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(4S)-3-[(5R)-5-(4-FLUOROPHENYL)-5-HYDROXYPENTANOYL]-4-PHENYL-1,3-OXAZOLIDIN-2-ONE CAS: 189028-95-3
(4S)-3-[(5R)-5-(4-FLUOROPHENYL)-5-HYDROXYPENTANOYL]-4-PHENYL-1,3-OXAZOLIDIN-2-ONE yog ib qho tshuaj lom neeg uas yog oxazolidinone chav kawm, uas muaj nws cov qauv nyuaj thiab kev cuam tshuam rau tshuaj. Cov tshuaj no yog qhov tseem ceeb rau nws cov chirality thiab muaj ib pawg phenyl txuas rau 1,3-oxazolidin-2-ib lub nplhaib system. Qhov muaj ib pawg fluorophenyl thiab ib pawg hydroxypentanoyl muab cov khoom siv tshuaj tshwj xeeb uas tseem ceeb rau nws cov haujlwm biological thiab cov ntawv thov kho mob. Synthesized los ntawm cov txheej txheem tshwj xeeb, qhov oxazolidinone derivative no qhia txog cov khoom lag luam pharmacological zoo, ua rau nws yog ib qho kev txaus siab rau kev kho mob tshuaj thiab kev tsim tshuaj.
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2-[2-(2-Fluorophenyl)-2-oxoethyl]propanedinitrile CAS: 312307-38-3
2-[2-(2-Fluorophenyl)-2-oxoethyl]propanedinitrile yog ib qho tshuaj lom neeg uas paub txog nws cov qauv molecular nyuaj, uas muaj cov pob txha caj qaum propanedinitrile hloov nrog 2-fluorophenyl pawg txuas rau 2-oxoethyl moiety. Qhov kev npaj no ua rau muaj cov khoom siv tshuaj tshwj xeeb uas tseem ceeb hauv ntau qhov chaw tshawb fawb, tshwj xeeb tshaj yog tshuaj lom neeg thiab kev tshawb fawb txog khoom siv. Siv cov txheej txheem tshuaj lom neeg tshwj xeeb, cov tshuaj no ua lub hauv paus tseem ceeb rau kev tsim cov tshuaj thiab cov ntaub ntawv ua haujlwm, siv nws cov yam ntxwv tshwj xeeb thiab kev ua haujlwm.
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O,O'-di-tert-butyl-L-threonine acetate CAS: 5854-77-3
O,O'-di-tert-butyl-L-threonine acetate yog ib qho tshuaj lom neeg uas muaj npe nrov rau nws cov qauv molecular, uas suav nrog threonine backbone hloov nrog ob pawg tert-butyl thiab ib qho acetate moiety. Cov tshuaj no tseem ceeb hauv cov organic chemistry vim nws cov stereochemistry tshwj xeeb thiab cov ntawv thov muaj peev xwm hauv kev tshawb fawb txog tshuaj thiab biochemical. Synthesized los ntawm cov txheej txheem tshwj xeeb organic synthesis, O,O'-di-tert-butyl-L-threonine acetate ua haujlwm ua lub tsev thaiv ntau yam thiab nruab nrab hauv kev tsim cov tshuaj tshiab thiab cov tshuaj biochemical probes.
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4-fluoro-2-Methoxy-5-nitroaniline CAS: 1421372-66-8
4-Fluoro-2-methoxy-5-nitroaniline yog ib qho tshuaj lom neeg uas paub txog nws cov qauv aromatic uas muaj ib pawg nitro, ib pawg fluoro substituent, thiab ib pawg methoxy txuas rau ib lub nplhaib aniline. Qhov kev teeb tsa no muab nws cov khoom siv tshuaj lom neeg tshwj xeeb uas tsim nyog rau ntau yam kev siv hauv kev tsim cov organic thiab kev tshawb fawb txog tshuaj. Tsim los ntawm cov txheej txheem organic chemistry, cov tshuaj no ua haujlwm ua lub hauv paus tseem ceeb rau kev tsim cov ntaub ntawv tshwj xeeb thiab cov tshuaj nruab nrab, siv nws cov yam ntxwv tshwj xeeb.
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4-(4-Fluorobenzoyl)butyric acid CAS: 149437-76-3
4-(4-Fluorobenzoyl)butyric acid yog ib yam tshuaj lom neeg uas paub txog nws cov qauv uas muaj cov butyric acid backbone nrog 4-(4-fluorobenzoyl) substituent. Cov tshuaj no yog qhov tseem ceeb hauv cov organic chemistry rau nws cov kev siv hauv kev lag luam tshuaj thiab cov ntaub ntawv tshawb fawb. Qhov muaj cov pab pawg fluorobenzoyl hloov nws cov khoom siv tshuaj, cuam tshuam rau nws cov solubility, reactivity, thiab cov haujlwm biological. Synthesized los ntawm cov txheej txheem organic synthesis, 4-(4-fluorobenzoyl)butyric acid ua haujlwm ua tus precursor lossis nruab nrab hauv kev tsim cov neeg sawv cev kho mob thiab cov ntaub ntawv ua haujlwm.
