As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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Cas:55-81-2
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inquiry4-Methoxyphenethylamine CAS:55-81-2 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic inte
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryAppearance:white powder/crystal 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:Common products:Sea/Ai
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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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
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquirylower price and high quality Appearance:white Storage:Preserve In Well-Closed, Light-Resistant and Tight Containers. Store In Cool & Dry Place Package:1g,5g,10g...1kg,5kg...more Application:Pharmaceutical Intermediate Transportation:shipping,land,a
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquiry4-Methoxyphenethylamine Basic information Product Name: 4-Methoxyphenethylamine Synonyms: 2-(4-Methoxyphenyl)ethanamine;4-Methoxy-2-phenethylamine;4-methoxy-benzeneethanamin;4-Methoxybenzeneethanamine;4-Methoxy-beta-phenylethylamine;Homoanisyl
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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
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inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
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inquiryShanghai Massive Chemical Technology Co., Ltd. is engaged in development, production and marketing Specialty Chemicals to satisfy the changing needs of the chemical industry. We specialize in manufacturing high quality of Advanced Intermediates, Sp
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inquirybenzyl 4-methoxyphenethylcarbamate
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol at 20℃; for 1h; | 100% |
Conditions | Yield |
---|---|
With aluminum (III) chloride; lithium aluminium tetrahydride In diethyl ether at 0 - 20℃; | 96% |
With lithium borohydride; diisopropopylaminoborane In tetrahydrofuran for 18h; Reflux; | 94% |
With [Ru(H)(BH4)(CO)(PPh3)(3-(di-tert-butylphosphino)-N-((1-methyl-1H-imidazol-2 yl)methyl)propylamine)]; hydrogen In isopropyl alcohol at 70℃; for 3h; Inert atmosphere; Autoclave; | 94% |
lysichitalexin
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With samarium diiodide; water; isopropylamine In tetrahydrofuran | 96% |
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With potassium carbonate; thiophenol In acetonitrile at 50℃; | 95% |
C12H14Cl3NO3
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
Stage #1: C12H14Cl3NO3 With chloro-trimethyl-silane; mischmetal In tetrahydrofuran for 2h; Inert atmosphere; Reflux; Stage #2: With water In tetrahydrofuran for 0.0833333h; Alkaline conditions; | 87% |
Conditions | Yield |
---|---|
With hydrogenchloride; hydrogen; acetic acid; palladium on activated charcoal for 1h; | 71% |
With hydrogen; carbon palladium at 85℃; under 37503 Torr; | 70% |
(catalytic hydrogenation); |
2-4-methoxyphenylethylcarbamic acid methyl ester
A
7-methoxy-3,4-dihydro-2H-isoquinolin-1-one
B
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With PPA at 145℃; for 0.166667h; | A 59% B 30% |
3-(4-methoxy-phenyl)propionamide
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With sodium hydroxide; bromine In water at 70 - 80℃; for 0.25h; | 53% |
With sodium hypobromide | |
With alkaline sodium hypochlorite |
4-methyl-N-[2-(4-methoxyphenyl)ethyl]benzenesulfonamide
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With titanium tetrachloride In tetrahydrofuran for 2.5h; Heating; | 40% |
(E)-1-methoxy-4-(2-nitrovinyl)benzene
