(1S,2S)-2-(3-bromophenyl)cyclopropanecarboxylic acid CAS: 2165565-11-5
(1S,2S)-2-(3-bromophenyl)cyclopropanecarboxylic acid muaj kev cia siab hauv kev kho mob tshuaj ua lub hauv paus 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 ntsuas nws qhov kev ntshiab enantiomeric thiab kawm nws cov kev sib cuam tshuam nrog cov kab mob hauv lub cev los ntsuas nws lub peev xwm kho mob. Lub compound's chiral xwm yuav raug siv los tsim cov neeg sawv cev tshuaj xaiv nrog kev ua tau zoo dua thiab txo cov kev phiv. Hauv kev tsim cov organic, cov compound no tuaj yeem ua haujlwm ua lub hauv paus tseem ceeb rau kev nkag mus rau cov qauv sib txawv los ntawm kev hloov pauv asymmetric lossis derivatization reactions. Nws kev koom ua ke rau hauv cov txheej txheem synthetic tso cai rau kev tsim cov qauv molecular nyuaj rau kev kawm txog kev sib raug zoo ntawm cov qauv-kev ua ub no lossis tsim cov tshuaj tshiab nrog cov khoom tshwj xeeb. Los ntawm kev siv nws cov stereochemistry thiab reactivity, cov kws tshawb fawb tuaj yeem txhim kho cov txheej txheem synthetic thiab pab txhawb rau kev tsim cov tshuaj tshiab rau ntau yam kev siv scientific thiab industrial. Zuag qhia tag nrho, (1S,2S)-2-(3-bromophenyl)cyclopropanecarboxylic acid qhia txog kev ua tau ntau yam thiab muaj peev xwm hauv kev txhim kho kev tshawb nrhiav tshuaj, kev siv zog tsim cov organic, thiab kev tsim kho tshiab hauv tshuaj, qhia txog nws qhov tseem ceeb hauv kev txhawb nqa kev paub txog kev tshawb fawb thiab kev nce qib hauv kev lag luam tshuaj.
| Kev sau ua ke | C10H9BrO2 |
| Kev Ntsuas | 99% |
| Qhov tsos | hmoov dawb |
| CAS Nr. | 2165565-11-5 |
| Ntim khoom | Me me thiab ntau |
| Lub Neej Txee | 2 xyoos |
| Kev Khaws Cia | Khaws cia rau qhov chaw txias thiab qhuav |
| Daim Ntawv Pov Thawj | ISO. |








