(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Name: (R)-2-Aminobutan-1-ol
Chiral Imidazolium-Functionalized Au Nanoparticles: Reversible Aggregation and Molecular Recognition was written by Lomeli-Rosales, Diego Alberto;Rangel-Salas, Irma Idalia;Zamudio-Ojeda, Adalberto;Carbajal-Arizaga, Gregorio Guadalupe;Godoy-Alcantar, Carolina;Manriquez-Gonzalez, Ricardo;Alvarado-Rodriguez, Jose Guadalupe;Martinez-Otero, Diego;Cortes-Llamas, Sara Angelica. And the article was included in ACS Omega in 2016.Name: (R)-2-Aminobutan-1-ol This article mentions the following:
Gold nanoparticles (AuNPs) stabilized by imidazolium salts derived from amino acids [glycine (1), rac-alanine (2), L-phenylalanine (3), and rac-methionine (4)] were prepared The AuNPs were stabilized the most by 4, which kept the particles dispersed in water for months at pH > 5.5. These AuNPs exhibited a well-defined absorption band at 517 nm and had an average particle size of 11.21 ± 0.07 nm. The 4-AuNPs were reversibly aggregated by controlling the pH of the solution Chiral R,R-4-AuNPs and S,S-4-AuNPs were synthesized, and the chiral environment on the nanoparticle surface was confirmed using CD; these nanoparticles exhibited a mol. recognition of chiral substrates. Furthermore, they showed potential for separating racemic mixtures when supported on a layered double hydroxide. In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3Name: (R)-2-Aminobutan-1-ol).
(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Name: (R)-2-Aminobutan-1-ol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts