(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol 丨 CAS 886061-26-3

(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol feem ntau yog siv los ua chiral intermediate hauv kev sib txuas ntawm cov tshuaj, bioactive compounds, thiab tshuaj tshwj xeeb. Nws yog ib lub tsev thaiv rau kev npaj ntawm -amino cawv derivatives, uas yog ib qho tseem ceeb scaffolds nyob rau hauv tshuaj chemistry rau kev loj hlob ntawm central paj hlwb cov neeg sawv cev, enzyme inhibitors, thiab receptor modulators. Cov compound no feem ntau siv rau hauv kev tshawb nrhiav tshuaj tshawb fawb los tsim cov stereochemically txhais cov molecules nrog rau kev ua lom lom. Nws kuj yog siv nyob rau hauv cov synthesis ntawm chiral ligands thiab catalysts, qhov twg nws cov amino thiab hydroxyl pawg muab qhov chaw rau functionalization thiab derivatization. Tsis tas li ntawd, nyob rau hauv cov chaw soj ntsuam kev tshawb fawb, nws tau ua hauj lwm los kawm txog cov tshuaj tiv thaiv mechanisms, asymmetric synthesis, thiab cov qauv-kev sib raug zoo hauv kev tsim tshuaj.

Cov txiaj ntsig ntawm (S)-3-Amino-3-(4-chlorophenyl)propan-1-ol tshwm sim los ntawm nws qhov siab enantiomeric purity, ntau pab pawg, thiab tshuaj lom neeg ruaj khov. Nws S-configuration tso cai rau kev npaj ntawm optically active compounds, uas yog ib qho tseem ceeb nyob rau hauv cov tshuaj chemistry qhov twg stereochemistry muaj zog influences pharmacological kev ua si. Kev sib xyaw ua ke ntawm amino, hydroxyl, thiab chlorophenyl functionalities muab ntau yam tshuaj tiv thaiv qhov chaw, ua kom xaiv derivatization, coupling, thiab koom ua ke rau hauv cov molecules complex. Nws ruaj khov nyob rau hauv cov txheej txheem khaws cia thiab cov tshuaj tiv thaiv ua kom muaj txiaj ntsig zoo hauv ob qho tib si kev sim thiab kev siv tshuab. Qhov sib xyaw ua ke nrog cov organic synthesis reagents thiab kev tiv thaiv-pab cov tswv yim txhim kho kev ua tau zoo, yields, thiab kev xaiv hauv ntau txoj hauv kev hluavtaws.