1-乙基哌啶结构式
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常用名 | 1-乙基哌啶 | 英文名 | 1-ethylpiperidine |
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CAS号 | 766-09-6 | 分子量 | 113.201 | |
密度 | 0.8±0.1 g/cm3 | 沸点 | 125.6±3.0 °C at 760 mmHg | |
分子式 | C7H15N | 熔点 | -20 °C | |
MSDS | 中文版 美版 | 闪点 | 18.9±0.0 °C | |
符号 |
GHS02, GHS07 |
信号词 | Danger |
Amino-acids and peptides. XXIV. The use of esters of 1-hydroxypiperidine and of other NN-dialkylhydroxylamines in peptide synthesis and as selective acylating agents.
J. Am. Chem. Soc. Dec , 6814-27, (1965)
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A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water.
Org. Lett. 3(8) , 1157-60, (2001) [reaction: see text]. The combination of water-soluble radical initiator 2,2'-azobis[2-(2-imidazolin-2-yl)propane] (VA-061), water-soluble chain carrier 1-ethylpiperidine hypophosphite (EPHP), and surfactant cetyltrimethylammonium bromide (CTAB) was found to ... |
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Room temperature phosphorescence of alpha-bromonaphthalene induced by cyclodextrin in the presence of hexahydropyridine or 1-ethylpiperidine and its application.
Anal. Chim. Acta 583(2) , 364-9, (2007) Two novel heterocyclic third components, hexahydropyridine (HHP) and 1-ethylpiperidine (EP) were firstly found to enhance room temperature phosphorescence (RTP) of alpha-bromonaphthalene (alpha-BrN) induced by cyclodextrin. The effects of equilibrium time for... |
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Stereoselective synthesis of tetrasubstituted (Z)-alkenes from aryl alkyl ketones utilizing the Horner-Wadsworth-Emmons reaction.
Chem. Pharm. Bull. 50(9) , 1300-2, (2002) Tetrasubstituted (Z)-alkenes were readily prepared through the Horner-Wadsworth-Emmons reactions of methyl 2-[bis(2,2,2-trifluoroethyl)phosphono]propionate with aryl alkyl ketones by employing Sn(OSO(2)CF(3))(2) and N-ethylpiperidine. |
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Laurence Miesch, et al
Synthesis 1 , 161-167, (2011)
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Mankil Jung and Marvin J. Miller
Tetrahedron Lett. 26 , 977-980, (1985)
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Yoshimitsu Nagao, et al
J. Am. Chem. Soc. 20 , 1418-19, (1985)
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Yoo Tanabe and Teruaki Mukaiyama
Chem. Lett. 11 , 1813-16, (1986)
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