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inquiryProduct Description Product Name 4-Nitrophenethylamine hydrochloride CAS No. 29968-78-3 Appearance Off-white to yellowish powder Assay ≥99% Capacity 100mt/year Min.pack
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inquiryProduct Name 4-Nitrophenethylamine hydrochloride Synonyms 4-NITROPHENYLETHYLAMINE HCL;4-NITROPHENYLETHYLAMINE HYDROCHLORIDE;4-NITROPHENETHYLAMINE HCL;4-NITROPHENETHYLAMINE HYDROCHLORIDE;2-(P-NITROPHENYL)ET
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inquiryMinimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
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inquiry4-Nitrophenethylamine hydrochloride CAS: 29968-78-3 Specification Product Name 4-Nitrophenethylamine hydrochloride CAS No. 29968-78-3 Appearance Off-white to yellowish powder Assay ≥99%
Cas:29968-78-3
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inquiryAppearance:white or light yellow crystalline powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:By
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Min.Order:100 Gram
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inquiryProduct Name: 4-Nitrophenethylamine hydrochloride Synonyms: 4-NitrophenylethylaMineydrochloride SynonyMs 2-(4-Nitrophenyl)ethylaMine hydrochloride;4- nitrobenzeneethylaMine hydrochloride;4-NitrophenylethylaMine HCl ( SM of Mirabegron );P-nitroph
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Min.Order:100 Gram
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inquiry1-azido-2-(4'-nitrophenyl)ethane
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
Stage #1: 1-azido-2-(4'-nitrophenyl)ethane With 1,3-diphenyl-disiloxane; triphenylphosphine at 20℃; for 24h; Staudinger Azide Reduction; Stage #2: With water Stage #3: With hydrogenchloride In 1,4-dioxane chemoselective reaction; | 99% |
Stage #1: 1-azido-2-(4'-nitrophenyl)ethane With triphenylphosphine at 110℃; for 20h; Staudinger Azide Reduction; Green chemistry; Stage #2: With hydrogenchloride In 1,4-dioxane; diethyl ether Reagent/catalyst; Solvent; Green chemistry; | 91% |
N-<2-(4-nitrophenyl)ethyl>acetamide
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water for 20h; pH=1; Reflux; Large scale; | 84.7% |
C11H14N2O3
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In methanol; water for 15h; pH=3; Solvent; pH-value; Reflux; Large scale; | 82.4% |
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In methanol; water for 5h; pH=1; Reflux; Large scale; | 81.2% |
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In propan-1-ol at 190℃; for 0.0833333h; Microwave irradiation; Green chemistry; | 74% |
2-phenylethylamine hydrochloride
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With nitric acid |
phenethylamine
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride; sulfuric acid; nitric acid 2) ether; Multistep reaction; |
4-nitro-3-phenyl-L-alanine
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: propan-1-ol / 20 - 190 °C / Green chemistry 2: hydrogenchloride / propan-1-ol / 0.08 h / 190 °C / Microwave irradiation; Green chemistry View Scheme |
2-(4-nitrophenyl)ethanol
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: triethylamine / dichloromethane / 5.5 h / -30 - 20 °C / Inert atmosphere 2.1: sodium azide / N,N-dimethyl-formamide / 20 h / 23 °C 3.1: triphenylphosphine / 20 h / 110 °C / Green chemistry 3.2: Green chemistry View Scheme |
<(p-Nitrophenyl)ethyl>-β-sulfonic ester
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: sodium azide / N,N-dimethyl-formamide / 20 h / 23 °C 2.1: triphenylphosphine / 20 h / 110 °C / Green chemistry 2.2: Green chemistry View Scheme |
