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4-哌啶甲醇

4-哌啶甲醇结构式
4-哌啶甲醇结构式
品牌特惠专场
常用名 4-哌啶甲醇 英文名 4-Piperidinemethanol
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
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...

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...

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...

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)

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)

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)

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)