72098-53-4Relevant academic research and scientific papers
METHOD FOR SYNTHESIZING AMINES
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Paragraph 0278-0280, (2021/05/28)
The invention relates to a process for preparing certain amines, wherein, in a first step, a corresponding amino alcohol is reacted with a suitable carbonyl compound and then, in a second step, the intermediate obtained in the first step is reacted with a suitable amine component to form the desired amine.
AMINE FOR RAPID-CURING EPOXY RESIN COMPOSITIONS
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Paragraph 0196-0197, (2018/04/13)
An amine of formula (I) which is particularly suitable for use as a curing agent for epoxy resins. The amine of formula (I) is devoid of non-incorporable toxic phenols, and is low-viscosity and pale in colour. It allows the production of easily-workable, low-emission or emission-free epoxy resin products which cure rapidly even at relatively low ambient temperatures thus obtaining a high degree of hardness and a nice surface with hardly any yellowing. This is particularly suited to use in floor or top coatings.
Crystal structure and interaction with bovine serum albumin of the Cu(I/II) complex [C20H32Cu2I3N 4]n
Liu, Yu-Fen,Xia, Hai-Tao,Rong, De-Fu
experimental part, p. 2919 - 2934 (2012/09/21)
[C20H32Cu2I3N4] n was synthesized and characterized by elemental analysis, ESI-MS spectrometry, and IR spectra. The crystal structure was determined by X-ray single-crystal diffraction. The
Nosylaziridines: Activated aziridine electrophiles
Maligres, Peter E.,See, Marjorie M.,Askin, David,Reider, Paul J.
, p. 5253 - 5256 (2007/10/03)
Nosylaziridines are highly reactive electrophiles towards a variety of nucleophiles yielding the corresponding SN2 adducts without competing attack on the nosyl functionality (SNAr). The resulting primary nosylamide adducts can he readily cleaved under mild conditions to provide the primary amines.
Synthesis of Isomeric N-Benzyl Derivatives of 1,2-Propanediamine
Kurganov, Alexandr,Zhuchkova, Lydmila,Davankov, Vadim
, p. 786 - 790 (2007/10/02)
Benzaldehyde reacts with the 1-amino group of 1,2-propanediamine (1) to give a Schiff base much more readily than with the 2-amino group.This difference permits synthesis of all the isomeric mono-and dibenzyl derivatives of racemic and chiral 1,2-propaned
