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3-Aminocrotononitrile, (E)+(Z), 96%, Thermo Scientific Chemicals

Catalog Number 11337395
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Quantità:
100 g
500 g
Les retours ne sont pas autorisés pour ce produit. Consulta la politica di reso
1118-61-2
C4H6N2
82.11
MFCD00008071,MFCD00008071
DELJOESCKJGFML-DUXPYHPUSA-N
3-aminocrotononitrile, 2z-3-aminobut-2-enenitrile, 3-amino-2-butenenitrile, z-3-aminobut-2-enenitrile, beta-aminocrotononitrile, 3-amino-2-butenonitrile, 2-amino-1-propenecarbonitrile, 3-amino-crotononitrile, beta-amino-crotononitrile, 2z-3-amino-2-butenenitrile
5325263
(Z)-3-aminobut-2-enenitrile
C\C(N)=C/C#N
Les retours ne sont pas autorisés pour ce produit. Consulta la politica di reso
1118-61-2
C4H6N2
82.11
MFCD00008071,MFCD00008071
DELJOESCKJGFML-DUXPYHPUSA-N
3-aminocrotononitrile, 2z-3-aminobut-2-enenitrile, 3-amino-2-butenenitrile, z-3-aminobut-2-enenitrile, beta-aminocrotononitrile, 3-amino-2-butenonitrile, 2-amino-1-propenecarbonitrile, 3-amino-crotononitrile, beta-amino-crotononitrile, 2z-3-amino-2-butenenitrile
5325263
(Z)-3-aminobut-2-enenitrile
C\C(N)=C/C#N

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.3-Aminocrotononitrile, (E)+(Z), is used in reaction with aryldiazonium salts gave, instead of the expected triazene, 2-arylhydrazono-3-ketobutyronitrile by electrophilic attack at the ?-carbon and hydrolysis of the resulting imine. It is also used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. 3-Aminocrotononitrile was used as bisnucleophilic reagent which on cyclocondensation with hexafluoroacetone(ethoxycarbonylimine) forms bis(trifluoromethyl)pyrimidinones.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
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.3-Aminocrotononitrile, (E)+(Z), is used in reaction with aryldiazonium salts gave, instead of the expected triazene, 2-arylhydrazono-3-ketobutyronitrile by electrophilic attack at the ɑ-carbon and hydrolysis of the resulting imine. It is also used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. 3-Aminocrotononitrile was used as bisnucleophilic reagent which on cyclocondensation with hexafluoroacetone(ethoxycarbonylimine) forms bis(trifluoromethyl)pyrimidinones.

Solubility
Very soluble in water, soluble in ethanol.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents.
TRUSTED_SUSTAINABILITY
Materiale o nome chimico 3-Aminocrotononitrile
Nota nome (E)+(Z)
Punto di fusione ∼70°C to 75°C
Punti di ebollizione 120°C (4 mmHg)
Punto d'infiammabilità 154°C (309°F)
Quantità 500 g
Beilstein 1719815
Informazioni di solubilità Very soluble in water,soluble in ethanol.
Peso formulazione 82.11
Percent Purity 96%

RUO – Research Use Only

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