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With samarium diiodide; water; isopropylamine In tetrahydrofuran | 36% |
With sulfuric acid; palladium; acetic acid Hydrogenation; | |
bei der elektrochemischen Reduktion; | |
With lithium aluminium tetrahydride |
Conditions | Yield |
---|---|
With aluminium trichloride |
Conditions | Yield |
---|---|
With chloroform; nitrosylchloride Hydrieren des Reaktionsprodukts an Raney-Nickel in Methanol; | |
Multi-step reaction with 3 steps 1: NOCl, HCl / diethyl ether 2: Et3N / diethyl ether 3: LiAlH4 / diethyl ether View Scheme | |
With D-Glucose; ammonia; oxygen In aq. phosphate buffer at 30℃; for 10h; Green chemistry; regioselective reaction; | |
Multi-step reaction with 3 steps 1: oxygen; styrene monooxygenase / Enzymatic reaction 2: styrene oxide isomerase / Enzymatic reaction 3: ammonia; ω-transaminase; L-alanine dehydrogenase / Enzymatic reaction View Scheme |
4-methoxymandelonitrile
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride; ethanol; platinum Hydrogenation; |
Conditions | Yield |
---|---|
With sodium azide; chloroform; sulfuric acid | |
Multi-step reaction with 2 steps 1: thionyl chloride; chloroform / nachfolgend Behandlung mit Natriumhydroxyd in Ammoniak 2: alkaline sodium hypochlorite View Scheme | |
Multi-step reaction with 3 steps 1: chloroform; PCl5 2: diethyl ether; NH3 3: bromine; NaOH-solution / 55 °C View Scheme |
4-methoxybenzoyl cyanide
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With sulfuric acid; palladium; acetic acid Hydrogenation; |
Conditions | Yield |
---|---|
With sulfuric acid; palladium; acetic acid Hydrogenation; |
acetoxy-(4-methoxy-phenyl)-acetonitrile
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With sulfuric acid; palladium; acetic acid Hydrogenation; |
p-methoxybenzylnitrile
A
4-methoxy-N-[2-(4-methoxyphenyl)ethyl]benzeneethanamine
B
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With nickel Hydrogenation; |
1-(2-Chloroethyl)-4-methoxybenzene
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With ammonia | |
With ethanol; ammonia at 100℃; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether |
2-[2-(4-methoxyphenyl)ethyl]-1H-isoindole-1,3(2H)-dione
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With hydrazine hydrate In methanol at 70℃; |
[2-(4-Methoxy-phenyl)-ethyl]-phosphoramidic acid diethyl ester
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With hydrogenchloride at 80 - 85℃; for 1.5h; Yield given; |
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With sulfuric acid; palladium; acetic acid Hydrogenation; |
4-Methoxyphenethylamine
sulfuric acid
(E)-1-methoxy-4-(2-nitrovinyl)benzene
acetic acid
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
Hydrogenation; |
sulfuric acid
4-methoxybenzoyl cyanide
acetic acid
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
Hydrogenation; |
ethanol
(E)-1-methoxy-4-(2-nitrovinyl)benzene
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
Hydrogenation; |
4-Methoxyphenethylamine
methyl chloroformate
2-4-methoxyphenylethylcarbamic acid methyl ester
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine Inert atmosphere; Cooling with ice; | 100% |
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; | 99% |
With triethylamine In tetrahydrofuran for 24h; Ambient temperature; | 95% |
4-Methoxyphenethylamine
chloroacetyl chloride
2-(4-methoxyphenyl)ethan-1-aminechloroacetate
Conditions | Yield |
---|---|
With potassium carbonate In dichloromethane Ambient temperature; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; for 6h; Reflux; | 85% |
With triethylamine In dichloromethane at 0 - 20℃; for 4h; | 76% |
4-Methoxyphenethylamine
chloroacetic acid
2-(4-methoxyphenyl)ethan-1-aminechloroacetate
