| Weight | 238.334 g/mol |
|---|---|
| Formula | C16H18N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
2,3-diphenylpiperazine (143699-24-5)
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- Penicillin acylase-catalyzed peptide synthesis: a chemo-enzymatic route to stereoisomers of 3,6-diphenylpiperazine-2,5-dione (Tetrahedron-asymmetry, 2000)
- A Simple Method of Synthesis of (.+.)2,3Diarylpiperazines and a Novel Method of Resolution of (.+.)2,3Diphenylpiperazine. (Journal of Organic Chemistry, 2006)
- Efficient resolution of ()-trans-2,3-diphenylpiperazine using (1S)-(+)-10-camphorsulfonic acid and enrichment of enantiomeric purity of non-racemic 2,3-diphenylpiperazine using different achiral acids (Journal of Chemical Sciences, 2008)
- The formation of 2,3-dicyano-2,3-diphenylpiperazine from 2,3-diphenyl-5,6-dihydropyrazine and hydrogen cyanide (Journal of Heterocyclic Chemistry, 1972)
- Photochamical cis, trans-Isomerization in the 2,3-Diphenylpiperazine Series (Heterocycles, 1982)
- 1,4-Diformyl-t-5-methyl-r-2,t-3-diphenylpiperazine-1,4-dicarbaldehyde (Acta Crystallographica Section C-crystal Structure Communications, 1999)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNC(C(N1)C2=CC=CC=C2)C3=CC=CC=C3
-
InChIKeyNXYCTQXWYWRZDE-UHFFFAOYSA-N
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Synthesis
benzene
+
Reactant
(Friedel-Crafts alkylation)
Reactant
+
1,2-diphenylethane-1,2-diamine
(Reductive amination)
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5424-66-8
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1-(4-bromophenyl)-N-methylpropan-1-amine
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2-(3,4-dihydroisoquinolin-2(1H)-yl)ethanamine
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66512-37-6
(66512-37-6)
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2,3-diphenylpiperazine
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