Detail of "5452-83-5"
- CAS Number:
- 5452-83-5
- Name:
Pyridine,2-[2-(1-piperidinyl)ethyl]-
- Molecular Structure:
![Molecular Structure of 5452-83-5 (Pyridine,2-[2-(1-piperidinyl)ethyl]-)](http://www.lookchem.com/300w/2010/0622/5452-83-5.jpg)
- Formula:
- C12H18 N2
- Molecular Weight:
- 190.28
- Synonyms:
- Piperidine,1-[2-(2-pyridyl)ethyl]- (6CI,7CI,8CI); 2-(2-Piperidinoethyl)pyridine; NSC 18995
- Density:
- 1.006g/cm3
- Boiling Point:
- 272.3°Cat760mmHg
- Flash Point:
- 123.1°C
Pyridine,2-[2-(1-piperidinyl)ethyl]-
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Reference
- The mass spectra of some 2- and 4-pyridylethylamines
- The mass spectra of some 2- and 4-pyridylethylamines.There are some reagents like 5452-83-5 is used in this study. Czuba, W.; Rutkowski, K.; Kowalski, P. (Inst. Org. Chem. Technol., Tech.There are some reagents like 5452-83-5 is used in this study. Univ., Krakow, Pol.). Org. Mass Spectrom., 13(4), 203-6 (English) 1978. CODEN: ORMSBG. ISSN: 0030-493X. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The mass spectra of 19 N,N-disubstituted (2-aminoethyl)pyridines are reported and their main fragmentation paths analyzed. Both a- and b-cleavage occur, but b-cleavage predominates. The occurrence of a-cleavage was shown by the presence of [vinylpyridine]·+ and [ethylenepyridine]·+ ions and by further fragmentation of [R2NH]·+ ion radicals. Pyrroloethyl- and [(ethylphenylamino)ethyl]pyridines are more stable than N,N-dialkylaminoethyl-, pyrrolidinoethyl-, piperidinoethyl- and morpholinoethylpyridines. ..
- The mass spectra of some 2- and 4-pyridylethylamines
- The mass spectra of some 2- and 4-pyridylethylamines.There are some reagents like 5452-83-5 is used in this study. Czuba, W.; Rutkowski, K.; Kowalski, P. (Inst. Org. Chem. Technol., Tech.There are some reagents like 5452-83-5 is used in this study. Univ., Krakow, Pol.). Org. Mass Spectrom., 13(4), 203-6 (English) 1978. CODEN: ORMSBG. ISSN: 0030-493X. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The mass spectra of 19 N,N-disubstituted (2-aminoethyl)pyridines are reported and their main fragmentation paths analyzed. Both a- and b-cleavage occur, but b-cleavage predominates. The occurrence of a-cleavage was shown by the presence of [vinylpyridine]·+ and [ethylenepyridine]·+ ions and by further fragmentation of [R2NH]·+ ion radicals. Pyrroloethyl- and [(ethylphenylamino)ethyl]pyridines are more stable than N,N-dialkylaminoethyl-, pyrrolidinoethyl-, piperidinoethyl- and morpholinoethylpyridines. ..