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4-[[(4-Fluorophenyl)imino]methyl]-phenol CAS: 3382-63-6
4-[[(4-Fluorophenyl)imino]methyl]-phenol yog ib yam tshuaj sib xyaw uas txawv ntawm nws cov qauv molecular, uas muaj lub nplhaib phenolic txuas rau 4-fluorophenyl imine pawg. Qhov kev teeb tsa no muab cov tshuaj sib xyaw nrog cov khoom siv tshuaj tshwj xeeb uas tseem ceeb hauv kev siv tshuaj thiab kev lag luam. Tsim los ntawm cov txheej txheem tshuaj lom neeg tshwj xeeb, cov tshuaj no ua haujlwm ua lub hauv paus rau kev tsim cov tshuaj thiab cov ntaub ntawv ua haujlwm, vim nws cov qauv sib txawv thiab kev ua haujlwm.
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(4S)-3-[5-(4-Fluorophenyl)-1,5-dioxopenyl]-4-phenyl-2-oxazolidinone CAS: 189028-93-1
(4S)-3-[5-(4-Fluorophenyl)-1,5-dioxopenyl]-4-phenyl-2-oxazolidinone yog ib yam tshuaj uas yog ib feem ntawm pawg oxazolidinone, uas txawv ntawm nws qhov nyuaj ntawm cov qauv thiab kev cuam tshuam ntawm cov tshuaj. Cov tshuaj no muaj ib lub chaw chiral ntawm 4-txoj haujlwm ntawm lub nplhaib oxazolidinone, uas hu ua 4S, uas ua lub luag haujlwm tseem ceeb hauv nws cov haujlwm thiab kev sib cuam tshuam ntawm cov tshuaj lom neeg. Qhov muaj ib pawg 4-fluorophenyl txuas nrog 1,5-dioxopenyl moiety ua rau nws cov khoom siv tshuaj zoo dua, ua rau nws yog ib qho kev txaus siab rau kev kho mob thiab kev tsim tshuaj.
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Diethyl ethylmalonate CAS: 133-13-1
Diethyl ethylmalonate yog ib hom tshuaj uas muaj cov mis molecular C8H14O4. Nws yog ib hom tshuaj malonic acid derivatives thiab muaj ob pawg ethyl txuas rau malonate moiety. Cov tshuaj no paub txog nws qhov kev ua tau zoo hauv kev tsim cov organic.
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(2S,5R)-Methyl-5-[(benzyloxy)amino]piperidine-2-carboxylate ethanedioate CAS: 1416134-48-9
(2S,5R)-Methyl-5-[(benzyloxy)amino]piperidine-2-carboxylate ethanedioate yog ib qho tshuaj sib xyaw nrog cov mis molecular C16H22N2O6. Nws yog ib feem ntawm cov piperidine derivatives thiab muaj cov methylated piperidine core nrog cov benzyloxyamino substituent thiab ethanedioate counterions. Cov tshuaj no yog qhov tseem ceeb rau nws qhov nyuaj ntawm cov qauv thiab cov khoom siv tshuaj tshwj xeeb.
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(R)-4-phenyl-2-oxazolidinone CAS: 90319-52-1
(R)-4-Phenyl-2-oxazolidinone, tseem hu ua S-Phenyloxazolidinone, yog ib qho tshuaj lom neeg uas muaj cov mis molecular C9H9NO2. Nws feem ntau yog siv ua chiral auxiliary hauv asymmetric synthesis vim nws muaj peev xwm cuam tshuam rau stereochemistry thaum lub sijhawm tshuaj tiv thaiv.
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(S)-4-phenyl-2-oxazolidinone CAS: 99395-88-7
(S)-4-Phenyl-2-oxazolidinone, tseem hu ua R-Phenyloxazolidinone, yog ib qho tshuaj lom neeg uas muaj cov mis molecular C9H9NO2. Nws yog siv los ua chiral auxiliary hauv asymmetric synthesis vim nws muaj peev xwm cuam tshuam rau stereochemistry ntawm cov tshuaj tiv thaiv.
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P-methoxy phenylacetone CAS: 122-84-9
P-Methoxy phenylacetone, tseem hu ua 1-(4-Methoxyphenyl)-2-propanone, yog ib qho tshuaj sib xyaw nrog cov mis molecular C10H12O2. Nws yog ib qho aromatic ketone uas muaj ib pawg methoxy txuas rau lub nplhaib phenyl. Cov tshuaj sib xyaw no yog siv rau hauv ntau yam tshuaj syntheses thiab kev siv tshuaj.
