Gisbert, Yohan et al. published their research in Chemistry – A European Journal in 2021 | CAS: 41191-92-8

Ethyl 3-amino-4-methylbenzoate (cas: 41191-92-8) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Related Products of 41191-92-8

Divergent Synthesis of Molecular Winch Prototypes was written by Gisbert, Yohan;Abid, Seifallah;Kammerer, Claire;Rapenne, Gwenael. And the article was included in Chemistry – A European Journal in 2021.Related Products of 41191-92-8 This article mentions the following:

We report the synthesis of conceptually new prototypes of mol. winches [(η5-R4C5-bp-XTrzR1)(Ind3BH)Ru] [R = 4-FcC6H4; bp = 1,1′-biphenyl-4,4′-diyl; X = CH2NHCOCH2CH2(OCH2CH2)8; Trz = 1,2,3-triazole-1,4-diyl; R1 = 9-triptycenyl (tpc), CH2CH2OCOC(C60)CO2Et, 3,5-C6H3(CC-9-tpc)2, 10,20-(CCtpc)2Por-Zn] with the ultimate aim to investigate the work performed by a single ruthenium-based mol. motor anchored on a surface by probing its ability to pull a load upon elec.-driven directional rotation. According to a technomimetic design, the motor was embedded in a winch structure, with a long flexible polyethylene glycol chain terminated by an azide hook to connect a variety of mol. loads. The structure of the motor was first derivatized by means of two sequential cross-coupling reactions involving a penta(4-halogenophenyl)cyclopentadienyl hydrotris(indazolyl)borate ruthenium(II) precursor and the resulting benzylamine derivative was next exploited as key intermediate in the divergent synthesis of a family of nanowinch prototypes. A one-pot method involving sequential peptide coupling and Cu-catalyzed azide-alkyne cycloaddition was developed to yield four loaded nanowinches, with load fragments encompassing triptycene, fullerene and porphyrin moieties. In the experiment, the researchers used many compounds, for example, Ethyl 3-amino-4-methylbenzoate (cas: 41191-92-8Related Products of 41191-92-8).

Ethyl 3-amino-4-methylbenzoate (cas: 41191-92-8) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Related Products of 41191-92-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics