Grundinformationen
- Standard-SMILES
C1CN(C2CC2)CCN1- InChIKey
HNZJIWIXRPBFAN-UHFFFAOYSA-N- Summenformel
- C7H14N2
- Durchschnittliche Molmasse
- 126,2 g/mol
- Monoisotopische Masse
- 126,11569845
Namen und Bezeichner
- Bevorzugter Name
- 1-Cyclopropylpiperazine
- IUPAC
- 1-cyclopropylpiperazine
- Englischer Name
- 1-Cyclopropylpiperazine
- Summenformel
- C7H14N2
- Molmasse
- 126.2
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
20327-23-5- PubChem CID
- 4742004
- DTXSID
DTXSID20406303- EC Number
- 807-993-7
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,2
- Polarare Oberfläche (TPSA)
- 15,3 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 9
- Formalladung
- 0
- Komplexität
- 93,1
Physikochemische Eigenschaften
- Siedepunkt
- 43 °C/7mm · 43°C/7mm
- Dichte
- 0.94 · 0.94
- Brechungsindex
- 1.4804 · 1.4804
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- Aggregatzustand
- clear liquid
- pka
- 9.23 · 9.23±0.10(Predicted)
- Farbe
- Colorless to Light yellow
- InChI
- InChI=1S/C7H14N2/c1-2-7(1)9-5-3-8-4-6-9/h7-8H,1-6H2
- InChIKey
- HNZJIWIXRPBFAN-UHFFFAOYSA-N
- SMILES
- N1(C2CC2)CCNCC1
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H302 (60%): Harmful if swallowed [Warning Acute toxicity, oral]
P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P363, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 5 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Sicherheitsdaten
- ridadr
- 3267
- hs_code
- 2933599590
- hazard_code
- Xi
- hazard_class
- 8
- packing_group
- Ⅲ
Chemie und Industrie
Anwendungen
Verwenden1-cyclopropylpiperazine is a piperazine derivative known in the literature by synonyms such as N-cyclopropylpiperazine and 4-cyclopropylpiperazine. It has been used in the preparation of some tri- and tetrasubstituted ureas with histamine H3 antagonist receptor activity, 3-amido-4- anilinoquinolines series as CSF-1R kinase inhibitors, for the synthesis of cyclopropyl amines as modulators of the histamine H3 receptor, sulfonamide compounds as cysteine protease inhibitors, N-oxides as antibacterial agents and in the treatment of the disease caused by helicobacter infection[1].
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