![]() 4-哌啶甲醇结构式
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常用名 | 4-哌啶甲醇 | 英文名 | 4-Piperidinemethanol |
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CAS号 | 6457-49-4 | 分子量 | 115.174 | |
密度 | 1.0±0.1 g/cm3 | 沸点 | 198.2±13.0 °C at 760 mmHg | |
分子式 | C6H13NO | 熔点 | 55-59 °C(lit.) | |
MSDS | 中文版 美版 | 闪点 | 92.3±10.5 °C | |
符号 |
![]() GHS05 |
信号词 | Danger |
Expedient protocol for solid-phase synthesis of secondary and tertiary amines.
Org. Lett. 6 , 1935-1938, (2004) [reaction: see text] An expedient solid-phase synthetic approach to secondary and tertiary amines was developed. The protocol employs conversion of resin-bound amino alcohols to the corresponding iodides, followed by iodide displacement with primary or second... |
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Synthesis and characterization of a triazine dendrimer that sequesters iron(III) using 12 desferrioxamine B groups.
Bioorg. Med. Chem. 18(15) , 5749-53, (2010) The synthesis of a third generation triazine dendrimer, 1, containing multiple, iron-sequestering desferrioxamine B (DFO) groups is described. Benzoylation of the hydroxamic acid groups of DFO and formation of a reactive dichlorotriazine provide the intermedi... |
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Synthesis and structure-activity relationships of 2-phenyl-1-[(pyridinyl- and piperidinylmethyl)amino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents.
Bioorg. Med. Chem. Lett. 19(2) , 301-4, (2009) Continuous efforts on the synthesis and structure-activity relationships (SARs) studies of modified 1-benzylamino-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents, allowed identification of new 1-[(pyridinyl- and piperidinylmethyl)amino] de... |
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Standard molar enthalpies of formation of 2-, 3-, and 4-piperidinomethanol isomers. da Silva MAVR and Cabral JITA
J. Chem. Thermodyn. 38(8) , 1008-1012, (2006)
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Enzymatic synthesis, thermal and crystalline properties of a poly (β-amino ester) and poly (lactone-co-β-amino ester) copolymers. Martino L, et al.
Polymer 53(9) , 1839-1848, (2012)
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Synthesis, spectroscopy, and biological activity of heterobimetallic complexes containing Sn (IV) and Pd (II) with 4-(hydroxymethyl) piperidine-1-carbodithioic acid. Anwar MT, et al.
Russ. J. Gen. Chem. 83(12) , 2380-2385, (2013)
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Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as factor Xa inhibitor. Nishida H, et al.
Chem. Pharm. Bull. 49(10) , 1237-1244, (2001)
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