1-(2-methoxyphenyl)propan-2-one
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With ammonia; hydrogen In tetrahydrofuran at 120℃; for 15h; | 88% |
With ammonium formate; palladium on activated charcoal In methanol at 20℃; | 75% |
With palladium 10% on activated carbon; ammonium formate In methanol; water at 20℃; | 65% |
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane; water Reflux; | 88% |
(E)-1-(2-methoxyphenyl)prop-1-ene
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With terephthalonitrile; 1,3,5-triphenylbenzene; ammonia In water; acetonitrile Irradiation; | 75% |
With benzene-1,3-dicarbonitrile; 1,3,5-triphenylbenzene; ammonia In water; acetonitrile for 4h; Irradiation; | 75% |
1-(2-bromophenyl)propane-2-one
ammonium formate
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
at 160 - 190℃; und anschliessend mit wss.HCl; |
3-(2-methoxy-phenyl)-2-methyl-propionic acid amide
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With potassium hydroxide; bromine anschliessend Erwaermen des mit Natriumhydroxid versetzten Reaktionsgemisches; |
1-(2-methoxyphenyl)-2-nitropropene
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride | |
With lithium aluminium tetrahydride In tetrahydrofuran for 4h; Inert atmosphere; Reflux; |
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With methanol; ammonia at 110℃; |
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
ortho-anisaldehyde
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2.) p-toluenesulfonic acid 2: 75 percent / m-dicyanobenzene, NH3, 1,3,5-triphenylbenzene / acetonitrile; H2O / 4 h / Irradiation View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / 2 h / Reflux 2: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 °C / Reflux View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / 2 h / Inert atmosphere; Reflux 2: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / Inert atmosphere; Reflux View Scheme |
3-(2-methoxyphenyl)-2-methylacrylic acid
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: platinum; acetic acid / Hydrogenation 2: chloroform; sodium hydroxide; aqueous ammonia; thionyl chloride 3: bromine; aqueous KOH-solution / anschliessend Erwaermen des mit Natriumhydroxid versetzten Reaktionsgemisches View Scheme |
rac-3-(2-methoxyphenyl)-2-methylpropanoic acid
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: chloroform; sodium hydroxide; aqueous ammonia; thionyl chloride 2: bromine; aqueous KOH-solution / anschliessend Erwaermen des mit Natriumhydroxid versetzten Reaktionsgemisches View Scheme |
1-(2'-methoxyphenyl)-2-nitropropane
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 3h; Reflux; |
2-allylanisole
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium 2,2,2-trifluoroacetate; iron(III) chloride; palladium(II) trifluoroacetate / acetonitrile; water / 60 °C / Inert atmosphere; Darkness 2: pyridoxal 5'-phosphate; isopropylamine; amine transaminase TA-P2-B01 / aq. phosphate buffer / 24 h / 30 °C / pH 7.5 / Enzymatic reaction View Scheme |
formaldehyd
(d,l)-2-methoxyamphetamine
[2-(2-methoxyphenyl)-1-methylethylamino]acetonitrile
Conditions | Yield |
---|---|
With hydrogenchloride In water at 0 - 20℃; pH=2 - 3; | 91% |
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With iodine; silver sulfate In ethanol for 17h; Ambient temperature; | 83% |
(d,l)-2-methoxyamphetamine
trifluoroacetic anhydride
(+/-)-N-trifluoroacetyl-1-(2-methoxyphenyl)-2-aminopropane
Conditions | Yield |
---|---|
In benzene for 2h; Heating; | 67% |
(E)-3-phenylpropenal
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
With platinum Hydrogenation; |
formaldehyd
(d,l)-2-methoxyamphetamine
