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inquiryBeluga chemical professional supply 4-Amino-3-phenylbutyric acid CAS:1078-21-3 Phenibut Why choose Beluga chemical 1. Beluga Chemical has a professional RESEARCH and development team and strong technical force to ensure technical support and res
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Min.Order:1 Kilogram
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inquiryHebei Mojin Biological Technology Co., Ltd. is specialize in the production of chemical raw materials and reagents,located in Shijiazhuang, Hebei Province. In recent decades, under the efforts of all staff, in Shandong, Henan, Guangdong and many o
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Min.Order:1 Kilogram
Negotiable
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inquiryItems Standard Result Appearance White crystalline powder White crystalline powder Identification
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inquiryIntroduction Also known as “4-Amino-3-Phenylbutyric Acid,” Phenibut is a non-prescription pharmaceutical that is actually a GABA molecule with the addition of a phenyl group. Russian researchers discovered that by chan
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Min.Order:1 Kilogram
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4-nitro-3-phenylbutanoic acid
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol at 60℃; under 45004.5 Torr; | 98% |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride In water at 130℃; for 24h; Sealed tube; | 95% |
2-oxo-4-phenyl-3-ethoxycarbonylpyrrolidine
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
With hydrogenchloride Heating; |
3-cyano-3-phenyl propionic acid
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In acetic acid under 15200 Torr; |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide; sodium hypobromide |
hydrogenchloride
3-phenyl-glutaric acid dihydrazide
isopentyl nitrite
B
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
at 25℃; Kochen mit Bromwasserstoffsaeure; |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate; sodium hypochlorite; potassium bromide / water; dichloromethane / 0.21 h / 0 °C 2.1: potassium tert-butylate / toluene; methanol / 0.17 h / 20 °C / 4500.45 Torr / Inert atmosphere 2.2: 0.11 h / 25 °C / 4500.45 Torr / Inert atmosphere 3.1: tetrabutyl ammonium fluoride / toluene; tetrahydrofuran / 1 h / 50 °C / 6000.6 Torr 4.1: lithium hydroxide; water / toluene / 1 h / 50 °C / 3750.38 Torr 5.1: hydrogen; palladium 10% on activated carbon / methanol / 60 °C / 45004.5 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: potassium tert-butylate / toluene; methanol / 0.17 h / 20 °C / 4500.45 Torr / Inert atmosphere 1.2: 0.11 h / 25 °C / 4500.45 Torr / Inert atmosphere 2.1: tetrabutyl ammonium fluoride / toluene; tetrahydrofuran / 1 h / 50 °C / 6000.6 Torr 3.1: lithium hydroxide; water / toluene / 1 h / 50 °C / 3750.38 Torr 4.1: hydrogen; palladium 10% on activated carbon / methanol / 60 °C / 45004.5 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: tetrabutyl ammonium fluoride / toluene; tetrahydrofuran / 1 h / 50 °C / 6000.6 Torr 2: lithium hydroxide; water / toluene / 1 h / 50 °C / 3750.38 Torr 3: hydrogen; palladium 10% on activated carbon / methanol / 60 °C / 45004.5 Torr View Scheme |
4-nitro-3-phenylbutanoic acid methyl ester
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: lithium hydroxide; water / toluene / 1 h / 50 °C / 3750.38 Torr 2: hydrogen; palladium 10% on activated carbon / methanol / 60 °C / 45004.5 Torr View Scheme |
4-amino-3-phenylbutanoic acid
2-Fluorobenzaldehyde
methyl 2,4-dioxopentanoate
Conditions | Yield |
---|---|
