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(1,2-diphenyl-ethyl)-carbamic acid tert-butyl ester
(R,S)-1,2-diphenylethylamine
Conditions | Yield |
---|---|
With water; sodium t-butanolate In tetrahydrofuran Heating; | 100% |
(E)-1,2-diphenyl-ethene
(R,S)-1,2-diphenylethylamine
Conditions | Yield |
---|---|
With 10-phenyl-9-(2,4,6-trimethylphenyl)acridinium tetrafluoroborate; ammonium carbonate; 2-amino-benzenethiol In dichloromethane; chlorobenzene at 20℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; Irradiation; | 98% |
Multi-step reaction with 2 steps 1: PrPPTNO / acetonitrile / 16 h / 30 °C / Irradiation 2: hydrogen; palladium on activated charcoal / ethyl acetate / 3 h / 50 °C View Scheme |
phenyl benzyl ketone
(R,S)-1,2-diphenylethylamine
Conditions | Yield |
---|---|
With ammonia; hydrogen In water at 130℃; for 24h; Autoclave; | 93% |
With ammonium formate; C25H29ClIrN2O3P at 50℃; for 18h; Leukardt-Wallach Amination; Sealed tube; | 69% |
With formic acid; ammonium carbonate | |
Stage #1: phenyl benzyl ketone With ammonium formate at 160℃; Stage #2: With hydrogenchloride In methanol | |
Multi-step reaction with 2 steps 1: hydroxylamine hydrochloride; sodium acetate / ethanol / 6 h / 60 °C 2: hydrogenchloride; palladium 10% on activated carbon; hydrogen / ethanol; water View Scheme |
cis-stilben
(R,S)-1,2-diphenylethylamine
Conditions | Yield |
---|---|
With 10-phenyl-9-(2,4,6-trimethylphenyl)acridinium tetrafluoroborate; ammonium carbonate; 2-amino-benzenethiol In dichloromethane; chlorobenzene at 20℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; Irradiation; | 93% |
Conditions | Yield |
---|---|
With sodium hexamethyldisilazane; caesium carbonate at 110℃; for 12h; Catalytic behavior; Reagent/catalyst; Sealed tube; Inert atmosphere; chemoselective reaction; | 90% |
stilbene
(R,S)-1,2-diphenylethylamine
Conditions | Yield |
---|---|
With terephthalonitrile; ammonia In water; acetonitrile; benzene for 31h; Ambient temperature; Irradiation; | 88% |
With terephthalonitrile; ammonia In water; acetonitrile for 20h; Mechanism; Ambient temperature; Irradiation; other solvent; regiochemistry on photoamination of other 1,2-diarylethene via electron transfer; | 46% |
(R,S)-1,2-diphenylethylamine
Conditions | Yield |
---|---|
With trifluoroacetic acid at 50℃; for 12.5h; | 88% |
N-(1,2-diphenyl-ethyl)-N-benzylamine
(R,S)-1,2-diphenylethylamine
Conditions | Yield |
---|---|
With palladium on activated charcoal; hydrogen In ethyl acetate at 50℃; for 3h; | 84% |
α-benzylideneamino-α-phenylacetamide
benzyl bromide
A
2-oxo-2-phenylacetamide
B
(R,S)-1,2-diphenylethylamine
C
2-Amino-2,3-diphenyl-propionamide
Conditions | Yield |
---|---|
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane Ambient temperature; phase-transfer conditions; Yields of byproduct given; | A n/a B n/a C 79% |
Conditions | Yield |
---|---|
Stage #1: phenylmagnesium bromide; benzonitrile In tetrahydrofuran; diethyl ether at 100℃; for 0.166667h; Microwave irradiation; Stage #2: With sodium tetrahydroborate In tetrahydrofuran; methanol; diethyl ether for 0.0833333h; | 76% |
This chemical is called 1,2-Diphenylethylamine, and it can also be named as Benzeneethanamine, α-phenyl-. With the molecular formula of C14H15N, its molecular weight is 197.28. The CAS registry number of this chemical is 25611-78-3, and its product categories are Amines; C11 to C38; Nitrogen Compounds.
Other characteristics of the 1,2-Diphenylethylamine can be summarised as followings: (1)ACD/LogP: 3.13; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.07; (4)ACD/LogD (pH 7.4): 0.96; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1.04; (8)ACD/KOC (pH 7.4): 8.13; (9)#H bond acceptors: 1; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 4; (12)Polar Surface Area: 3.24 Å2; (13)Index of Refraction: 1.596; (14)Molar Refractivity: 63.82 cm3; (15)Molar Volume: 187.3 cm3; (16)Polarizability: 25.3×10-24cm3; (17)Surface Tension: 44.4 dyne/cm; (18)Density: 1.02 g/cm3; (19)Flash Point: 136.8 °C; (20)Enthalpy of Vaporization: 55.2 kJ/mol; (21)Boiling Point: 311.1 °C at 760 mmHg; (22)Vapour Pressure: 0.000575 mmHg at 25°C.
Uses of this chemical: The N-bibenzyl-a-yl-benzamide could be obtained by the reactants of benzoyl chloride and 1,2-Diphenylethylamine, the reagent of 15percent sodium hydroxide and the solvent of H2O. This reaction should be taken for 1 hour at the temperature of 0 °C, and its yield is 98 %.
When you are using this chemical, please be cautious about it as the following: This chemical is irritating to eyes, respiratory system and skin, so you should wear suitable protective clothing when you use it. In case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
1.SMILES: NC(c1ccccc1)Cc2ccccc2
2.InChI: InChI=1/C14H15N/c15-14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10,14H,11,15H2
3.InChIKey: DTGGNTMERRTPLR-UHFFFAOYAN
4.Std. InChI: InChI=1S/C14H15N/c15-14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10,14H,11,15H2
5.Std. InChIKey: DTGGNTMERRTPLR-UHFFFAOYSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 145mg/kg (145mg/kg) | BEHAVIORAL: FOOD INTAKE (ANIMAL) BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) | Arzneimittel-Forschung. Drug Research. Vol. 28, Pg. 1561, 1978. Link to PubMed |
rat | LDLo | intraperitoneal | 100mg/kg (100mg/kg) | Pharmaceutical Bulletin. Vol. 1, Pg. 174, 1953. |