| Weight | 200.33 g/mol |
|---|---|
| Formula | C10H24N4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
7209-38-3 (7209-38-3)
1,4-bis(3-aminopropyl)piperazine
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- Synthesis and in vitro and in vivo antimalarial activity of N1-(7-chloro-4-quinolyl)-1,4-bis(3-aminopropyl)piperazine derivatives. (Journal of Medicinal Chemistry, 2003)
- Trypanothione reductase inhibition/trypanocidal activity relationships in a 1,4-bis(3-aminopropyl)piperazine series (Bioorganic & Medicinal Chemistry, 2000)
- Synthesis and antimalarial evaluation of new N1-(7-chloro-4-quinolyl)-1,4-bis(3-aminopropyl)piperazine derivatives (Bioorganic & Medicinal Chemistry Letters, 2005)
- Synthesis, structure and magnetic properties of a trinuclear cyano-bridged complex [Cu(bappz)(-NC)Ni(CN)2(-CN)Cu(bappz)](ClO4)2 {bappz=1,4-bis(3-aminopropyl)piperazine} (Inorganic Chemistry Communications, 2003)
- Synthesis, Characterization anc Dopamine Selectivity of 1,4-bis(3-aminopropyl)piperazine - Containing Polyimide (Polymer Bulletin, 2004)
- Synthesis, characterization, and properties of organically templated lanthanide oxalatophosphates with a three-dimensional honeycomb structure: (H4APPIP)[Ln3(C2O4)(5.5)(H2PO4)2].5H2O (Ln = Er-Lu, APPIP = 1,4-bis(3-aminopropyl)piperazine). (Inorganic Chemistry, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,4-bis(3-aminopropyl)piperazine
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SMILESC1CN(CCN1CCCN)CCCN
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InChIKeyXUSNPFGLKGCWGN-UHFFFAOYSA-N
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