Weight | 190.29 g/mol |
---|---|
Formula | C12H18N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
1-(1-Phenylethyl)piperazine (69628-75-7)
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- Enantiomeric resolution of 1-[2-(3-hydroxyphenyl)-1-phenylethyl]-4-(3-methyl-2-butenyl)piperazine by reversed-phase high-performance liquid chromatography using a chiral mobile phase (Journal of Chromatography A, 1983)
- 2,5-diphenyl-1,4-(trifluoromethylsulfonyl)piperazine from N-(2-bromo-2-phenylethyl)trifluoromethanesulfonamide (Russian Journal of Organic Chemistry, 2010)
- Analgesic and other pharmacological activities of a new narcotic antagonist analgesic ()1(3methyl2butenyl)4[2(3hydroxyphenyl)1phenylethyl]piperazine and its enantiomorph in experimental animals (Journal of Pharmacy and Pharmacology, 1980)
- 1- (2-m- methanesulfonamide phenylethyl)-4-(m-trifluoromethylphenyl) piperazine and pharmaceutically acceptable salts and solvates thereof (2001)
- ChemInform Abstract: 2,5Diphenyl1,4(trifluoromethylsulfonyl)piperazine (III) from N(2bromo2phenylethyl)trifluoromethanesulfonamide (II). (ChemInform, 2011)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C1=CC=CC=C1)N2CCNCC2
-
InChIKeyPYBNQKSXWAIBKN-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Reactant
+
N'-(1-phenylethyl)ethane-1,2-diamine
(Reductive amination)
benzene
+
Reactant
(Friedel-Crafts alkylation)
Reactant
+
Piperazine
(Chan-Lam coupling reaction)
Similar Compounds
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1-benzyl-1,4-diazepan-5-one
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1-Benzhydrylpiperazine
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N-benzyl-2-chloro-N-(2-chloroethyl)ethanamine
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101-32-6
(101-32-6)
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[2-(piperazin-1-ylmethyl)phenyl]methanol
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