| Weight | 186.255 g/mol |
|---|---|
| Formula | C9H18N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1-Boc-piperazine (57260-71-6)
tert-butyl piperazine-1-carboxylate · 57260-71-6
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- Efficient copper-catalyzed cross-coupling of 1-Boc-piperazine with aryl iodides and its application in the synthesis of trazodone (Tetrahedron Letters, 2013)
- Synthesis, Characterization, X-ray Diffraction Studies, and Biological Evaluation of Tert-butyl 4-(5-(3-fluorophenyl)-1,2,4-oxadiazol-3-yl) piperazine-1-carboxylate (Molecular Crystals and Liquid Crystals, 2015)
- Synthesis and Molecular Structure of tert-Butyl 4-(2-tert-butoxy-2-oxoethyl)piperazine-1-carboxylate (2012)
- Synthesis, characterization, X-ray diffraction studies and biological evaluation of tert-butyl 4-(2-ethoxy-2-oxoethyl)-piperazine-1-carboxylate and tert-butyl 4-(2-hydrazino-2-oxoethyl)piperazine-1-carboxylate (Research on Chemical Intermediates, 2016)
- Crystal structure of tert-butyl (Z)-4-(2-(5-methoxy-3-(2-((methylthio)carbonothioyl)hydrazono)-2-oxoindolin-1-yl)ethyl)piperazine-1-carboxylate, C22H31N5O4S2 (Zeitschrift Fur Kristallographie-new Crystal Structures, 2017)
- ChemInform Abstract: Efficient CopperCatalyzed CrossCoupling of 1Bocpiperazine with Aryl Iodides and Its Application in the Synthesis of Trazodone. (ChemInform, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - tert-butyl piperazine-1-carboxylate
- 57260-71-6
-
SMILESCC(C)(C)OC(=O)N1CCNCC1
-
InChIKeyCWXPZXBSDSIRCS-UHFFFAOYSA-N
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Most-cited Publications
Safety
Alternate Names
Estimated Properties
| Boiling Point | 251.72 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 256.72 C | EPI Suite |
| Density | 1.06 g/cm3 | EPA T.E.S.T. |
| Flash Point | 120.81 C | EPA T.E.S.T. |
| Melting Point | 65.07 C | EPI Suite |
| Water Solubility | 38409.4 mg/L | EPA T.E.S.T. |
| Water Solubility | 472020 mg/L | EPI Suite |
External Links
Synthesis
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1-Boc-piperazine
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