tert-butyl (1R, 2S)-2-(3-bromophenyl)cyclopropylcarbamate CAS: 1314323-97-1

tert-butyl (1R,2S)-2-(3-bromophenyl)cyclopropylcarbamate siv tau rau hauv kev tshawb fawb txog tshuaj lom neeg ua ib qho tseem ceeb rau kev tsim cov tshuaj uas muaj peev xwm tsom mus rau cov kab mob tshwj xeeb lossis cov hom phiaj molecular. Cov kws tshawb fawb tuaj yeem tshawb nrhiav nws cov khoom pharmacological los ntawm kev soj ntsuam nws cov kev sib cuam tshuam nrog cov enzymes, receptors, lossis cov txheej txheem cellular los ntsuas nws cov peev xwm kho mob. Lub compound's chiral xwm yuav siv tau los tsim cov tshuaj enantiomerically ntshiab nrog kev txhim kho bioactivity thiab txo cov teebmeem tawm ntawm lub hom phiaj. Hauv kev tsim cov organic, cov tshuaj no ua haujlwm ua lub tsev thaiv ntau yam rau kev nkag mus rau cov qauv sib txawv los ntawm kev derivatization lossis stereoselective transformations. Nws suav nrog hauv cov kev tsim ua rau muaj 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 ntau yam kev siv scientific thiab industrial. Zuag qhia tag nrho, tert-butyl (1R, 2S) -2- (3-bromophenyl) cyclopropylcarbamate qhia txog kev ua tau zoo thiab kev cog lus hauv kev tshawb pom tshuaj, kev tsim cov organic, thiab kev tsim kho tshiab hauv tshuaj, qhia txog nws qhov tseem ceeb hauv kev txhim kho kev paub txog kev tshawb fawb thiab kev nce qib hauv kev lag luam tshuaj.