(1S, 2S) -2-(2-isopropoxyethylamino) cyclopentanol hydrochloride CAS: 1599293-28-3 199293-70-9

((1S,2S)-2-(2-isopropoxyethylamino)cyclopentanol hydrochloride muaj kev cia siab hauv kev kho mob tshuaj ua ib qho nruab nrab rau kev tsim cov tshuaj muaj peev xwm tsom mus rau cov hom phiaj tshwj xeeb lossis cov kab mob. Cov kws tshawb fawb tuaj yeem tshawb nrhiav nws cov khoom pharmacological los ntawm kev ntsuam xyuas nws cov enantiomeric purity thiab kawm nws cov kev sib cuam tshuam nrog cov kab mob biological los ntsuam xyuas nws cov peev xwm kho mob. Lub compound's chiral xwm yuav raug siv los tsim cov neeg sawv cev tshuaj xaiv nrog kev ua haujlwm zoo dua thiab txo cov teebmeem tsis zoo. Hauv kev tsim cov organic, cov tshuaj no ua haujlwm ua tus thawj coj tseem ceeb rau kev nkag mus rau cov qauv sib txawv los ntawm kev hloov pauv pab pawg ua haujlwm lossis cov tshuaj derivatization. Nws kev koom ua ke rau hauv cov txheej txheem tsim tso cai rau kev tsim cov qauv molecular nyuaj rau kev kawm txog kev sib raug zoo ntawm cov qauv-kev ua ub no, tsim cov ntaub ntawv tshiab, lossis tshawb nrhiav asymmetric catalysis. Los ntawm kev siv nws cov stereochemistry thiab reactivity, cov kws tshawb fawb tuaj yeem txhim kho cov txheej txheem tsim thiab tsim cov tshuaj tshiab rau kev siv kev tshawb fawb thiab kev lag luam. Zuag qhia tag nrho, ((1S,2S)-2-(2-isopropoxyethylamino)cyclopentanol hydrochloride qhia txog kev ua tau zoo thiab muaj peev xwm hauv kev tshawb pom tshuaj, organic synthesis, thiab kev tsim kho tshiab tshuaj, qhia txog nws qhov tseem ceeb hauv kev txhim kho kev paub txog kev tshawb fawb thiab tshuaj. kev nce qib.