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检测方案
95%
形式
solid
mp
53-56 °C (lit.)
SMILES字符串
C1CCN(C1)C2CCNCC2
InChI
1S/C9H18N2/c1-2-8-11(7-1)9-3-5-10-6-4-9/h9-10H,1-8H2
InChI key
STWODXDTKGTVCJ-UHFFFAOYSA-N
一般描述
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.
应用
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:
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警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
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)
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
Theoretical and experimental vibrational spectroscopic study of 4-(1-Pyrrolidinyl) piperidine.
Parlak C.
Journal of Molecular Structure, 966(1), 1-7 (2010)
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