(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. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Synthetic Route of C4H11NO
Fluorescence recognition of chiral amino alcohols by using a novel ionic liquid sensor was written by Cai, Pengfei;Wu, Datong;Zhao, Xiaoyong;Pan, Yuanjiang. And the article was included in Analyst (Cambridge, United Kingdom) in 2017.Synthetic Route of C4H11NO This article mentions the following:
A novel task-specific ionic liquid derived from L-phenylalaninol was prepared as an enantioselective fluorescent sensor for the 1st time. Fluorescent chiral ionic liquid I (FCIL1) is found to exhibit highly enantioselective fluorescence enhancements toward both aromatic and nonaromatic chiral amino alcs. When (S)-FCIL1 was treated with the enantiomers of phenylalaninol, a great fluorescence enhancement at 349 nm could be observed and the value of the enantiomeric fluorescence difference (ef) is 5.92. The chiral sensor (S)-FCIL1 exhibited an excellent enantioselective response behavior to D-phenylalaninol. Besides that, both the fluorescence intensity at 349 nm (I349) and the ratio of I349 to I282 depend linearly on the concentration of amino alcs. Both the concentration and the enantiomeric composition could be determined by using the chiral ionic liquid Differently, the sensor treated with the enantiomers of 2-amino-1-butanol showed an opposite result: the fluorescence intensity of the S-enantiomer is higher than that of the R-enantiomer. Also, the size of the substituents on the chiral carbon might be important for the enantioselective fluorescent response. In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3Synthetic Route of C4H11NO).
(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. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Synthetic Route of C4H11NO
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts