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(R)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid CAS: 1263077-92-4
(R)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid yog ib qho tshuaj muaj nqis uas muaj txiaj ntsig zoo hauv kev tsim cov organic thiab kev tshawb fawb txog tshuaj. Nws lub hauv paus chiral morpholine, uas muaj pawg tiv thaiv tert-butoxycarbonyl (Boc) ntawm 4-txoj haujlwm thiab kev ua haujlwm carboxylic acid ntawm 3-txoj haujlwm, muab cov khoom tshwj xeeb stereochemical thiab reactivity. Cov molecule no ua haujlwm ua ib qho tseem ceeb rau kev tsim cov chiral building blocks thiab cov tshuaj intermediates, ua rau kev tsim cov qauv molecular nyuaj nrog cov stereochemistry txhais. Cov kws tshawb fawb thiab cov kws tshuaj siv cov tshuaj no los pab txhawb kev tsim cov tshuaj asymmetric thiab nkag mus rau cov tshuaj enantiomerically ntshiab rau kev tshawb pom tshuaj thiab cov ntaub ntawv siv science.
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(1H-Indol-3-yl) acetaldoxime CAS: 2776-06-9
(1H-Indol-3-yl)acetaldoxime yog ib qho tshuaj lom neeg tseem ceeb uas muaj ntau yam kev siv hauv kev tsim cov organic thiab tshuaj lom neeg biology. Cov oxime derivative no muaj lub nplhaib indole txuas nrog rau acetaldoxime moiety, sib xyaw cov khoom aromatic nrog oxime functionality. Qhov muaj nyob ntawm indole scaffold muab cov yam ntxwv hluav taws xob thiab cov qauv sib txawv, ua rau cov tshuaj no muaj txiaj ntsig zoo rau ntau yam kev hloov pauv synthetic thiab kev tshawb fawb txog tsiaj txhu. (1H-Indol-3-yl)acetaldoxime ua haujlwm ua lub tsev thaiv rau kev tsim cov tshuaj heterocyclic thiab molecular probes, muab cov sijhawm rau kev tsim qauv molecular tshiab thiab kev tshawb nrhiav hauv kev tshawb fawb txog tshuaj lom neeg.
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(3S,4S)-1-Benzyl-4-(hydroxymethyl)pyrrolidin-3-ol CAS: 849935-80-4
(3S,4S)-1-Benzyl-4-(hydroxymethyl)pyrrolidin-3-ol yog ib qho tshuaj lom neeg tseem ceeb nrog ntau yam kev siv hauv kev tsim cov organic thiab tshuaj lom neeg. Lub stereochemistry ntawm cov pyrrolidine derivative no, uas muaj (3S,4S) configuration, txhais nws cov qauv tshwj xeeb thiab cov khoom ua haujlwm. Pawg benzyl ntawm 1-txoj haujlwm thiab hydroxymethyl moiety ntawm 4-txoj haujlwm pab txhawb rau nws cov khoom siv ntau yam thiab kev ua haujlwm ntau yam. Cov tshuaj no ua haujlwm ua lub hauv paus tseem ceeb rau kev tsim cov tshuaj molecules nyuaj thiab cov tshuaj intermediates, muab cov sijhawm rau kev tsim cov tshuaj molecular tshiab thiab kev tshawb nrhiav hauv kev tshawb fawb tshuaj lom neeg.
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(R)-6,6-Dimethyl-morpholine-3-carboxylic acid hydrochloride CAS: 1313277-22-3
(R)-6,6-Dimethyl-morpholine-3-carboxylic acid hydrochloride yog ib qho tshuaj lom neeg tseem ceeb uas siv rau hauv kev tsim tshuaj thiab cov organic synthesis. Qhov kev teeb tsa (R) enantiomer ntawm cov morpholine derivative no ua kom nws cov stereochemistry meej, ua rau nws muaj txiaj ntsig zoo rau kev siv chiral. Nws cov ntsev hydrochloride ua rau nws cov solubility thiab kev ruaj khov, ua rau nws siv tau ntau yam kev cuam tshuam. Cov tshuaj no ua haujlwm ua lub hauv paus tseem ceeb rau kev tsim cov chiral molecules nrog cov haujlwm tshwj xeeb thiab cov khoom siv, muab kev hloov pauv thiab kev ntseeg tau hauv kev hloov pauv tshuaj lom neeg.
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(R)-N-methyl(pyrrolidin-2-yl)methanamine dihydrochloride CAS: 119020-04-1
(R)-N-methyl(pyrrolidin-2-yl)methanamine dihydrochloride yog ib qho tshuaj lom neeg siv dav hauv kev tshawb fawb thiab kev txhim kho tshuaj. Cov ntsev dihydrochloride no yog los ntawm N-methyl(pyrrolidin-2-yl)methanamine uas muaj nqis rau nws qhov kev ruaj khov thiab kev yaj zoo dua li cov qauv dawb. Nrog rau cov qauv chiral thiab cov qauv molecular tshwj xeeb, (R)-N-methyl(pyrrolidin-2-yl)methanamine dihydrochloride ua haujlwm ua ib qho tseem ceeb hauv kev tsim cov tshuaj thiab cov tshuaj bioactive.