2-(4-nitrophenyl)ethylamine monohydrochloride
trifluoroacetic anhydride
2,2,2-Trifluoro-N-(2-(4-nitrophenyl)ethyl)acetamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 1h; | 100% |
Stage #1: 2-(4-nitrophenyl)ethylamine monohydrochloride With triethylamine In dichloromethane at 0℃; Stage #2: trifluoroacetic anhydride In dichloromethane Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 20℃; for 2h; | 90% |
di-tert-butyl dicarbonate
2-(4-nitrophenyl)ethylamine monohydrochloride
(tert-butoxy)-N-[2-(4-nitrophenyl)-ethyl]-carboxamide
Conditions | Yield |
---|---|
With triethylamine In ethyl acetate at 20℃; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; | 99% |
With sodium hydrogencarbonate In 1,4-dioxane; water at 0 - 20℃; for 16.25h; | |
With hydrogenchloride; triethylamine In chloroform |
2-(4-nitrophenyl)ethylamine monohydrochloride
1-bromomethyl-4-nitro-benzene
Conditions | Yield |
---|---|
With sodium carbonate In water; N,N-dimethyl-formamide at 20 - 40℃; for 25h; Reagent/catalyst; | 99% |
2-(4-nitrophenyl)ethylamine monohydrochloride
benzaldehyde
Conditions | Yield |
---|---|
Stage #1: 2-(4-nitrophenyl)ethylamine monohydrochloride With sodium hydroxide In ethanol; water at 20℃; for 0.5h; Stage #2: benzaldehyde In ethanol at 80℃; for 16h; Inert atmosphere; Stage #3: With sodium tetrahydroborate at 20℃; for 1.5h; | 99% |
Stage #1: 2-(4-nitrophenyl)ethylamine monohydrochloride With sodium hydroxide In water; ethyl acetate at 25℃; for 1h; Stage #2: benzaldehyde In ethanol for 16h; Inert atmosphere; Reflux; Stage #3: With sodium tetrahydroborate In ethanol at 0 - 25℃; for 2h; | 97% |
tert-butyldicarbonate
2-(4-nitrophenyl)ethylamine monohydrochloride
(tert-butoxy)-N-[2-(4-nitrophenyl)-ethyl]-carboxamide
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In tetrahydrofuran at 0 - 20℃; | 96% |
bis-(p-nitrophenyl) carbonate
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran at 20℃; Inert atmosphere; | 96% |
With triethylamine In N,N-dimethyl-formamide at 58 - 62℃; for 2h; Reagent/catalyst; Solvent; | 86% |
2-(4-nitrophenyl)ethylamine monohydrochloride
acrylic acid methyl ester
Conditions | Yield |
---|---|
Stage #1: 2-(4-nitrophenyl)ethylamine monohydrochloride With sodium hydroxide In dichloromethane; water Stage #2: acrylic acid methyl ester In methanol for 16h; Reflux; | 96% |
pentafluorophenyl R-2,2-dimethyl-3-(N-(1,1-dimethylethoxycarbonyl)-L-phenylalanyl)tetrahydrothiazole-4-carboxylate
2-(4-nitrophenyl)ethylamine monohydrochloride
R-2,2-dimethyl-3-(N-(1,1-dimethylethoxycarbonyl)-L-phenylalanyl)-N-(2-(4-nitrophenyl)ethyl)tetrahydrothiazole-4-carboxamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 2h; | 95% |
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 23℃; for 16h; Inert atmosphere; | 95% |
2-(4-nitrophenyl)ethylamine monohydrochloride
L-(-)-N-(tert-butyloxycarbonyl)-2,2-dimethylthiazolidinecarboxylic acid pentafluorophenyl ester
R-2,2-dimethyl-3-(1,1-dimethylethoxycarbonyl)-N-(2-(4-nitrophenyl)ethyl)tetrahydrothiazole-4-carboxamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 2h; | 93% |
phosgene
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With 1,2-dichloro-benzene at 120℃; | 92% |
4-oxo-4-{{2-[(propylamino)carbonyl]phenyl}amino}butanoic acid
2-(4-nitrophenyl)ethylamine monohydrochloride
N1-[2-(4-nitrophenyl)ethyl]-N4-{2-[(propylamino)carbonyl]phenyl}butanediamide
Conditions | Yield |
---|---|
With 4-methyl-morpholine; O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate In dichloromethane; N,N-dimethyl-formamide at 20℃; for 2h; | 91% |
2-(4-nitrophenyl)ethylamine monohydrochloride
