437352
4-吡咯烷-1-基哌啶
95%
别名:
1-(Piperidin-4-yl)pyrrolidine
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关于此项目
经验公式（希尔记法）:
C9H18N2
化学文摘社编号:
分子量:
154.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
225-676-6
MDL number:
产品名称
4-吡咯烷-1-基哌啶, 95%
InChI key
STWODXDTKGTVCJ-UHFFFAOYSA-N
InChI
1S/C9H18N2/c1-2-8-11(7-1)9-3-5-10-6-4-9/h9-10H,1-8H2
SMILES string
C1CCN(C1)C2CCNCC2
assay
95%
form
solid
mp
53-56 °C (lit.)
Application
4-(1-Pyrrolidinyl)piperidine was employed for the synthesis of the following analogs:
- 4-pyrrolidin-1´-yl-1-[2-(2″-nitro-phenyl)-2-oxo-ethyl]-piperidinium bromide
- 4-pyrrolidin-1´-yl-1-[2-(3″-nitro-phenyl)-2-oxo-ethyl]-piperidinium bromide
- 4-pyrrolidin-1´-yl-1-[2-(2″,4″-dimethoxy-phenyl)-2-oxo-ethyl]-piperidinium bromide
- 4-pyrrolidin-1´-yl-1-[2-(3″,4″-dihydroxy-phenyl)-2-oxo-ethyl]-piperidinium bromide
Reactant for synthesis of:
Small molecule ligands of methyl-lysine binding proteins
Small molecules that restore E-cadherin expression and reduce invasion in colorectal carcinoma cells
Selective Polo-like kinase 1 inhibitors
Molecules with effects on plasma glucose levels
Vasopressin1b receptor antagonists
IKKβ inhibitors
Small molecule ligands of methyl-lysine binding proteins
Small molecules that restore E-cadherin expression and reduce invasion in colorectal carcinoma cells
Selective Polo-like kinase 1 inhibitors
Molecules with effects on plasma glucose levels
Vasopressin1b receptor antagonists
IKKβ inhibitors
General description
4-(1-Pyrrolidinyl)piperidine (4-pypp) has been reported to form Hofmann type complexes [M(4-pypp)2Ni(CN)4] (M=Ni or Co) and their FT-IR and Raman spectra have been studied. FT-IR, Raman spectra and the vibrational spectra of 4-pypp have been recorded between 4000 and 400cm-1.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Nousheen Mushtaq et al.
Pakistan journal of pharmaceutical sciences, 23(2), 220-223 (2010-04-07)
In the present study some compounds of 4-(1-Pyrrolidinyl) Piperidine (I) have been synthesized. Structures of compounds were confirmed by using HNMR, IR, Mass and UV spectrophotometer techniques. All the derivatives (II, III, IV and V) and the parent compound (I)
Theoretical and experimental vibrational spectroscopic study of 4-(1-Pyrrolidinyl) piperidine.
Parlak C.
Journal of Molecular Structure, 966(1), 1-7 (2010)
Cemal Parlak
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 99, 12-17 (2012-10-09)
Some new Hofmann type complexes with chemical formula of M(4 pypp)(2)Ni(CN)(4) (where 4 py pp=4-(1-pyrrolidinyl)piperidine and MNi or Co) were prepared and their FT-IR and Raman spectra were reported in the region of 4000-200 cm(-1) and 4000-100 cm(-1), respectively. The
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