3-methylamino-1-phenylpropan-1-ol
benzene
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid | 83% |
3,3-diphenylpropanoic acid N-methylamide
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether for 4h; | 66% |
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
With hydrogenchloride; aq. NaOH In methanol |
benzyl-methyl-amine
N-methyl-3,3-diphenylpropylamine
Cinnamic acid
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: thionyl chloride / Heating 2: 1,4-dioxane / 0.17 h / 20 °C 3: trifluorormethanesulfonic acid / 2 h / 20 °C 4: lithium aluminium tetrahydride / diethyl ether / 4 h View Scheme |
cinnamoyl chloride
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1,4-dioxane / 0.17 h / 20 °C 2: trifluorormethanesulfonic acid / 2 h / 20 °C 3: lithium aluminium tetrahydride / diethyl ether / 4 h View Scheme |
4-methylcinnamoyl chloride
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1,4-dioxane / 0.17 h / 20 °C 2: trifluorormethanesulfonic acid / 1 h / 20 °C 3: lithium aluminium tetrahydride / diethyl ether / 4 h View Scheme |
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1,4-dioxane / 0.17 h / 20 °C 2: trifluorormethanesulfonic acid / 1 h / 20 °C 3: lithium aluminium tetrahydride / diethyl ether / 4 h View Scheme |
4-methylcinnamic acid
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: thionyl chloride / Heating 2: 1,4-dioxane / 0.17 h / 20 °C 3: trifluorormethanesulfonic acid / 1 h / 20 °C 4: lithium aluminium tetrahydride / diethyl ether / 4 h View Scheme |
3-(3,4-Dimethylphenyl)-propensaeure
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: thionyl chloride / Heating 2: 1,4-dioxane / 0.17 h / 20 °C 3: trifluorormethanesulfonic acid / 1 h / 20 °C 4: lithium aluminium tetrahydride / diethyl ether / 4 h View Scheme |
N-methylcinnamamide
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: trifluorormethanesulfonic acid / 2 h / 20 °C 2: lithium aluminium tetrahydride / diethyl ether / 4 h View Scheme |
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: trifluorormethanesulfonic acid / 1 h / 20 °C 2: lithium aluminium tetrahydride / diethyl ether / 4 h View Scheme |
N-methyl-3,3-diphenylpropylamine
methyl vinyl ketone
4-[N-(3,3-diphenylpropyl)-N-methylamino]-2-butanone
Conditions | Yield |
---|---|
In diethyl ether at -5 - 3℃; | 90% |
N-methyl-3,3-diphenylpropylamine
2,6-dimethyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-β-chloroethyl ester 5-isopropyl ester
Conditions | Yield |
---|---|
Heating; | 85% |
3-chloro-2-methylpropan-2-ol
N-methyl-3,3-diphenylpropylamine
2,N-dimethyl-N-(3,3-diphenylpropyl)-1-amino-2-propanol
Conditions | Yield |
---|---|
In xylene for 8.5h; Heating; | 80% |
N-methyl-3,3-diphenylpropylamine
methyloxirane
1-[N-(3,3-diphenylpropyl)-N-methylamino]-2-propanol
Conditions | Yield |
---|---|
In methanol at 15 - 20℃; for 96h; | 70% |
N-methyl-3,3-diphenylpropylamine
2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-(2-chloro-ethyl) ester 5-(2-propoxy-ethyl) ester
Conditions | Yield |
---|---|
Heating; | 59% |
N-methyl-3,3-diphenylpropylamine
2-chloroethyl 2,6-dimethyl-4-(3-nitrophenyl)-5-ethoxy-carbonyl-1,4-dihydropyridine-3-carboxylate
Conditions | Yield |
---|---|
Heating; | 55% |
N-methyl-3,3-diphenylpropylamine
3-(3-chloropropyl)-1,3-dihydro-7,8-dimethoxy-2H-3-benzazepine-2-one
Conditions | Yield |
---|---|
In toluene for 10h; Heating; | 50% |
N-methyl-3,3-diphenylpropylamine
2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-(2-chloro-ethyl) ester 5-isobutyl ester
Conditions | Yield |
---|---|
Heating; | 50% |
N-methyl-3,3-diphenylpropylamine
4-Nitrophenyl chloroformate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 2h; Inert atmosphere; | 49% |
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 20℃; for 504000h; Condensation; | 36% |
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Heating; | 35% |
N-methyl-3,3-diphenylpropylamine
2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid methyl ester 3-chloropropyl ester
Conditions | Yield |
---|---|
Heating; | 35% |
N-methyl-3,3-diphenylpropylamine
4-(2,3-Dichloro-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-(2-chloro-1-methyl-ethyl) ester 5-isobutyl ester
Conditions | Yield |
