Merck
CN

392243

Sigma-Aldrich

1-甲醛哌嗪

technical grade, 85%

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别名:
1-哌嗪甲醛
Empirical Formula (Hill Notation):
C5H10N2O
CAS号:
分子量:
114.15
Beilstein:
110295
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

等级

technical grade

检测方案

85%

形式

liquid

密度

1.107 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)N1CCNCC1

InChI

1S/C5H10N2O/c8-5-7-3-1-6-2-4-7/h5-6H,1-4H2

InChI key

MSSDTZLYNMFTKN-UHFFFAOYSA-N

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一般描述

1-Formylpiperazine, a secondary alicyclic amine is a piperazine derivative. Its synthesis has been reported. The kinetics of its reaction with O-aryl S-aryl dithiocarbonates has been studied. The IR and Raman spectra of 1-formylpiperazine have been investigated.

应用

1-Formylpiperazine is sutable for use as a test compound in the kinetic study of the reaction of 4-nitrophenyl 2-thiophenecarboxylate with secondary alicyclic amines.

法规信息

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Kinetics and mechanism for the reaction of 4-nitrophenyl 2-thiophenecarboxylate with secondary alicyclic amines.
Um IH, et al.
Bull. Korean Chem. Soc., 23(3), 381-384 (2002)
Reactions of O-aryl S-aryl dithiocarbonates with secondary alicyclic amines in aqueous ethanol. Kinetics and mechanism.
Castro EA, et al.
Journal of Physical Organic Chemistry, 24(6), 466-473 (2011)
1-Formylpiperazine and related compounds.
Horrom BW, et al.
Journal of the American Chemical Society, 77(3), 753-754 (1955)
Gürkan Keşan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 118, 1113-1120 (2013-10-29)
Infrared and Raman spectra of 1-formylpiperazine (1-fp) have been recorded in the region of 4000-50 cm(-1). The conformational analysis, optimized geometric parameters, normal mode frequencies and corresponding vibrational assignments of 1-fp (C5H10N2O) have been examined by means of Becke-3-Lee-Yang-Parr (B3LYP)
Gu-cai Li et al.
Die Pharmazie, 70(8), 511-514 (2015-09-19)
Five indolin-2-one derivatives bearing piperazinylbutyl side chains attached to the amide nitrogen were synthesized from 2-indolinone. 1-(4-Bromobutyl)-indolin-2-one was reacted with 1-piperazinecarboxaldehyde to form 1-(4-(4-formyl-1-piperazinyl)butyl)indolin-2-one (2). In the presence of H2SO4, the aldehyde moiety was removed from 1-(4-(4-formyl-1-piperazinyl)butyl)indolin-2-one and then 1-(4-(1-piperazinyl)butyl)indolin-2-one

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