| Identification | More | [Name]
1,2-DIPHENYLETHYLAMINE | [CAS]
25611-78-3 | [Synonyms]
AKOS BC-0994
TIMTEC-BB SBB000367
α-Benzylbenzylamine
1,2-DIPHENYLETHYLAMI
1,2-Diphenylethanamine
α-Phenylphenethylamine
1,2-DIPHENYLETHYLAMINE
ALPHA-BENZYLBENZYLAMINE
α-Phenylbenzeneethanamine
1,2-DIPHENYLETHAN-1-AMINE
1,2-Diphenylethylamine 97%
alpha-phenyl-phenethylamin
alpha-Phenylphenethylamine
1-AMINO-1,2-DIPHENYLETHANE
1,2-Diphenylethylamine >
1,2-DIPHENYLETHYLAMINE 97+%
Benzeneethanamine, α-phenyl-
Phenethylamine, alpha-phenyl-
alpha,beta-diphenylethylamine
alpha-phenylbenzeneethanamine
1-AMINO-1,2-DIPHENYLETHANE 97%
1,2-DIPHENYL-ETHANE-1,2-DIAMINE
Benzeneethanamine, alpha-phenyl-
1-Amino-1,2-diphenylethane
alpha-Benzylbenzylamine | [EINECS(EC#)]
247-126-4 | [Molecular Formula]
C14H15N | [MDL Number]
MFCD00008063 | [Molecular Weight]
197.28 | [MOL File]
25611-78-3.mol |
| Chemical Properties | Back Directory | [Boiling point ]
310-311 °C750 mm Hg(lit.) | [density ]
1.02 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.58(lit.)
| [Fp ]
>230 °F
| [form ]
liquid | [pka]
8.78±0.10(Predicted) | [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 | [InChIKey]
DTGGNTMERRTPLR-UHFFFAOYSA-N | [SMILES]
NC(Cc1ccccc1)c2ccccc2 | [CAS DataBase Reference]
25611-78-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN2735 | [WGK Germany ]
3
| [RTECS ]
SI2299000
| [HazardClass ]
8 | [HS Code ]
2921490090 | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Uses]
1,2-Diphenylethylamine (cas# 25611-78-3) is used in the preparation of GDP-triazoles for inhibition of human α-1,3-fucosyltransferases. | [General Description]
(S)- and (R)-enantiomers of 1,2-diphenylethylamine are the precursors for synthesis of (S)- and (R)-1-(1,2-diphenylethyl)piperidine. |
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