[2-(2-methoxy-phenyl)-1-methyl-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With ethanol; sodium acetate; nickel Hydrogenation; |
(d,l)-2-methoxyamphetamine
1-(2-methoxyphenyl)propan-2-one
bis-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-amine
Conditions | Yield |
---|---|
With methanol; platinum Hydrogenation; isomer(ic) II; | |
With methanol; platinum Hydrogenation; isomer(ic) II; |
(d,l)-2-methoxyamphetamine
2-(2-Amino-propyl)-phenol
Conditions | Yield |
---|---|
With hydrogenchloride at 160℃; |
(d,l)-2-methoxyamphetamine
2-phenylethyl chloride
Conditions | Yield |
---|---|
With ethanol at 120℃; |
(d,l)-2-methoxyamphetamine
benzaldehyde
Conditions | Yield |
---|---|
With ethanol |
(d,l)-2-methoxyamphetamine
phenyl isothiocyanate
(d,l)-2-methoxyamphetamine
benzenesulfonyl chloride
Conditions | Yield |
---|---|
With sodium hydroxide |
(d,l)-2-methoxyamphetamine
acetic anhydride
N-Acetyl-2-methoxyamphenamine
Conditions | Yield |
---|---|
With pyridine |
formaldehyd
(d,l)-2-methoxyamphetamine
potassium cyanide
phenol
Conditions | Yield |
---|---|
(i), (ii) /BRN= 969616/, AlCl3; Multistep reaction; |
(d,l)-2-methoxyamphetamine
ethyl acetate
Conditions | Yield |
---|---|
With Candida antarctica lipase B at 28℃; for 8h; |
(d,l)-2-methoxyamphetamine
1-(2-methoxyphenyl)propan-2-one
Conditions | Yield |
---|---|
In toluene for 6h; Heating; |
(d,l)-2-methoxyamphetamine
1-phenyl-acetone
Conditions | Yield |
---|---|
In toluene for 6h; Heating; |
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 67 percent / benzene / 2 h / Heating 2: 24 percent / TiCl4 / CH2Cl2 / 72 h / 20 °C 3: 99 percent / H2; AcOH; 70percent aq. HClO4 / 10percent Pd/C / 5.5 h / 20 °C / 2327.23 Torr 4: 15percent aq. NaOH / methanol / 2 h / Heating View Scheme |
(d,l)-2-methoxyamphetamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 67 percent / benzene / 2 h / Heating 2: 24 percent / TiCl4 / CH2Cl2 / 72 h / 20 °C 3: 99 percent / H2; AcOH; 70percent aq. HClO4 / 10percent Pd/C / 5.5 h / 20 °C / 2327.23 Torr View Scheme |
(d,l)-2-methoxyamphetamine
(+/-)-N-trifluoroacetyl-1-[2-methoxy-5-(3-phenyl-1-propionyl)phenyl]-2-aminopropane
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 67 percent / benzene / 2 h / Heating 2: 24 percent / TiCl4 / CH2Cl2 / 72 h / 20 °C View Scheme |
(d,l)-2-methoxyamphetamine
methoxyphenamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: ethanol 2: anschliessend Behandeln mit wss. Methanol View Scheme |
(d,l)-2-methoxyamphetamine
ethyl-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-amine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: ethanol 2: anschliessend Behandeln mit wss. Methanol View Scheme |
The 1-(2-Methoxyphenyl)-2-propylamine with the cas number 15402-84-3 is also called Benzeneethanamine,2-methoxy-a-methyl-. Both the systematic name and IUPAC name are 1-(2-methoxyphenyl)propan-2-amine. Its molecular formula is C10H15NO. This chemical is a kind of organics. It should be stored in dry and cool environment.
The properties of the chemical are: (1)ACD/LogP: 1.72; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.36; (4)ACD/LogD (pH 7.4): -0.76; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 2; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 4; (12)Polar Surface Area: 12.47 Å2; (13)Index of Refraction: 1.518; (14)Molar Refractivity: 50.6 cm3; (15)Molar Volume: 166.8 cm3; (16)Polarizability: 20.06×10-24cm3; (17)Surface Tension: 35.3 dyne/cm; (18)Enthalpy of Vaporization: 48.38 kJ/mol; (19)Vapour Pressure: 0.0268 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES: O(c1ccccc1CC(N)C)C
(2)InChI: InChI=1/C10H15NO/c1-8(11)7-9-5-3-4-6-10(9)12-2/h3-6,8H,7,11H2,1-2H3
(3)InChIKey: VBAHFEPKESUPDE-UHFFFAOYAE
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