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(R)-Methyl6,6-dimethylmorpholine-3-carboxylate hydrochloride CAS: 1313278-08-8
(R)-Methyl 6,6-dimethylmorpholine-3-carboxylate hydrochloride yog ib qho tshuaj muaj txiaj ntsig siv rau hauv kev tsim cov organic thiab kev tshawb fawb txog tshuaj. Cov chiral morpholine derivative no muaj cov methyl ester functionality ntawm 3-position, muab cov reactivity tshwj xeeb thiab cov khoom stereochemical. Cov ntsev hydrochloride ua rau nws ruaj khov thiab solubility, ua rau nws yog ib qho reagent yooj yim rau ntau yam kev hloov pauv synthetic. Cov kws tshuaj thiab cov kws tshawb fawb siv cov tshuaj no ua ib qho tseem ceeb rau kev npaj cov chiral building blocks thiab cov tshuaj intermediates, ua rau muaj kev sib xyaw ntawm cov enantiomerically pure compounds rau kev tshawb pom tshuaj thiab cov ntaub ntawv siv science.
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(R)-5-phenylpyrrolidin-2-ib CAS: 313352-62-4
(R)-5-phenylpyrrolidin-2-ib yog ib qho tshuaj lom neeg tseem ceeb uas siv rau hauv kev tsim cov organic thiab tshuaj lom neeg. Cov molecule chiral no muaj ib lub nplhaib pyrrolidin-2-ib nrog ib pawg phenyl txuas rau hauv 5-txoj haujlwm, muab cov khoom tshwj xeeb stereochemical thiab cov qauv tsim uas haum rau ntau yam kev hloov pauv tshuaj. Qhov (R)-configuration ua kom muaj stereochemistry tshwj xeeb, ua rau nws muaj txiaj ntsig zoo rau kev siv chiral thiab asymmetric synthesis. Cov tshuaj no ua haujlwm ua lub hauv paus tseem ceeb rau kev npaj cov chiral intermediates thiab tshuaj, muab cov sijhawm rau kev tsim qauv molecular tshiab thiab kev tshawb nrhiav hauv kev tshawb fawb tshuaj lom neeg.
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(1R,2S)-2-(3-bromophenyl)cyclopropanamine hydrochloride CAS: 1314324-03-2
(1R,2S)-2-(3-bromophenyl)cyclopropanamine hydrochloride yog ib qho tshuaj siv hauv kev tshawb fawb thiab kev txhim kho tshuaj. Nws yog ib feem ntawm cov chav kawm ntawm cyclopropane derivatives thiab nws yog tus cwj pwm los ntawm nws cov stereochemistry tshwj xeeb thiab kev npaj pawg ua haujlwm. Cov tshuaj no yog synthesized rau nws cov ntawv thov hauv kev kho mob vim nws cov qauv molecular nthuav thiab reactivity. Nrog kev ntshiab siab thiab kev ruaj khov, (1R,2S)-2-(3-bromophenyl)cyclopropanamine hydrochloride ua haujlwm ua lub hauv paus tseem ceeb hauv kev tsim cov tshuaj tshiab thiab cov tshuaj bioactive.
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(R)-N-methyl(pyrrolidin-2-yl)methanamine CAS: 68766-97-2
(R)-N-methyl(pyrrolidin-2-yl)methanamine yog ib qho tshuaj lom neeg uas feem ntau siv rau hauv kev tshawb fawb txog tshuaj thiab kev tsim cov organic. Nws yog ib feem ntawm N-methylated pyrrolidine derivatives thiab nws yog tus cwj pwm los ntawm nws cov yam ntxwv chiral thiab cov qauv molecular tshwj xeeb. Cov tshuaj no muaj nqis rau nws cov haujlwm pharmacological thiab ntau yam kev ua haujlwm hauv kev hloov pauv tshuaj. Nrog kev ntshiab siab thiab kev ruaj khov, (R)-N-methyl(pyrrolidin-2-yl)methanamine ua haujlwm ua lub hauv paus tseem ceeb hauv kev tsim cov tshuaj lom neeg thiab cov neeg sib tw tshuaj.
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4-Fluorothiophenol CAS: 371-42-6
4-Fluorothiophenol yog ib hom tshuaj uas muaj cov mis molecular C6H5FS. Nws muaj ib lub fluorine atom uas txuas nrog lub nplhaib thiophenol ntawm qhov chaw thib 4. Paub txog nws cov qauv tshuaj thiab cov khoom sib txawv, 4-Fluorothiophenol pom cov ntawv thov hauv ntau yam lag luam vim nws cov tshuaj tiv thaiv thiab kev hloov pauv tau yooj yim.
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Phenylsulfide CAS: 139-66-2
Phenylsulfide, nrog rau cov tshuaj mis C6H5S, yog ib qho tshuaj uas muaj pawg phenyl sib txuas nrog ib lub atom sulfur. Kuj tseem hu ua benzene sulfide, nws yog tus cwj pwm los ntawm nws cov qauv aromatic thiab cov khoom siv tshuaj lom neeg sib txawv. Phenylsulfide pom kev siv hauv ntau yam lag luam vim nws qhov kev hloov pauv tau thiab kev ua haujlwm.
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Thioanisole CAS: 100-68-5
Thioanisole yog ib hom tshuaj uas muaj cov mis molecular C7H8S. Nws yog tus cwj pwm los ntawm ib lub atom sulfur txuas rau ib lub nplhaib aromatic, qhia txog cov khoom aromatic thiab reactivity tshwj xeeb. Thioanisole ua haujlwm ua lub hauv paus rau kev tsim cov organic vim nws cov yam ntxwv ntawm cov qauv thiab cov pab pawg ua haujlwm.
