILES string

C\C(N)=C/C#N

InChI

1S/C4H6N2/c1-4(6)2-3-5/h2H,6H2,1H3/b4-2+

InChI key

DELJOESCKJGFML-DUXPYHPUSA-N

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Application

3-Aminocrotononitrile was used as bisnucleophilic reagent which on cyclocondensation with hexafluoroacetone(ethoxycarbonylimine) forms bis(trifluoromethyl)pyrimidinones.

Biochem/physiol Actions

3-Aminocrotononitrile reacts with ferrocenyl-1,2-enones to form ferrocenyl pyridines. It undergoes diazotization coupling reaction with p-substituted anilines to give 2-arylhydrazone-3-ketimino-butyronitriles.

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Skin Sens. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

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Elena I Klimova et al.
Molecules (Basel, Switzerland), 17(9), 10079-10093 (2012-08-28)
The reactions of 2-cyano-3-ferrocenylacrylonitrile (1) with malononitrile (2) in a MeOH/H₂O or 2-PrOH/H₂O medium in the presence of Na₂CO₃ afforded 6-alkoxy-2-amino-4-ferrocenylpyridine-3,5-dicarbonitriles 3a,b (multi-component condensation) and 6-alkoxy-2-amino-4-ferrocenyl-3-ferrocenylmethyl-3,4-dihydropyridine-3,5-dicarbonitriles 4a,b (multi-component cyclodimerization). Analogous reactions of 1 with 2 in an MeOH/H₂O medium in
Synthesis of fluoro-containing pyrimidinones from hexafluoroacetone (ethoxycarbonylimine).
Sokolov VB and Aksinenko AY
Russian Chemical Bulletin, 54(6), 1518-1522 (2005)
Synthesis of disazo pyrazolo [1, 5-< i> a</i>] pyrimidines.
Karci F and Demircali A.
Dyes and Pigments, 74(2), 288-297 (2007)

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