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CAS No.: | 13472-00-9 |
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Name: | 2-(4-Aminophenyl)ethylamine |
Article Data: | 33 |
Molecular Structure: | |
Formula: | C8H12N2 |
Molecular Weight: | 136.197 |
Synonyms: | Phenethylamine,p-amino- (8CI);(p-Aminophenyl)ethylamine;2-(4-Aminophenyl)phenethylamine;2-(p-Aminophenyl)ethylamine;4-(2-Aminoethyl)benzenamine;4-(2-Aminoethyl)phenylamine;4-Amino-b-phenylethylamine;4-Aminobenzeneethanamine;4-Aminophenylethylamine;NSC 299558;NSC 9060;p-(2-Aminoethyl)aniline;p-Aminophenethylamine;b-(p-Aminophenyl)ethylamine; |
EINECS: | 236-739-2 |
Density: | 1.062 g/cm3 |
Melting Point: | 28-31 °C(lit.) |
Boiling Point: | 313.8 °C at 760 mmHg |
Flash Point: | 140.9 °C |
Solubility: | Insoluble in water. |
Appearance: | Light yellow solid or liquid |
Hazard Symbols: | C,Xi |
Risk Codes: | 34-20/21/22 |
Safety: | 26-36/37/39-45-27 |
Transport Information: | UN 3259 8/PG 2 |
PSA: | 52.04000 |
LogP: | 2.05150 |
p-aminophenylacetonitrile
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrazine hydrate; nickel In ethanol at 50 - 55℃; | 100% |
With hydrazine hydrate; nickel In ethanol at 50 - 55℃; Product distribution; Other aminoarylalkylnitriles. Object: selective reduction of the nitrile group.; | 100% |
With methanol; cobalt(II) chloride; diborane for 0.5h; Ambient temperature; | 97.7% |
2-(p-nitrophenyl)ethylamine
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogen In methanol at 20℃; under 760.051 Torr; | 100% |
With 5%-palladium/activated carbon; hydrogen In ethanol under 760.051 Torr; | 91% |
With hydrogenchloride; tin | |
With palladium on activated charcoal; hydrogen | |
With palladium on activated charcoal; hydrogen |
1-nitro-4-(2-nitroethyl)benzene
p-Aminophenethylamine
Conditions | Yield |
---|---|
With samarium diiodide; water; isopropylamine In tetrahydrofuran | 86% |
4-Nitrophenylacetonitrile
p-Aminophenethylamine
Conditions | Yield |
---|---|
With sodium tetrahydroborate; (-) In ethanol at 20℃; for 156h; | 77% |
With acetic anhydride; platinum Hydrogenation.Erhitzen des Reaktionsprodukts mit wss.Salzsaeure; | |
With ethanol; nickel Hydrogenation; |
1-azido-2-(4'-nitrophenyl)ethane
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride; indium In tetrahydrofuran at 20℃; for 7h; | 63% |
N-benzyloxycarbonyl-4-nitrophenethylamine
A
p-Aminophenethylamine
B
N-benzyloxycarbonyl-4-aminophenethylamine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal; ethylenediamine In tetrahydrofuran at 20℃; under 760 Torr; for 8h; Hydrogenation; | A n/a B 60% C n/a |
(p-aminophenyl)alanine
p-Aminophenethylamine
Conditions | Yield |
---|---|
With pyridoxal 5'-phosphate; aromatic L-amino acid decarboxylase In various solvent(s) at 30℃; for 48h; | 28% |
N-<2-(4-nitrophenyl)ethyl>phthalimide
p-Aminophenethylamine
Conditions | Yield |
---|---|
With sodium sulfide; water |
4-(2-(((methyl)carbonyl)amino)ethyl)aniline
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride |
N-<2-(4-nitrophenyl)ethyl>acetamide
p-Aminophenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride; tin; ethanol nachfolgendes Eindampfen; | |
Multi-step reaction with 2 steps 1: iron; aq.-ethanolic HCl 2: aqueous HCl View Scheme | |
With iron; acetic acid Eindampfen der alkalisch gemachten Loesung; |