Methyl 4-amino-3-bromobenenzoate 丨 cas 106896-49-5

Methylat 4 - Am1 {}}}}}} 3-bromobenlen intermedocical thiab tshuaj synthesis. Nws cov ntaub ntawv tseem ceeb yog lub tsev thaiv kev npaj ntawm cov khoom xyaw ua tshuaj (APIs), heterocyclic tebchaw, thiab zoo tshuaj. Cov molecule muaj ob qho amino pab pawg thiab lub bromine hloov pauv ntawm cov yeeb yaj kiab uas ntxhiab tsw xws li nucleophilic hloov, sib txuas-coupling cov kev tawm tsam, thiab kev hla kev. Qhov no ua rau nws tshwj xeeb tshwj xeeb hauv kev ua ke lom zem rau kev sib txuas, suav nrog kev ua haujlwm nruab nrab rau cov neeg sawv cev, thiab cov tshuaj tiv thaiv antimicrobial. Nws tus ester ua haujlwm ntxiv rau kev xaiv kev hloov kho lossis kev sib txuam rau hauv cov txheej txheem molecular.

Cov txiaj ntsig ntawm methyl 4 - amino-3-bromobenenzoate qia los ntawm nws cov khoom siv tshuaj thiab reactivity. Cov amino thiab bromine pawg muab ntau qhov chaw rau kev tsom xam cov haujlwm, muab cov khoom siv hluav taws xob muaj txiaj ntsig nrog cov kev xaiv siab thiab tawm los. Hauv cov khoom siv hluav taws xob synthesis, nws ua rau kev tsim cov nruab nrab uas tseem ceeb heev rau kev tsim cov tshuaj nrog kev kho mob tshwj xeeb. Nws cov pab pawg Es ester tso cai rau cov tswv yim ntxiv lossis tiv thaiv kev tiv thaiv, nce kev hloov pauv hauv multistep syntheses. Ib qho ntxiv, nws ruaj khov thiab muaj kev huv ua rau nws haum rau ob qho kev lag luam kev lag luam thiab kev lag luam txhim khu kev txhim khu kev qha thiab rov ua kom tau zoo.