---|---|
Heating; | 5% |
(6-bromo-hexyl)-diethyl-amine
N-methyl-3,3-diphenylpropylamine
N-(3,3-Diphenyl-propyl)-N',N'-diethyl-N-methyl-hexane-1,6-diamine
Conditions | Yield |
---|---|
With sodium carbonate In ethanol |
5-bromopentan-1-nitrile
N-methyl-3,3-diphenylpropylamine
5-[(3,3-Diphenyl-propyl)-methyl-amino]-pentanenitrile
Conditions | Yield |
---|---|
With sodium carbonate In ethanol |
N-methyl-3,3-diphenylpropylamine
2,6-dimethyl-4-(2,3-dichlorophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid methyl ester 2-chloroethyl ester
Conditions | Yield |
---|---|
Heating; Yield given; |
N-methyl-3,3-diphenylpropylamine
2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-(2-chloroethyl)ester-5-methyl ester
Conditions | Yield |
---|---|
Heating; Yield given; |
N-methyl-3,3-diphenylpropylamine
4-Benzo[1,2,5]oxadiazol-4-yl-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-(2-chloro-ethyl) ester 5-methyl ester
Conditions | Yield |
---|---|
Heating; Yield given; |
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 16h; Ambient temperature; Yield given; |
N-methyl-3,3-diphenylpropylamine
2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-(2-chloroethyl)ester-5-methyl ester
Conditions | Yield |
---|---|
Heating; Yield given; |
N-methyl-3,3-diphenylpropylamine
2-chloro-6,7-dimethoxyquinazolin-4-amine
Conditions | Yield |
---|---|
In i-Amyl alcohol for 5h; Heating; |
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 36 percent / K2CO3 / acetone / 504000 h / 20 °C 2: aq. NaOH / ethanol / 20 °C View Scheme |
N-methyl-3,3-diphenylpropylamine
lercanidipine
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 80 percent / xylene / 8.5 h / Heating 2: 72 percent / toluene / 2 h / 80 °C 3: 91 percent / HCl / CHCl3 / 15 °C 4: propan-2-ol / Heating View Scheme | |
Multi-step reaction with 2 steps 1: 80 percent / xylene / 8.5 h / Heating 2: dimethylformamide; CH2Cl2 / 3 h / 0 °C View Scheme |
N-methyl-3,3-diphenylpropylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 90 percent / diethyl ether / -5 - 3 °C 2: 83 percent / NaBH4 / methanol / 0.08 h / 0 °C View Scheme |
N-methyl-3,3-diphenylpropylamine
1,1,N-trimethyl-N-(3,3-diphenylpropy)-2-aminoethyl acetoacetate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 80 percent / xylene / 8.5 h / Heating 2: 72 percent / toluene / 2 h / 80 °C View Scheme |
N-methyl-3,3-diphenylpropylamine
3-Oxo-butyric acid 2-[(3,3-diphenyl-propyl)-methyl-amino]-1-methyl-ethyl ester
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 70 percent / methanol / 96 h / 15 - 20 °C 2: 68 percent / toluene / 95 °C View Scheme |
N-methyl-3,3-diphenylpropylamine
2-[1-(2,3-Dichloro-phenyl)-meth-(Z)-ylidene]-3-oxo-butyric acid 2-[(3,3-diphenyl-propyl)-methyl-amino]-1-methyl-ethyl ester
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 70 percent / methanol / 96 h / 15 - 20 °C 2: 68 percent / toluene / 95 °C 3: 93 percent / HCl / CHCl3 / 24 h / Ambient temperature View Scheme |
The Benzenepropanamine,N-methyl-gamma-phenyl-, with the CAS registry number 28075-29-8, is also known as N-Methyl-3,3-diphenyl-1-propanamine. Its EINECS number is 248-821-5. This chemical's molecular formula is C16H19N and formula weight is 225.33. What's more, its IUPAC name is called N-methyl-3,3-diphenylpropan-1-amine. This chemical is white crystals.
Physical properties of Benzenepropanamine,N-methyl-gamma-phenyl-: (1)ACD/LogP: 2.59; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -0.5; (4)ACD/LogD (pH 7.4): -0.2; (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: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 5; (12)Polar Surface Area: 3.24 Å2; (13)Index of Refraction: 1.554; (14)Molar Refractivity: 73.06 cm3; (15)Molar Volume: 227.9 cm3; (16)Surface Tension:37.5 dyne/cm; (17)Density: 0.988 g/cm3; (18)Flash Point: 164.5 °C; (19)Enthalpy of Vaporization: 59.16 kJ/mol; (20)Boiling Point: 347.4 °C at 760 mmHg; (21)Vapour Pressure: 5.41E-05 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES:c1ccccc1C(c2ccccc2)CCNC
(2)InChI:InChI=1/C16H19N/c1-17-13-12-16(14-8-4-2-5-9-14)15-10-6-3-7-11-15/h2-11,16-17H,12-13H2,1H3
(3)InChIKey:AKEGHAUFMKCWGX-UHFFFAOYAA
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