Product Name

  • Name

    N-desmethylmethoxyphenamine

  • EINECS
  • CAS No. 15402-84-3
  • Article Data16
  • CAS DataBase
  • Density 0.99g/cm3
  • Solubility
  • Melting Point
  • Formula C10H15NO
  • Boiling Point 246.7°C at 760 mmHg
  • Molecular Weight 165.235
  • Flash Point 98.1°C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 15402-84-3 (N-desmethylmethoxyphenamine)
  • Hazard Symbols
  • Synonyms Phenethylamine,o-methoxy-a-methyl- (6CI,7CI,8CI);1-(2-Methoxyphenyl)-2-aminopropane;2-Methoxy(phenylisopropyl)amine;2-Methoxyamphetamine;N-Demethylmethoxyphenamine;N-Desmethylmethoxyphenamine;o-Methoxy(phenylisopropyl)amine;o-Methoxy-a-methylphenethylamine;o-Methoxyamphetamine;
  • PSA 35.25000
  • LogP 2.28520

Synthetic route

1-(2-methoxyphenyl)propan-2-one
5211-62-1

1-(2-methoxyphenyl)propan-2-one

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
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%
N-(1-(2-methoxyphenyl)propan-2-yl)formamide

N-(1-(2-methoxyphenyl)propan-2-yl)formamide

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
With hydrogenchloride In 1,4-dioxane; water Reflux;88%
(E)-1-(2-methoxyphenyl)prop-1-ene
2077-36-3

(E)-1-(2-methoxyphenyl)prop-1-ene

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
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
21906-31-0

1-(2-bromophenyl)propane-2-one

ammonium formate
540-69-2

ammonium formate

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
at 160 - 190℃; und anschliessend mit wss.HCl;
3-(2-methoxy-phenyl)-2-methyl-propionic acid amide
858783-40-1

3-(2-methoxy-phenyl)-2-methyl-propionic acid amide

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
With potassium hydroxide; bromine anschliessend Erwaermen des mit Natriumhydroxid versetzten Reaktionsgemisches;
1-(2-methoxyphenyl)-2-nitropropene
6306-34-9

1-(2-methoxyphenyl)-2-nitropropene

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
With lithium aluminium tetrahydride
With lithium aluminium tetrahydride In tetrahydrofuran for 4h; Inert atmosphere; Reflux;
(+-)-2-<2-bromo-propyl>-anisole

(+-)-2-<2-bromo-propyl>-anisole

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
With methanol; ammonia at 110℃;
2-<2-bromo-propenyl>-anisole

2-<2-bromo-propenyl>-anisole

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
With lithium aluminium tetrahydride; diethyl ether
ortho-anisaldehyde
135-02-4

ortho-anisaldehyde

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
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
3368-15-8

3-(2-methoxyphenyl)-2-methylacrylic acid

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
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
52427-12-0

rac-3-(2-methoxyphenyl)-2-methylpropanoic acid

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
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
34322-76-4

1-(2'-methoxyphenyl)-2-nitropropane

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 3h; Reflux;
2-allylanisole
3698-28-0

2-allylanisole

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

Conditions
ConditionsYield
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
potassium cyanide

potassium cyanide

formaldehyd
50-00-0

formaldehyd

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

[2-(2-methoxyphenyl)-1-methylethylamino]acetonitrile
1161921-16-9

[2-(2-methoxyphenyl)-1-methylethylamino]acetonitrile

Conditions
ConditionsYield
With hydrogenchloride In water at 0 - 20℃; pH=2 - 3;91%
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

5-iodo-2-methoxyamphetamine

5-iodo-2-methoxyamphetamine

Conditions
ConditionsYield
With iodine; silver sulfate In ethanol for 17h; Ambient temperature;83%
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

trifluoroacetic anhydride
407-25-0

trifluoroacetic anhydride

(+/-)-N-trifluoroacetyl-1-(2-methoxyphenyl)-2-aminopropane
370884-68-7

(+/-)-N-trifluoroacetyl-1-(2-methoxyphenyl)-2-aminopropane

Conditions
ConditionsYield
In benzene for 2h; Heating;67%
(E)-3-phenylpropenal
14371-10-9

(E)-3-phenylpropenal

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

[2-(2-methoxy-phenyl)-1-methyl-ethyl]-(3-phenyl-propyl)-amine

[2-(2-methoxy-phenyl)-1-methyl-ethyl]-(3-phenyl-propyl)-amine

Conditions
ConditionsYield
With platinum Hydrogenation;
formaldehyd
50-00-0

formaldehyd

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

[2-(2-methoxy-phenyl)-1-methyl-ethyl]-dimethyl-amine
71861-16-0

[2-(2-methoxy-phenyl)-1-methyl-ethyl]-dimethyl-amine

Conditions
ConditionsYield
With ethanol; sodium acetate; nickel Hydrogenation;
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

1-(2-methoxyphenyl)propan-2-one
5211-62-1

1-(2-methoxyphenyl)propan-2-one

bis-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-amine
47302-54-5

bis-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-amine

Conditions
ConditionsYield
With methanol; platinum Hydrogenation; isomer(ic) II;
With methanol; platinum Hydrogenation; isomer(ic) II;
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

2-(2-Amino-propyl)-phenol
87835-14-1

2-(2-Amino-propyl)-phenol

Conditions
ConditionsYield
With hydrogenchloride at 160℃;
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

2-phenylethyl chloride
622-24-2

2-phenylethyl chloride

[2-(2-methoxy-phenyl)-1-methyl-ethyl]-phenethyl-amine

[2-(2-methoxy-phenyl)-1-methyl-ethyl]-phenethyl-amine

Conditions
ConditionsYield
With ethanol at 120℃;
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

benzaldehyde
100-52-7

benzaldehyde

benzylidene-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-amine

benzylidene-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-amine

Conditions
ConditionsYield
With ethanol
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

phenyl isothiocyanate
103-72-0

phenyl isothiocyanate

N-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-N'-phenyl-thiourea

N-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-N'-phenyl-thiourea

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

benzenesulfonyl chloride
98-09-9

benzenesulfonyl chloride

N-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-benzenesulfonamide

N-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-benzenesulfonamide

Conditions
ConditionsYield
With sodium hydroxide
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

acetic anhydride
108-24-7

acetic anhydride

N-Acetyl-2-methoxyamphenamine
72687-66-2

N-Acetyl-2-methoxyamphenamine

Conditions
ConditionsYield
With pyridine
formaldehyd
50-00-0

formaldehyd

(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

potassium cyanide
151-50-8

potassium cyanide

phenol
108-95-2

phenol

1-(4-Hydroxy-phenyl)-2-[2-(2-methoxy-phenyl)-1-methyl-ethylamino]-ethanone

1-(4-Hydroxy-phenyl)-2-[2-(2-methoxy-phenyl)-1-methyl-ethylamino]-ethanone

Conditions
ConditionsYield
(i), (ii) /BRN= 969616/, AlCl3; Multistep reaction;
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

ethyl acetate
141-78-6

ethyl acetate

A

(S)-1-(o-methoxyphenyl)propan-2-amine

(S)-1-(o-methoxyphenyl)propan-2-amine

B

(R)-1-(o-methoxyphenyl)propan-2-amine

(R)-1-(o-methoxyphenyl)propan-2-amine

C

(R)-N-[1-(o-methoxyphenyl)propan-2-yl]ethanamide

(R)-N-[1-(o-methoxyphenyl)propan-2-yl]ethanamide

Conditions
ConditionsYield
With Candida antarctica lipase B at 28℃; for 8h;
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

1-(2-methoxyphenyl)propan-2-one
5211-62-1

1-(2-methoxyphenyl)propan-2-one

N-[2-(2-methoxyphenyl)-1-methylethyl]-N-[2-(2-methoxyphenyl)-1-methylethylidene]amine

N-[2-(2-methoxyphenyl)-1-methylethyl]-N-[2-(2-methoxyphenyl)-1-methylethylidene]amine

Conditions
ConditionsYield
In toluene for 6h; Heating;
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

1-phenyl-acetone
103-79-7

1-phenyl-acetone

N-[2-(2-methoxyphenyl)-1-methylethyl]-N-[1-methyl-2-phenylethylidene]amine

N-[2-(2-methoxyphenyl)-1-methylethyl]-N-[1-methyl-2-phenylethylidene]amine

Conditions
ConditionsYield
In toluene for 6h; Heating;
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

2-[2-methoxy-5-(3-phenyl-propyl)-phenyl]-1-methyl-ethylamine

2-[2-methoxy-5-(3-phenyl-propyl)-phenyl]-1-methyl-ethylamine

Conditions
ConditionsYield
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
15402-84-3

(d,l)-2-methoxyamphetamine

2,2,2-trifluoro-N-{2-[2-methoxy-5-(3-phenyl-propyl)-phenyl]-1-methyl-ethyl}-acetamide

2,2,2-trifluoro-N-{2-[2-methoxy-5-(3-phenyl-propyl)-phenyl]-1-methyl-ethyl}-acetamide

Conditions
ConditionsYield
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
15402-84-3

(d,l)-2-methoxyamphetamine

(+/-)-N-trifluoroacetyl-1-[2-methoxy-5-(3-phenyl-1-propionyl)phenyl]-2-aminopropane
370884-70-1

(+/-)-N-trifluoroacetyl-1-[2-methoxy-5-(3-phenyl-1-propionyl)phenyl]-2-aminopropane

Conditions
ConditionsYield
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
15402-84-3

(d,l)-2-methoxyamphetamine

methoxyphenamine
93-30-1

methoxyphenamine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: ethanol
2: anschliessend Behandeln mit wss. Methanol
View Scheme
(d,l)-2-methoxyamphetamine
15402-84-3

(d,l)-2-methoxyamphetamine

ethyl-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-amine
91553-50-3

ethyl-[2-(2-methoxy-phenyl)-1-methyl-ethyl]-amine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: ethanol
2: anschliessend Behandeln mit wss. Methanol
View Scheme

1-(2-Methoxyphenyl)-2-propylamine Specification

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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