Conditions | Yield |
---|---|
Stage #1: 4-Methoxyphenethylamine; 4-formyl-3,5-dimethoxyphenoxy-Merrifield resin With sodium tris(acetoxy)borohydride In acetic acid; N,N-dimethyl-formamide at 20℃; for 69h; Solid phase reaction; reductive amination; Stage #2: chloroacetic acid With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 15h; Solid phase reaction; acylation; Stage #3: With dimethylsulfide; water; trifluoroacetic acid In dichloromethane at 20℃; for 15h; Solid phase reaction; cleavage of amide; | 100% |
Conditions | Yield |
---|---|
Stage #1: 4-Methoxyphenethylamine; 4-formyl-3,5-dimethoxyphenoxy-Merrifield resin With sodium tris(acetoxy)borohydride In acetic acid; N,N-dimethyl-formamide at 20℃; for 69h; Solid phase reaction; reductive amination; Stage #2: butyric acid With benzotriazol-1-ol; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 15h; Solid phase reaction; acylation; Stage #3: With dimethylsulfide; water; trifluoroacetic acid In dichloromethane at 20℃; for 15h; Solid phase reaction; cleavage of amide; | 100% |
4-Methoxyphenethylamine
piperidine-1,4-dicarboxylic acid mono-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-1,1-dimethylundecyl) ester
4-[2-(4-methoxy-phenyl)-ethylcarbamoyl]-piperidine-1-carboxylic acid 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-1,1-dimethyl-undecyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In chloroform; N,N-dimethyl-formamide at 20℃; for 16h; | 100% |
di-tert-butyl dicarbonate
4-Methoxyphenethylamine
N-(tert-butoxycarbonyl)-2-(4-methoxyphenyl)-ethylamine
Conditions | Yield |
---|---|
With guanidine hydrochloride In ethanol at 35 - 40℃; for 0.0166667h; | 100% |
With sulfonic acid-functionalized nanoporous titania catalyst In neat (no solvent) at 20℃; for 0.266667h; chemoselective reaction; | 96% |
With triethylamine In dichloromethane at 20℃; for 1h; | 96% |
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine In N,N-dimethyl-formamide at 20℃; for 18h; | 99.94% |
acetic anhydride
4-Methoxyphenethylamine
N-(4-methoxyphenylethyl)acetamide
Conditions | Yield |
---|---|
at 20 - 30℃; for 1h; | 99% |
With triethylamine In dichloromethane for 2h; Ambient temperature; | 86% |
With triethylamine In dichloromethane at 20℃; | 85% |
chloroformic acid ethyl ester
4-Methoxyphenethylamine
ethyl-N-<2-(4-methoxyphenyl)ethyl>-carbamate
Conditions | Yield |
---|---|
With potassium carbonate In tetrahydrofuran at 25℃; | 99% |
With pyridine In dichloromethane at 0 - 20℃; | 99% |
With triethylamine In dichloromethane at 0 - 25℃; for 1h; | 98.3% |
N-((tert-butyloxy)carbonyl)iminodiacetic acid
4-Methoxyphenethylamine
N-((tert-butyloxy)carbonyl)-N'-(2-(4-methoxyphenyl)ethyl)iminodiacetic acid monoamide
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 25℃; for 20h; Substitution; | 99% |
4-Methoxyphenethylamine
2-methoxy-5-chlorobenzoyl chloride
5-chloro-2-methoxy-N-(2-(4-methoxyphenyl)ethyl)benzamide
Conditions | Yield |
---|---|
With pyridine at 20℃; for 1h; | 99% |
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; 4-Methoxyphenethylamine In isopropyl alcohol at 20℃; for 6h; Stage #2: phenylpropynoic acid ethyl ester; tributylphosphine In isopropyl alcohol at 20℃; Further stages.; | 99% |
(3,4-Dimethoxyphenyl)acetic acid
4-Methoxyphenethylamine
2-(3,4-dimethoxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]acetamide
Conditions | Yield |
---|---|
In neat (no solvent) at 150℃; for 0.5h; Microwave irradiation; | 99% |
In 5,5-dimethyl-1,3-cyclohexadiene for 16h; Reflux; Inert atmosphere; | 94% |
4-chlorophenylacetic Acid
4-Methoxyphenethylamine
2-(4-chlorophenyl)-N-[2-(4-methoxyphenyl)ethyl]acetamide
Conditions | Yield |
---|---|
In neat (no solvent) at 150℃; for 0.5h; Microwave irradiation; | 99% |
