2-Anilinoethanol structure 
             | 
        Common Name | 2-Anilinoethanol | ||
|---|---|---|---|---|
| CAS Number | 122-98-5 | Molecular Weight | 137.179 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 286.9±13.0 °C at 760 mmHg | |
| Molecular Formula | C8H11NO | Melting Point | -30 °C | |
| MSDS | Chinese USA | Flash Point | 151.4±10.5 °C | |
| Symbol | 
             
            
             
            
             
            
            GHS05, GHS06, GHS08  | 
        Signal Word | Danger | |
| 
                        
                        Effect of concentrate feeder design on performance, eating and animal behavior, welfare, ruminal health, and carcass quality in Holstein bulls fed high-concentrate diets.
                        
                        
                         J. Anim. Sci. 93 , 3018-33, (2015) A total of 240 Holstein bulls (121 ± 2.0 kg initial BW; 99 ± 1.0 d of age), from 2 consecutive fattening cycles, were randomly allocated in 1 of 6 pens and assigned to 1 of the 3 treatments consisting of different concentrate feeder designs: a control feeder ...  | 
                    |
| 
                        
                        Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation.
                        
                        
                         Chemistry 9(22) , 5567-80, (2003) Four new chiral bis(amino alcohol)oxalamides (1-4: amino alcohol=leucinol, valinol, phenylglycinol, and phenylalaninol, respectively) have been prepared as low-molecular-weight organic gelators. Their gelation properties towards various organic solvents and m...  | 
                    |
| 
                        
                        A colorimetric chiral sensor based on chiral crown ether for the recognition of the two enantiomers of primary amino alcohols and amines.
                        
                        
                         Chirality 23(4) , 349-53, (2011) A new colorimetric chiral sensor material consisting of three different functional sites such as chromophore (2,4-dinitrophenylazophenol dye), binding site (crown ether), and chiral barrier (3,3'-diphenyl-1,1'-binaphthyl group) was prepared and applied to the...  | 
                    |
| 
                        
                        Synthesis of highly enantioenriched chiral alpha-aminoorganotins via diastereoselective ring opening of chiral N-(arenesulfonyl) 2-tributylstannyloxazolidines.
                        
                        
                         J. Org. Chem. 74(16) , 5822-38, (2009) trans-N-(Arenesulfonyl)-2-tributylstannyloxazolidines derived from (R)-phenylglycinol were diastereoselectively ring-opened by soft organometallic reagents in the presence of BF(3).OEt(2). Both higher order organocuprates and allyltributyltin afforded the des...  | 
                    |
| 
                        
                        Fluorescence sensing of ammonium and organoammonium ions with tripodal oxazoline receptors.
                        
                        
                         Org. Lett. 5(9) , 1419-22, (2003) A new class of fluorescence sensors for ammonium and organoammonium ions has been disclosed. One of the sensors, an alaninol-derived tripodal oxazoline (1a) shows significant fluorescence enhancement upon binding NH(4)(+) but little response toward K(+), Na(+...  | 
                    |
| 
                        
                        Stereoselectivity in the salt-cocrystal products formed by phenylglycinol or phenylglycine with their respective sodium or hydrochloride salts.
                        
                        
                         Chirality 25(1) , 8-15, (2013) The salt and stereoselective cocrystal phenomena associated with 2-phenylglycinol and 2-phenylglycine have been studied using X-ray powder diffraction and differential scanning calorimetry. The chiral identities of the free acids and their sodium salts, or th...  | 
                    |
| 
                        
                        Enantioseparation of phenylglycinol in chiral-modified zeolite HY: a molecular simulation study.
                        
                        
                         Chirality 19(6) , 514-7, (2007) A mechanism has been proposed for the separation of valinol enantiomers using a chiral-modified zeolite HY (i.e., zeolite HY containing (+)-(1R;2R)-hydrobenzoin) Molecular modeling of chiral-modified zeolite HY employed in enantioselective separation. Jirapon...  | 
                    |
| 
                        
                        Straightforward stereoselective access to cyclic peptidomimetics.
                        
                        
                         J. Org. Chem. 74(11) , 4429-32, (2009) The preparation of cyclic dipeptide mimetics from chiral imino lactones derived from (R)-phenylglycinol is described. Key steps of the synthetic route included the fully stereoselective construction of a quaternary center, the formation of six-, seven-, or ei...  | 
                    |
| 
                        
                        Diastereoselective protonation of lactam enolates derived from (R)-phenylglycinol. A novel asymmetric route to 4-phenyl-1,2,3, 4-tetrahydroisoquinolines.
                        
                        
                         Org. Lett. 2(15) , 2185-7, (2000) Highly diastereoselective protonation of chiral lactam enolates of 4-substituted-1,4-dihydroisoquinolin-3-ones is reported. Protonation and alkylation processes of these lactam enolates derived from phenylglycinol occur with opposite diastereofacial selectivi...  | 
                    |
| 
                        
                        An (R)-specific N-methyltransferase involved in human morphine biosynthesis.
                        
                        
                         Arch. Biochem. Biophys. 506(1) , 42-7, (2011) The biosynthesis of morphine, a stereochemically complex alkaloid, has been shown to occur in plants and animals. A search in the human genome for methyltransferases capable of catalyzing the N-methylation of benzylisoquinoline alkaloids, as biosynthetic prec...  |