(R)-3-chloromandelic acid
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 20℃; for 2h; | 91% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 20℃; for 2h; | 91% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 20℃; for 2h; | 91% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 20℃; for 2h; | 91% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide In dichloromethane at 0 - 20℃; Inert atmosphere; | 90% |
With benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide In dichloromethane at 0 - 20℃; for 2h; Inert atmosphere; | 90% |
4-nitrophenyl N-(4-nitrobenzyl)carbamate
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran at 20℃; Inert atmosphere; | 90% |
2,4-dichloropyrido[2,3-d]pyrimidine
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With triethylamine In isopropyl alcohol at 21℃; for 5h; | 89% |
4-chloro-5,6-diphenylfuro[2,3-d]pyrimidine
2-(4-nitrophenyl)ethylamine monohydrochloride
N-[2-(4-nitrophenyl)ethyl]-5,6-diphenylfuro[2,3-d]pyrimidin-4-amine
Conditions | Yield |
---|---|
With triethylamine In ethanol at 80℃; for 8h; Inert atmosphere; | 88% |
(R)-Mandelic Acid
2-(4-nitrophenyl)ethylamine monohydrochloride
(2R)-2-hydroxy-N-[2-(4-nitrophenyl)ethyl]-2-phenylethanamide
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 0 - 20℃; | 86% |
Stage #1: (R)-Mandelic Acid With Trimethyl borate In acetonitrile at 28 - 58℃; for 1.5h; Stage #2: 2-(4-nitrophenyl)ethylamine monohydrochloride With N-ethyl-N,N-diisopropylamine In acetonitrile at 58℃; for 12h; Reflux; | 84.3% |
With Trimethyl borate; N-ethyl-N,N-diisopropylamine In acetonitrile for 8h; Reflux; | 82% |
N-(Benzyloxycarbonyloxy)succinimide
2-(4-nitrophenyl)ethylamine monohydrochloride
N-benzyloxycarbonyl-4-nitrophenethylamine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; for 17h; Acylation; | 82% |
2,3-dihydro-1,4-benzodioxin-6-carboxylic acid
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
Stage #1: 2,3-dihydro-1,4-benzodioxin-6-carboxylic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 1h; Stage #2: 2-(4-nitrophenyl)ethylamine monohydrochloride With dmap; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 24h; | 81% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl acetamide |
2-(4-nitrophenyl)ethylamine monohydrochloride
2,2,2-Trifluoro-N-(2-(4-nitrophenyl)ethyl)acetamide
Conditions | Yield |
---|---|
With triethylamine; trifluoroacetic anhydride In methanol; water | 80% |
With triethylamine; trifluoroacetic anhydride In methanol; water | 80% |
4,5,6,7-tetrafluoroisobenzofuran-1,3-dione
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
With acetic acid Reflux; | 80% |
(R)-4-(oxiran-2-yl)-2,8-bis(trifluoromethyl)quinoline
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
Stage #1: 2-(4-nitrophenyl)ethylamine monohydrochloride With sodium hydroxide Stage #2: (R)-4-(oxiran-2-yl)-2,8-bis(trifluoromethyl)quinoline In ethanol at 130℃; for 0.5h; Microwave irradiation; | 78% |
(S)-4-(oxiran-2-yl)-2,8-bis(trifluoromethyl)quinoline
2-(4-nitrophenyl)ethylamine monohydrochloride
Conditions | Yield |
---|---|
Stage #1: 2-(4-nitrophenyl)ethylamine monohydrochloride With sodium hydroxide Stage #2: (S)-4-(oxiran-2-yl)-2,8-bis(trifluoromethyl)quinoline In ethanol at 130℃; for 0.5h; Microwave irradiation; | 78% |
2-(4-nitrophenyl)ethylamine monohydrochloride
4-chloro-6-fluoro-quinazoline
Conditions | Yield |
---|---|
With triethylamine In isopropyl alcohol at 0 - 100℃; for 15h; | 78% |
2-(4-nitrophenyl)ethylamine monohydrochloride
1-phenyl-2-bromoethane
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 40℃; for 2h; | 77% |
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