4-Methoxyphenylacetic acid
4-Methoxyphenethylamine
2-(4-methoxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]acetamide
Conditions | Yield |
---|---|
In neat (no solvent) at 150℃; for 0.5h; Microwave irradiation; | 99% |
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine |
3,4,5-trimethoxyphenyl acetic acid
4-Methoxyphenethylamine
N-[2-(4-methoxyphenyl)ethyl]-2-(3,4,5-trimethoxyphenyl)acetamide
Conditions | Yield |
---|---|
In neat (no solvent) at 150℃; for 0.5h; Microwave irradiation; | 99% |
4-Methoxyphenethylamine
2-naphthylacetic acid
N-[2-(4-methoxyphenyl)ethyl]-2-(naphthalen-2-yl)acetamide
Conditions | Yield |
---|---|
In neat (no solvent) at 150℃; for 0.5h; Microwave irradiation; | 99% |
girard's reagent T
4-Methoxyphenethylamine
A
1-hydroxy-pyrrolidine-2,5-dione
B
diisopropyl (2-((4-methoxyphenethyl)amino)-2-oxoethyl)phosphonate
Conditions | Yield |
---|---|
Stage #1: 2,5-dioxopyrrolidin-1-yl 2-(diisopropoxyphosphoryl)acetate; 4-Methoxyphenethylamine In dichloromethane at 20℃; for 4h; Stage #2: girard's reagent T In methanol; dichloromethane | A n/a B 99% C n/a |
4-Methoxyphenethylamine
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; | 99% |
3,3,3-triphenylpropionyl chloride
4-Methoxyphenethylamine
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 48h; | 98.9% |
Conditions | Yield |
---|---|
Stage #1: caffeic acid With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 0.25h; Cooling with ice; Stage #2: 4-Methoxyphenethylamine In N,N-dimethyl-formamide at 20℃; | 98.8% |
Conditions | Yield |
---|---|
Stage #1: 3,4-(methylenedioxy)cinnamic acid With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide for 0.25h; Cooling with ice; Stage #2: 4-Methoxyphenethylamine In N,N-dimethyl-formamide at 20℃; | 98.4% |
4-Methoxyphenethylamine
2-(4-methoxycyclohexa-1,4-dienyl)ethylamine
Conditions | Yield |
---|---|
With ammonia; sodium In tetrahydrofuran; ethanol at -78℃; Birch reduction; | 98% |
With ammonia; lithium In tert-butyl alcohol at -78℃; for 6h; | 95% |
With ammonia; lithium In ethanol at -78℃; for 15h; | 94% |
4-Methoxyphenethylamine
p-toluenesulfonyl chloride
4-methyl-N-[2-(4-methoxyphenyl)ethyl]benzenesulfonamide
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 2h; Tosylation; | 98% |
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 2h; | 93% |
Stage #1: 4-Methoxyphenethylamine With sodium carbonate In water for 0.5h; pH=8 - 9; Stage #2: p-toluenesulfonyl chloride In water | 91% |
1-(4-chlorophenyl)cyclobutane-1-carboxylic acid
4-Methoxyphenethylamine
1-(4-chlorophenyl)-N-[2-(4-methoxyphenyl)ethyl]cyclobutanecarboxamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 3 - 20℃; | 98% |
1,3-benzodioxole-5-acetic acid
4-Methoxyphenethylamine
2-(2H-1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]acetamide
Conditions | Yield |
---|---|
In neat (no solvent) at 150℃; for 0.5h; Microwave irradiation; | 98% |
In 5,5-dimethyl-1,3-cyclohexadiene for 16h; Reflux; Inert atmosphere; | 80% |
4-Methoxyphenethylamine
marinacarboline A
Conditions | Yield |
---|---|
With triethylamine; diethyl dicarbonate In N,N-dimethyl-formamide at -10 - 20℃; Inert atmosphere; | 98% |
With diethyl cyanophosphonate; triethylamine In N,N-dimethyl-formamide at -10 - 25℃; for 12.5h; | 96% |
phenyl isothiocyanate
4-Methoxyphenethylamine
1-(2-(4-methoxyphenyl)ethyl)-3-phenylthiourea
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 98% |
(2R,3R,4R)-1,3,4-tris(benzyloxy)hexane-2,5-diethylsulfonate
4-Methoxyphenethylamine
(2S,3S,4R)-1-(4-methoxyphenethyl)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine
Conditions | Yield |
---|---|
at 80 - 90℃; | 98% |
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