In ethanol; water at 20℃; for 12h; Condensation; | 78% |
di-tert-butyl dicarbonate
4-amino-3-phenylbutanoic acid
4-((tert-butoxycarbonyl)amino)-3-phenylbutanoic acid
Conditions | Yield |
---|---|
With sodium hydroxide In water; tert-butyl alcohol at 0 - 20℃; | 73% |
Conditions | Yield |
---|---|
With thionyl chloride at 0 - 20℃; for 16h; | 66% |
4-amino-3-phenylbutanoic acid
N,N'-diisopropyl-O-methylisourea
C13H19NO2
Conditions | Yield |
---|---|
In methanol for 120h; Ambient temperature; | 65% |
Conditions | Yield |
---|---|
In ethanol for 3h; Reflux; | 62% |
Conditions | Yield |
---|---|
With potassium hydroxide |
4-amino-3-phenylbutanoic acid
(RS)-2-(2-oxo-4-phenylpyrrolidin-1-yl)acetamide
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: potassium hydroxide / ethanol / 65 - 75 °C 2: ethanol / 65 - 75 °C 3: acetic acid / ethanol 4: Heating View Scheme |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: potassium hydroxide / ethanol / 65 - 75 °C 2: ethanol / 65 - 75 °C 3: acetic acid / ethanol View Scheme |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: potassium hydroxide / ethanol / 65 - 75 °C 2: ethanol / 65 - 75 °C 3: acetic acid / ethanol 4: sodium hydroxide / ethanol / 65 - 75 °C 5: ethanol / 65 - 75 °C View Scheme |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol at 65 - 75℃; |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: potassium hydroxide / ethanol / 65 - 75 °C 2: ethanol / 65 - 75 °C View Scheme |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: potassium hydroxide / ethanol / 65 - 75 °C 2: ethanol / 65 - 75 °C 3: acetic acid / ethanol 4: sodium hydroxide / ethanol / 65 - 75 °C View Scheme |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: sodium hydroxide / water; tert-butyl alcohol / 0 - 20 °C 2.1: potassium carbonate / tetrahydrofuran / 0.25 h / 20 °C 2.2: 20 °C 3.1: hydrogenchloride / ethyl acetate / 3 h / 20 °C 4.1: triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 20 °C 5.1: sodium hydroxide / 3 h / 20 °C 6.1: borane-THF / tetrahydrofuran / 3 h / 20 °C / Inert atmosphere View Scheme |
4-amino-3-phenylbutanoic acid
tert-butyl (3-amino-2-phenylpropyl)carbamate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: ethanol / 3 h / Reflux 2: triethylamine; diphenyl phosphoryl azide / 1,4-dioxane / 100 °C 3: hydrazine hydrate / ethanol / 2 h / 80 °C View Scheme |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: ethanol / 3 h / Reflux 2.1: triethylamine; diphenyl phosphoryl azide / 1,4-dioxane / 100 °C 3.1: hydrazine hydrate / ethanol / 2 h / 80 °C 4.1: sodium hydrogencarbonate / dichloromethane / 0.17 h / 20 °C 4.2: 1 h / 20 °C View Scheme |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: ethanol / 3 h / Reflux 2.1: triethylamine; diphenyl phosphoryl azide / 1,4-dioxane / 100 °C 3.1: hydrazine hydrate / ethanol / 2 h / 80 °C 4.1: sodium hydrogencarbonate / dichloromethane / 0.17 h / 20 °C 4.2: 1 h / 20 °C 5.1: hydrogenchloride / ethyl acetate / 2 h / 20 °C View Scheme |
4-amino-3-phenylbutanoic acid
methyl 4-amino-3-phenylbutanoate hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: sodium hydroxide / water; tert-butyl alcohol / 0 - 20 °C 2.1: potassium carbonate / tetrahydrofuran / 0.25 h / 20 °C 2.2: 20 °C 3.1: hydrogenchloride / ethyl acetate / 3 h / 20 °C View Scheme |
4-amino-3-phenylbutanoic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: sodium hydroxide / water; tert-butyl alcohol / 0 - 20 °C 2.1: potassium carbonate / tetrahydrofuran / 0.25 h / 20 °C 2.2: 20 °C 3.1: hydrogenchloride / ethyl acetate / 3 h / 20 °C 4.1: triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 20 °C View Scheme |
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