DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:5339-85-5
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inquiryHigh purity CAS 5339-85-5 2-Aminophenethanol in stock Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediates (Fl
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
2-aminophenethyl alcoholAppearance:Colorless transparent liquid Storage:Keep away of light, cool place Package:according to customers' requirements Application:pharmaceutical intermediates Transportation:By air(EMS or EUB or FedEx or TNT ect...) or b
Superior quality, moderate price & quick delivery. Appearance:white crystals Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:For medicine , pesticide intermed
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2-Aminophenethanol Chemical Properties Melting point 140-145 °C Boiling point 147-148 °C/3.5 mmHg (lit.) density 1.045 g/mL at 25 °C (lit.) refractive index n20/D 1.588(lit.) Fp >230 °F pka 14.81±0.10(
Cas:5339-85-5
Min.Order:1 Gram
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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
Cas:5339-85-5
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High quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
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Cas:5339-85-5
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inquiryhigh quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
2-nitro-benzeneethanol
2-aminophenethyl alcohol
Conditions | Yield |
---|---|
100% | |
100% | |
100% |
Conditions | Yield |
---|---|
With hydrogen; palladium/alumina |
Conditions | Yield |
---|---|
With N-benzyl-trimethylammonium hydroxide; calcium chloride; zinc 1.) Me2SO, 95 deg C, 1 h, 2.) H2O, reflux; Multistep reaction; |
Conditions | Yield |
---|---|
With 1-Methylpyrrolidine; selenium In tetrahydrofuran at 150℃; under 22800 Torr; for 5h; | A n/a B 66 % Chromat. |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 37 percent / sodium phenoxide / dimethylsulfoxide / 1 h / 60 - 67 °C 2: 78 percent / calcium chloride; zinc powder / H2O / 0.5 h / Heating View Scheme | |
Multi-step reaction with 2 steps 1: sodium hydroxide / 1.5 h / pH 7.4 / Large scale reaction 2: hydrogen / paraffin oil / 1.5 h / 110 °C / 15001.5 Torr View Scheme | |
Multi-step reaction with 2 steps 1: sodium phenoxide / dimethyl sulfoxide / 1 h / 60 - 67 °C 2: zinc; calcium chloride / water / 0.5 h / Reflux View Scheme | |
Multi-step reaction with 2 steps 1: potassium hydroxide / water; dimethyl sulfoxide / 1 h / 0 - 20 °C / Inert atmosphere 2: hydrogen; palladium 10% on activated carbon / methanol / 20.5 h / 20 °C / 760.05 Torr / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: acetic acid anhydride; nitric acid / 35 - 40 °C / Kochen des Reaktionsprodukts mit methanol. HCl 2: zinc; aqueous calcium chloride View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: borane-THF 2: zinc; calcium chloride; water View Scheme | |
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / methanol 2: 10% Pd/C; hydrogen / ethanol View Scheme |
Conditions | Yield |
---|---|
With tris(2,4-pentanedionato)ruthenium(III); ytterbium(III) trifluoromethanesulfonate nonohydrate; hydrogen; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In tetrahydrofuran at 150℃; under 37503.8 Torr; for 15h; Autoclave; | A 61 %Chromat. B n/a |
methyl (2-nitrophenyl)acetate
A
indole
B
2-oxoindole
C
2-aminophenethyl alcohol
D
2-aminophenylacetic acid methyl ester
Conditions | Yield |
---|---|
With sodium tetrahydroborate In tetrahydrofuran; water at 20℃; for 12h; Sonication; chemoselective reaction; |
Conditions | Yield |
---|---|
100% | |
100% | |
With C21H28I3IrN6Pd; potassium hydroxide In toluene at 110℃; for 2h; Reagent/catalyst; Inert atmosphere; Schlenk technique; | 99% |
2-aminophenethyl alcohol
2-tert-butyldiphenylsilyloxyethylaniline
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 0℃; for 17h; | 100% |
5-bromovaleroyl chloride
2-aminophenethyl alcohol
5-bromo-N-[2-(2-hydroxyethyl)phenyl]pentanamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -5 - 0℃; | 100% |
With triethylamine In dichloromethane at -5 - 0℃; | 100% |
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 2h; Heating; | 97% |
triethylsilyl chloride
2-aminophenethyl alcohol
O-triethylsilyl-2-(o-aminophenyl)ethanol
Conditions | Yield |
---|---|
