3-Aminocrotononitrile

3-Aminocrotononitrile Basic information
Product Name:3-Aminocrotononitrile
Synonyms:(2E)-3-Amino-2-butenenitrile;3-amino-2-butenenitril;DIONIL;3-Amino-3-methylacrylonitrile;3-AMinocrotononitrile, Mixture of cis and trans, 96% 100GR;3-AMinocrotononitrile, Mixture of cis and trans, 96% 500GR;3-Amino-2-butenonitrile Diacetonitrile;3-AMinocrotononitrile cis+trans
CAS:1118-61-2
MF:C4H6N2
MW:82.1
EINECS:214-266-2
Product Categories:Intermediates of Dyes and Pigments
Mol File:1118-61-2.mol
3-Aminocrotononitrile Structure
3-Aminocrotononitrile Chemical Properties
Melting point 79-81°C
Boiling point 120°C 4mm
density 0.952
refractive index 1.4449 (estimate)
Fp 154°C
storage temp. 2-8°C
solubility 95% ethanol: soluble25mg/mL, clear, colorless to yellow
pka3.88±0.70(Predicted)
form Flakes
color Yellow
Water Solubility Very soluble in water, soluble in ethanol.
BRN 1719815
LogP0.005 (est)
CAS DataBase Reference1118-61-2(CAS DataBase Reference)
NIST Chemistry Reference2-Butenenitrile, 3-amino-(1118-61-2)
EPA Substance Registry System2-Butenenitrile, 3-amino- (1118-61-2)
Safety Information
Hazard Codes Xn,T
Risk Statements 22-20/21/22-43-24/25
Safety Statements 22-24/25-29-36/37-45
RIDADR UN 3439 6.1/PG 3
WGK Germany 3
TSCA Yes
PackingGroup III
HS Code 29269090
MSDS Information
ProviderLanguage
3-Amino-2-butenenitrile English
SigmaAldrich English
ACROS English
ALFA English
3-Aminocrotononitrile Usage And Synthesis
Chemical PropertiesYellowish flakes
Uses3-Aminocrotononitrile is used as intermediate for the syntheses of heterocycles (e.g. pyridines and pyrimidines) and for the production of polyurethane). It is used in the pharmaceutical (e.g. production of sulfsomizole) and dyestuff industries. Product Data Sheet
Uses3-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.
Biochem/physiol Actions3-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.
2-((3,5-BIS(TRIFLUOROMETHYL)PHENYL)AMINO)ETHENE-1,1,2-TRICARBONITRILE Polybutene 2-AMINO-1-(1-AZA-2-(2-THIENYL)VINYL)ETHENE-1,2-DICARBONITRILE BUTTPARK 116\40-76 2-HYDRAZINO-1-METHYL-6-OXO-4-(2-THIENYL)-1,6-DIHYDROPYRIMIDINE-5-CARBONITRILE 2-((3-(TRIFLUOROMETHYL)PHENYL)AMINO)ETHENE-1,1,2-TRICARBONITRILE EC 2.6.1.2 ALTRENOGEST Crotononitrile (pract) 2-[(4-CHLOROBENZYLIDENE)AMINO]-3-([(2,4-DICHLORO-1,3-THIAZOL-5-YL)METHYL]AMINO)BUT-2-ENEDINITRILE BUTTPARK 116\40-69 3-AMINOCROTONONITRILE, (DIACETONITRILE; 3-IMINOBUTYRONITRILE),3-AMINOCROTONONITRILE, (DIACETONITRILE; 3-IMINOBUTYRONITRILE) 2-AMINO-1-(1-AZA-2-(2-PYRIDYL)VINYL)ETHENE-1,2-DICARBONITRILE TYRPHOSTIN A51 2-AMINO-3-([(2,4-DICHLORO-1,3-THIAZOL-5-YL)METHYL]AMINO)BUT-2-ENEDINITRILE AMINO ACIDS 2-AMINO-1-PROPENE-1,1,3-TRICARBONITRILE 2-((3,5-DICHLOROPHENYL)AMINO)ETHENE-1,1,2-TRICARBONITRILE

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.