With triethylamine | 97% |
With triethylamine In dichloromethane at -20℃; for 1h; | 97% |
2-aminophenethyl alcohol
2-benzoyl-4,5-dichloropyridazin-3(2H)-one
benzoic acid-[2-(2-hydroxy-ethyl)-anilide]
Conditions | Yield |
---|---|
In tetrahydrofuran at 18℃; for 18h; | 97% |
2-aminophenethyl alcohol
trifluoroacetic acid
2,2,2-trifluoro-1-(indolin-1-yl)ethan-1-one
Conditions | Yield |
---|---|
With tetrachloromethane; triethylamine; triphenylphosphine Heating; | 97% |
2-aminophenethyl alcohol
carbonic acid dimethyl ester
2,3-dihydroindole-1-carboxylic acid methyl ester
Conditions | Yield |
---|---|
With 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine at 90℃; for 21h; Reagent/catalyst; Time; | 97% |
Conditions | Yield |
---|---|
Stage #1: 2-aminophenethyl alcohol With thionyl chloride In 1,2-dimethoxyethane at 20℃; Stage #2: In 1,2-dimethoxyethane; water at 60℃; Further stages.; | 94% |
With sodium hydroxide; benzenesulfonyl chloride | |
With zinc(II) chloride at 200℃; |
2-aminophenethyl alcohol
2-acetyl-4,5-dichloropyridazin-3(2H)-one
2-(2-acetylaminophenyl)ethyl alcohol
Conditions | Yield |
---|---|
In tetrahydrofuran at 17℃; for 0.2h; | 94% |
2-aminophenethyl alcohol
2,3-Dioxo-pent-4-enoic acid tert-butyl ester
Conditions | Yield |
---|---|
94% |
Conditions | Yield |
---|---|
With tetrachloromethane; triethylamine; triphenylphosphine Heating; | 94% |
5-chloro-1H-Indole-2-carboxylic acid
2-aminophenethyl alcohol
C17H15ClN2O2
Conditions | Yield |
---|---|
With 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 14h; | 94% |
2-aminophenethyl alcohol
4-methyl-benzaldehyde
2-(4-methylphenyl)quinoline
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; silver trifluoromethanesulfonate In toluene at 120℃; for 12h; Green chemistry; | 94% |
Conditions | Yield |
---|---|
In benzene for 0.5h; Heating; | 93% |
2-aminophenethyl alcohol
4,5-Dichloro-2-(4-methoxy-benzoyl)-2H-pyridazin-3-one
Conditions | Yield |
---|---|
In tetrahydrofuran at 18℃; for 7h; | 93% |
3-(3-hydroxy-6-methylpyridin-2-ylmethyl)-2-(3-morpholin-4-ylpropylamino)-3H-benzoimidazole-5-carbaldehyde
2-aminophenethyl alcohol
Conditions | Yield |
---|---|
With acetic acid In methanol at 20℃; for 16h; | 93% |
2-isocyanobenzaldehyde
2-aminophenethyl alcohol
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In dimethyl sulfoxide at 25℃; Molecular sieve; | 93% |
Conditions | Yield |
---|---|
With [RuCl2(2-diphenylphosphinoethylamine)2]; potassium tert-butylate; zinc(II) trifluoroacetate In 1,4-dioxane for 18h; Reagent/catalyst; Reflux; | 91% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0 - 25℃; | 91% |
di-tert-butyl dicarbonate
2-aminophenethyl alcohol
2-(2-((tert-butoxycarbonyl)amino)phenyl)ethanol
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In 1,4-dioxane; water for 4h; Ambient temperature; | 90% |
With sodium hydrogencarbonate In 1,4-dioxane | 72% |
With sodium hydrogencarbonate In 1,4-dioxane; water at 20℃; |
Burgess Reagent
2-aminophenethyl alcohol
Conditions | Yield |
---|---|
In tetrahydrofuran for 2h; Heating; | 90% |
2-aminophenethyl alcohol
Conditions | Yield |
---|---|
In tetrahydrofuran for 2h; Heating / reflux; | 90% |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; silver trifluoromethanesulfonate In toluene at 120℃; for 12h; Green chemistry; | 89% |
Multi-step reaction with 2 steps 1: 0.08 h / 100 °C 2: silver trifluoromethanesulfonate; trifluorormethanesulfonic acid; oxygen / toluene / 12 h / 120 °C View Scheme |
Conditions | Yield |
---|---|
With potassium hydroxide | 88% |
With potassium hydroxide at 180℃; under 0.25 Torr; for 4h; | 78% |
With potassium hydroxide at 180℃; under 0.05 Torr; for 4h; | 75% |
Conditions | Yield |
---|---|
With sulfuric acid In isopropyl alcohol at 25℃; for 4h; UV-irradiation; | 87% |
2-aminophenethyl alcohol
methyl iodide
2-(2-dimethylaminophenyl)ethyl alcohol
Conditions | Yield |
---|---|
Stage #1: 2-aminophenethyl alcohol With potassium carbonate In acetonitrile at 20℃; for 0.666667h; Stage #2: methyl iodide In acetonitrile for 3h; Reflux; | 86.3% |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; silver trifluoromethanesulfonate In toluene at 120℃; for 12h; Green chemistry; | 84% |
Conditions | Yield |
---|---|
With tetrachloromethane; triethylamine; triphenylphosphine Heating; | 83% |
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